Autoimmune encephalitis in a resource-limited public health setting: a case series analysis
Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic pr...
Saved in:
Published in | Arquivos de neuro-psiquiatria Vol. 82; no. 2; pp. 1 - 10 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Arquivos de Neuro-Psiquiatria
01.02.2024
Thieme Revinter Publicações Ltda Academia Brasileira de Neurologia - ABNEURO Thieme Revinter Publicações |
Subjects | |
Online Access | Get full text |
ISSN | 0004-282X 1678-4227 1678-4227 |
DOI | 10.1055/s-0044-1779054 |
Cover
Abstract | Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies.
Objective To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes.
Methods We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality.
Results Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up.
Conclusion In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. |
---|---|
AbstractList | Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies.BACKGROUND Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes.OBJECTIVE To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes. We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality.METHODS We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality. Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up.RESULTS Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up. In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies.CONCLUSION In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. Objective To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes. Methods We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality. Results Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up. Conclusion In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. Objective To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes. Methods We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality. Results Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up. Conclusion In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. Objective To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes. Methods We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality. Results Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up. Conclusion In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. Abstract Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. Objective To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes. Methods We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality. Results Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up. Conclusion In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the onset. Due to the heterogeneity of clinical presentations, it is difficult to achieve uniformity for the diagnostic and therapeutic processes and follow-up strategies. To describe a series of patients diagnosed with AE in a resource-limited public hospital in southern Brazil and to analyze therapeutics and outcomes. We retrospectively reviewed the electronic medical records of patients diagnosed with AE at the Hospital de Clínicas de Porto Alegre from 2014 to 2022. Data collected included clinical presentation, neuroimaging, cerebrospinal fluid testings, electroencephalogram, autoantibodies, treatments, outcomes, follow-up time, degree of neurological impairment, and mortality. Data from 17 patients were retrieved. Eleven cases were classified as definite AE and 6 as possible AE. Autoantibodies were identified in 9 patients. Timing for diagnosis was impacted by the high costs associated with autoantibody testing. Most patients became functionally dependent (82.4%) and most survivors remained with autoimmune-associated epilepsy (75%). Five patients died during hospitalization, and one after a 26-month of follow-up. In this resource-limited hospital, patients with AE had a worse clinical outcome than that previously described in the literature. Development of epilepsy during follow-up and mortality were greater, whilst functional outcome was inferior. Autoantibody testing was initially denied in most patients, which impacted the definitive diagnosis and the use of second-line therapies. |
Author | Noll, Giovani Leite, Martim Bravo Bianchin, Marino Muxfeldt Torres, Carolina Machado Piccini, Cristian Daniel Castilhos, Raphael Machado Borelli, Wyllians Vendramini Morillos, Matheus Bernardon Finkelsztejn, Alessandro |
AuthorAffiliation | 2 Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Porto Alegre RS, Brazil 3 Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Departamento de Medicina Interna, Porto Alegre RS, Brazil 1 Hospital de Clínicas de Porto Alegre, Serviço de Neurologia, Porto Alegre RS, Brazil 4 Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Programa de Pós-Graduação em Medicina: Ciências Médicas, Porto Alegre RS, Brazil |
AuthorAffiliation_xml | – name: 3 Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Departamento de Medicina Interna, Porto Alegre RS, Brazil – name: 4 Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Programa de Pós-Graduação em Medicina: Ciências Médicas, Porto Alegre RS, Brazil – name: 2 Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Porto Alegre RS, Brazil – name: 1 Hospital de Clínicas de Porto Alegre, Serviço de Neurologia, Porto Alegre RS, Brazil – name: Universidade Federal do Rio Grande do Sul – name: Hospital de Clínicas de Porto Alegre |
Author_xml | – sequence: 1 givenname: Matheus Bernardon orcidid: 0000-0002-1091-1495 surname: Morillos fullname: Morillos, Matheus Bernardon – sequence: 2 givenname: Wyllians Vendramini orcidid: 0000-0001-9282-0601 surname: Borelli fullname: Borelli, Wyllians Vendramini – sequence: 3 givenname: Giovani orcidid: 0000-0002-9484-8365 surname: Noll fullname: Noll, Giovani – sequence: 4 givenname: Cristian Daniel orcidid: 0000-0003-4720-4601 surname: Piccini fullname: Piccini, Cristian Daniel – sequence: 5 givenname: Martim Bravo orcidid: 0000-0002-0824-9308 surname: Leite fullname: Leite, Martim Bravo – sequence: 6 givenname: Alessandro orcidid: 0000-0002-2856-1200 surname: Finkelsztejn fullname: Finkelsztejn, Alessandro – sequence: 7 givenname: Marino Muxfeldt orcidid: 0000-0001-8345-6713 surname: Bianchin fullname: Bianchin, Marino Muxfeldt – sequence: 8 givenname: Raphael Machado orcidid: 0000-0002-1905-2084 surname: Castilhos fullname: Castilhos, Raphael Machado – sequence: 9 givenname: Carolina Machado orcidid: 0000-0003-0562-9513 surname: Torres fullname: Torres, Carolina Machado |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38325385$$D View this record in MEDLINE/PubMed |
BookMark | eNp1UkuLFDEYDLLizo5ePUqDFy-95tV5eJFl8bGw4EEFwUNI0umZDOnOmKSF_femnXF0FwyB8CVVRdWX7wKcTXFyADxH8BLBrnudWwgpbRHnEnb0EVghxkVLMeZnYAXrW4sF_nYOLnLeQYiplPwJOCeC4I6IbgW-X80l-nGcJ9e4ybr9VgdffG781OgmuRznZF0b_OiL65v9bIK3zdbpULZNdqX4afOmIq3OrtbJu9zoSYe77PNT8HjQIbtnx3MNvr5_9-X6Y3v76cPN9dVtazuGS8t70RtpsLCDtoZSZolhkskaghLWGWQHJIzB2GBIOs4FknUxCZ0xHWeGrMHNQbePeqf2yY863amovfp9EdNG6VS8DU4hg5kVmnBdxQWhBhLBetwjPnS90X3VujxoZetdiGpX89c4WX1emqmWZuLaxlrgZaNKeHsg1NaMrrduKkmHey7uv0x-qzbxp0JQUCnqN6zBq6NCij9ml4safbYuBD25OGeFJSYSUUh4hb58AD35I5BgVg0hWVEv_rV08vLn1_-GtCnmnNxwgiColrFSWS1jpY5jVQn0AcH6oouPSyQf_kf7BafszRc |
CitedBy_id | crossref_primary_10_1055_s_0044_1781442 crossref_primary_10_1016_j_eplepsyres_2024_107439 |
Cites_doi | 10.1016/j.clinimag.2021.12.011 10.1111/ane.12791 10.4103/aian.AIAN_817_20 10.1097/MD.0000000000019601 10.1038/s41380-021-01396-4 10.1212/NXI.0000000000000633 10.3389/fimmu.2021.691536 10.1212/WNL.0b013e3182a4a49c 10.3389/fimmu.2022.890656 10.1126/science.1223466 10.1016/j.yebeh.2018.10.038 10.1093/qjmed/hcr111 10.3389/fneur.2021.673339 10.1371/journal.pone.0146455 10.1136/jnnp-2020-325300 10.1007/s00415-020-09807-2 10.1111/epi.13929 10.1093/brain/awh203 10.1212/NXI.0000000000000514 10.1097/WCO.0000000000001050 10.1016/S1474-4422(15)00401-9 10.3390/ijms21103701 10.1002/ana.25131 10.1186/1752-1947-7-223 10.1177/1941874420987053 10.1111/1468-0009.12530 10.1016/j.seizure.2017.05.017 10.1002/jca.21363 10.1111/ane.12575 10.1136/jnnp.2006.100644 10.1016/j.seizure.2020.07.019 10.1016/j.autneu.2015.08.002 10.3389/fneur.2022.788309 10.1111/epi.16571 10.1016/S1474-4422(08)70224-2 10.3389/fneur.2020.606350 10.1016/j.jaut.2018.10.014 |
ContentType | Journal Article |
Copyright | The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/). Copyright Arquivos de Neuro-Psiquiatria Feb 2024 The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit ( ) 2024 The Author(s). This work is licensed under a Creative Commons Attribution 4.0 International License. |
Copyright_xml | – notice: The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/). – notice: Copyright Arquivos de Neuro-Psiquiatria Feb 2024 – notice: The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit ( ) 2024 The Author(s). – notice: This work is licensed under a Creative Commons Attribution 4.0 International License. |
DBID | AAYXX CITATION NPM 7TK 8FD FR3 P64 RC3 7X8 5PM GPN DOA |
DOI | 10.1055/s-0044-1779054 |
DatabaseName | CrossRef PubMed Neurosciences Abstracts Technology Research Database Engineering Research Database Biotechnology and BioEngineering Abstracts Genetics Abstracts MEDLINE - Academic PubMed Central (Full Participant titles) SciELO DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed Genetics Abstracts Engineering Research Database Technology Research Database Neurosciences Abstracts Biotechnology and BioEngineering Abstracts MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic CrossRef Genetics Abstracts PubMed |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Public Health |
DocumentTitleAlternate | Encefalite autoimune em um hospital universitário público: análise de uma série de casos |
EISSN | 1678-4227 |
EndPage | 10 |
ExternalDocumentID | oai_doaj_org_article_1b26c8a37a224834b0386d2d17f5dbad S0004_282X2024000200201 PMC10849825 38325385 10_1055_s_0044_1779054 |
Genre | Journal Article |
GroupedDBID | --- .GJ 0R~ 0U6 23N 2WC 53G 5GY 5VS 6J9 AAFWJ AAYXX ABIVO ABXHO ADBBV AENEX AFPKN AHRAW ALMA_UNASSIGNED_HOLDINGS APOWU AZFZN BAWUL BCNDV C1A CITATION CS3 DIK E3Z EBS EJD F5P GROUPED_DOAJ GX1 IPNFZ KQ8 KWQ OK1 OVT P2P PGMZT RIG RNS RPM RSC RTC SCD XSB NPM 7TK 8FD FR3 P64 RC3 7X8 5PM GPN |
ID | FETCH-LOGICAL-c562t-7d8db9b28cfacb446c3b69694224365b1cf18bb22b203577819999690ebb576b3 |
IEDL.DBID | DOA |
ISSN | 0004-282X 1678-4227 |
IngestDate | Wed Aug 27 01:31:57 EDT 2025 Tue Sep 16 20:57:09 EDT 2025 Thu Aug 21 18:35:19 EDT 2025 Fri Jul 11 05:35:12 EDT 2025 Mon Jun 30 06:48:26 EDT 2025 Mon Jul 21 06:00:34 EDT 2025 Tue Jul 01 02:04:54 EDT 2025 Thu Apr 24 23:12:58 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | Autoanticorpos Autoantibodies Síndromes Paraneoplásicas do Sistema Nervoso Encefalite Límbica Paraneoplastic Syndromes, Nervous System Limbic Encephalitis Convulsões Seizures |
Language | English |
License | https://creativecommons.org/licenses/by/4.0 The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/). This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This work is licensed under a Creative Commons Attribution 4.0 International License. http://creativecommons.org/licenses/by/4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c562t-7d8db9b28cfacb446c3b69694224365b1cf18bb22b203577819999690ebb576b3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0001-8345-6713 0000-0001-9282-0601 0000-0002-9484-8365 0000-0002-1905-2084 0000-0002-1091-1495 0000-0003-4720-4601 0000-0002-2856-1200 0000-0002-0824-9308 0000-0003-0562-9513 |
OpenAccessLink | https://doaj.org/article/1b26c8a37a224834b0386d2d17f5dbad |
PMID | 38325385 |
PQID | 3032620119 |
PQPubID | 2049055 |
PageCount | 10 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_1b26c8a37a224834b0386d2d17f5dbad scielo_journals_S0004_282X2024000200201 pubmedcentral_primary_oai_pubmedcentral_nih_gov_10849825 proquest_miscellaneous_2923914037 proquest_journals_3032620119 pubmed_primary_38325385 crossref_primary_10_1055_s_0044_1779054 crossref_citationtrail_10_1055_s_0044_1779054 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2024-02-01 |
PublicationDateYYYYMMDD | 2024-02-01 |
PublicationDate_xml | – month: 02 year: 2024 text: 2024-02-01 day: 01 |
PublicationDecade | 2020 |
PublicationPlace | Germany |
PublicationPlace_xml | – name: Germany – name: Sao Paulo – name: Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil |
PublicationTitle | Arquivos de neuro-psiquiatria |
PublicationTitleAlternate | Arq Neuropsiquiatr |
PublicationYear | 2024 |
Publisher | Arquivos de Neuro-Psiquiatria Thieme Revinter Publicações Ltda Academia Brasileira de Neurologia - ABNEURO Thieme Revinter Publicações |
Publisher_xml | – name: Arquivos de Neuro-Psiquiatria – name: Thieme Revinter Publicações Ltda – name: Academia Brasileira de Neurologia - ABNEURO – name: Thieme Revinter Publicações |
References | K Herard (ref17) 2019; 11 M Dade (ref19) 2020; 21 W Zhang (ref24) 2019; 94 X Chi (ref14) 2017; 136 J Dalmau (ref34) 2008; 7 D Endres (ref3) 2022; 27 R Ruiz-García (ref6) 2021; 12 M Falip (ref31) 2020; 81 S Aurangzeb (ref35) 2017; 50 T Wingfield (ref9) 2011; 104 B Wang (ref27) 2022; 13 H Abboud (ref1) 2021; 92 L Bataller (ref33) 2007; 78 J J Gagnier (ref10) 2013; 7 A K Datta (ref15) 2021; 24 Y Zhang (ref29) 2020; 99 D Dubey (ref2) 2018; 83 E Sechi (ref22) 2021; 12 R Waitzberg (ref38) 2021; 99 G T Pagaling (ref7) 2022; 13 J Broadley (ref16) 2019; 96 J I Byun (ref36) 2015; 193 J Dalmau (ref21) 2004; 127 B Joubert (ref30) 2020; 267 C Steriade (ref23) 2020; 61 I C Bygbjerg (ref8) 2012; 337 J-I Byun (ref28) 2016; 11 C Ball (ref13) 2022; 84 G A Vasconcelos (ref20) 2021; 11 X Liu (ref25) 2017; 58 P Turcano (ref4) 2022; 35 M J Titulaer (ref11) 2013; 81 J Schubert (ref26) 2018; 6 X Xu (ref12) 2019; 7 F Graus (ref5) 2016; 15 B von Rhein (ref32) 2017; 135 A D DeSena (ref37) 2015; 30 J Morena (ref18) 2021; 11 Gagnier, JJ; Kienle, G; Altman, DG; Moher, D; Sox, H; Riley, D 2013; 7 Zhang, Y; Deng, C; Zhu, L; Ling, L 2020; 99 Dade, M; Berzero, G; Izquierdo, C 2020; 21 Ball, C; Fisicaro, R; Morris III, L 2022; 84 Chi, X; Zhou, D 2017; 136 Dalmau, J; Graus, F; Villarejo, A 2004; 127 von Rhein, B; Wagner, J; Widman, G; Malter, MP; Elger, CE; Helmstaedter, C 2017; 135 Turcano, P; Day, GS 2022; 35 Datta, AK; Pandit, A; Biswas, S; Biswas, A; Roy, BK; Gangopaddhyay, G 2021; 24 Abboud, H; Probasco, JC; Irani, S 2021; 92 Pagaling, GT; Turalde, CWR; Jamora, RDG 2022; 13 Herard, K; Khanni, JL; Alusma-Hibbert, K; Samuels, CR; Espinosa, PS 2019; 11 Vasconcelos, GA; Barreira, RM; Antoniollo, KENT 2021; 11 Liu, X; Yan, B; Wang, R 2017; 58 Graus, F; Titulaer, MJ; Balu, R 2016; 15 Dubey, D; Pittock, SJ; Kelly, CR 2018; 83 Byun, JI; Lee, ST; Moon, J 2015; 193 Byun, J-I; Lee, S-T; Jung, K-H 2016; 11 Ruiz-García, R; Muñoz-Sánchez, G; Naranjo, L 2021; 12 Bygbjerg, IC 2012; 337 Wang, B; Wang, C; Feng, J; Hao, M; Guo, S 2022; 13 Sechi, E; Flanagan, EP 2021; 12 Titulaer, MJ; McCracken, L; Gabilondo, I 2013; 81 Steriade, C; Britton, J; Dale, RC 2020; 61 DeSena, AD; Noland, DK; Matevosyan, K 2015; 30 Joubert, B; Belbezier, A; Haesebaert, J 2020; 267 Morena, J; Elsheikh, B; Hoyle, JC 2021; 11 Broadley, J; Seneviratne, U; Beech, P 2019; 96 Falip, M; Jaraba, S; Rodríguez-Bel, L 2020; 81 Endres, D; Lüngen, E; Hasan, A 2022; 27 Wingfield, T; McHugh, C; Vas, A 2011; 104 Dalmau, J; Gleichman, AJ; Hughes, EG 2008; 7 Waitzberg, R; Quentin, W; Webb, E; Glied, S 2021; 99 Zhang, W; Wang, X; Shao, N; Ma, R; Meng, H 2019; 94 Schubert, J; Brämer, D; Huttner, HB 2018; 6 Bataller, L; Kleopa, KA; Wu, GF; Rossi, JE; Rosenfeld, MR; Dalmau, J 2007; 78 Aurangzeb, S; Symmonds, M; Knight, RK; Kennett, R; Wehner, T; Irani, SR 2017; 50 Xu, X; Lu, Q; Huang, Y 2019; 7 |
References_xml | – volume: 84 start-page: 1 year: 2022 ident: ref13 article-title: Brain on fire: an imaging-based review of autoimmune encephalitis publication-title: Clin Imaging doi: 10.1016/j.clinimag.2021.12.011 – volume: 136 start-page: 738 issue: 06 year: 2017 ident: ref14 article-title: Risk factors for mortality in patients with anti-NMDA receptor encephalitis: Reply to comment on data sparsity publication-title: Acta Neurol Scand doi: 10.1111/ane.12791 – volume: 24 start-page: 383 issue: 03 year: 2021 ident: ref15 article-title: Spectrum of Anti-NMDA Receptor Antibody Encephalitis: Clinical Profile, Management and Outcomes publication-title: Ann Indian Acad Neurol doi: 10.4103/aian.AIAN_817_20 – volume: 99 start-page: e19601 issue: 13 year: 2020 ident: ref29 article-title: Predisposing factors and prognosis of status epilepticus in patients with autoimmune encephalitis publication-title: Medicine (Baltimore) doi: 10.1097/MD.0000000000019601 – volume: 27 start-page: 1479 issue: 03 year: 2022 ident: ref3 article-title: Clinical manifestations and immunomodulatory treatment experiences in psychiatric patients with suspected autoimmune encephalitis: a case series of 91 patients from Germany publication-title: Mol Psychiatry doi: 10.1038/s41380-021-01396-4 – volume: 7 start-page: e633 issue: 01 year: 2019 ident: ref12 article-title: Anti-NMDAR encephalitis: A single-center, longitudinal study in China publication-title: Neurol Neuroimmunol Neuroinflamm doi: 10.1212/NXI.0000000000000633 – volume: 12 start-page: 691536 year: 2021 ident: ref6 article-title: Limitations of a Commercial Assay as Diagnostic Test of Autoimmune Encephalitis publication-title: Front Immunol doi: 10.3389/fimmu.2021.691536 – volume: 81 start-page: 1058 issue: 12 year: 2013 ident: ref11 article-title: Late-onset anti-NMDA receptor encephalitis publication-title: Neurology doi: 10.1212/WNL.0b013e3182a4a49c – volume: 13 start-page: 890656 year: 2022 ident: ref27 article-title: Clinical Features, Treatment, and Prognostic Factors in Neuronal Surface Antibody-Mediated Severe Autoimmune Encephalitis publication-title: Front Immunol doi: 10.3389/fimmu.2022.890656 – volume: 337 start-page: 1499 issue: 6101 year: 2012 ident: ref8 article-title: Double burden of noncommunicable and infectious diseases in developing countries publication-title: Science doi: 10.1126/science.1223466 – volume: 94 start-page: 198 year: 2019 ident: ref24 article-title: Seizure characteristics, treatment, and outcome in autoimmune synaptic encephalitis: A long-term study publication-title: Epilepsy Behav doi: 10.1016/j.yebeh.2018.10.038 – volume: 104 start-page: 921 issue: 11 year: 2011 ident: ref9 article-title: Autoimmune encephalitis: a case series and comprehensive review of the literature publication-title: QJM doi: 10.1093/qjmed/hcr111 – volume: 12 start-page: 673339 year: 2021 ident: ref22 article-title: Antibody-Mediated Autoimmune Diseases of the CNS: Challenges and Approaches to Diagnosis and Management publication-title: Front Neurol doi: 10.3389/fneur.2021.673339 – volume: 11 start-page: e0146455 issue: 01 year: 2016 ident: ref28 article-title: Effect of Immunotherapy on Seizure Outcome in Patients with Autoimmune Encephalitis: A Prospective Observational Registry Study publication-title: PLoS One doi: 10.1371/journal.pone.0146455 – volume: 92 start-page: 757 issue: 07 year: 2021 ident: ref1 article-title: Autoimmune encephalitis: proposed best practice recommendations for diagnosis and acute management publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp-2020-325300 – volume: 267 start-page: 2083 issue: 07 year: 2020 ident: ref30 article-title: Long-term outcomes in temporal lobe epilepsy with glutamate decarboxylase antibodies publication-title: J Neurol doi: 10.1007/s00415-020-09807-2 – volume: 58 start-page: 2104 issue: 12 year: 2017 ident: ref25 article-title: Seizure outcomes in patients with anti-NMDAR encephalitis: A follow-up study publication-title: Epilepsia doi: 10.1111/epi.13929 – volume: 127 start-page: 1831 year: 2004 ident: ref21 article-title: Clinical analysis of anti-Ma2-associated encephalitis publication-title: Brain doi: 10.1093/brain/awh203 – volume: 6 start-page: e514 issue: 01 year: 2018 ident: ref26 article-title: Management and prognostic markers in patients with autoimmune encephalitis requiring ICU treatment publication-title: Neurol Neuroimmunol Neuroinflamm doi: 10.1212/NXI.0000000000000514 – volume: 35 start-page: 415 issue: 03 year: 2022 ident: ref4 article-title: Life after autoantibody-mediated encephalitis: optimizing follow-up and management in recovering patients publication-title: Curr Opin Neurol doi: 10.1097/WCO.0000000000001050 – volume: 15 start-page: 391 issue: 04 year: 2016 ident: ref5 article-title: A clinical approach to diagnosis of autoimmune encephalitis publication-title: Lancet Neurol doi: 10.1016/S1474-4422(15)00401-9 – volume: 21 start-page: 3701 issue: 10 year: 2020 ident: ref19 article-title: Neurological Syndromes Associated with Anti-GAD Antibodies publication-title: Int J Mol Sci doi: 10.3390/ijms21103701 – volume: 83 start-page: 166 issue: 01 year: 2018 ident: ref2 article-title: Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis publication-title: Ann Neurol doi: 10.1002/ana.25131 – volume: 7 start-page: 223 year: 2013 ident: ref10 article-title: The CARE guidelines: consensus-based clinical case reporting guideline development publication-title: J Med Case Rep doi: 10.1186/1752-1947-7-223 – volume: 11 start-page: 263 issue: 03 year: 2021 ident: ref18 article-title: Recurrent Miller Fisher: A Case Report Along With a Literature and an EMG/NCS Review publication-title: Neurohospitalist doi: 10.1177/1941874420987053 – volume: 99 start-page: 542 issue: 02 year: 2021 ident: ref38 article-title: The Structure and Financing of Health Care Systems Affected How Providers Coped With COVID-19 publication-title: Milbank Q doi: 10.1111/1468-0009.12530 – volume: 11 start-page: e4738 issue: 05 year: 2019 ident: ref17 article-title: Neurological Disorders Associated with Glutamic Acid Decarboxylase Antibodies publication-title: Cureus – volume: 50 start-page: 14 year: 2017 ident: ref35 article-title: LGI1-antibody encephalitis is characterised by frequent, multifocal clinical and subclinical seizures publication-title: Seizure doi: 10.1016/j.seizure.2017.05.017 – volume: 30 start-page: 212 issue: 04 year: 2015 ident: ref37 article-title: Intravenous methylprednisolone versus therapeutic plasma exchange for treatment of anti-N-methyl-D-aspartate receptor antibody encephalitis: A retrospective review publication-title: J Clin Apher doi: 10.1002/jca.21363 – volume: 135 start-page: 134 issue: 01 year: 2017 ident: ref32 article-title: Suspected antibody negative autoimmune limbic encephalitis: outcome of immunotherapy publication-title: Acta Neurol Scand doi: 10.1111/ane.12575 – volume: 78 start-page: 381 issue: 04 year: 2007 ident: ref33 article-title: Autoimmune limbic encephalitis in 39 patients: immunophenotypes and outcomes publication-title: J Neurol Neurosurg Psychiatry doi: 10.1136/jnnp.2006.100644 – volume: 81 start-page: 157 year: 2020 ident: ref31 article-title: Seizures and epilepsy of autoimmune origin: A long-term prospective study publication-title: Seizure doi: 10.1016/j.seizure.2020.07.019 – volume: 193 start-page: 142 year: 2015 ident: ref36 article-title: Cardiac sympathetic dysfunction in anti-NMDA receptor encephalitis publication-title: Auton Neurosci doi: 10.1016/j.autneu.2015.08.002 – volume: 13 start-page: 788309 year: 2022 ident: ref7 article-title: Autoimmune Encephalitis in the Philippines: A Scoping Review on the Treatment Gaps, Challenges, and Current State of Care publication-title: Front Neurol doi: 10.3389/fneur.2022.788309 – volume: 61 start-page: 1341 issue: 07 year: 2020 ident: ref23 article-title: Acute symptomatic seizures secondary to autoimmune encephalitis and autoimmune-associated epilepsy: Conceptual definitions publication-title: Epilepsia doi: 10.1111/epi.16571 – volume: 7 start-page: 1091 issue: 12 year: 2008 ident: ref34 article-title: Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies publication-title: Lancet Neurol doi: 10.1016/S1474-4422(08)70224-2 – volume: 11 start-page: 606350 year: 2021 ident: ref20 article-title: Autoimmune Encephalitis in Latin America: A Critical Review publication-title: Front Neurol doi: 10.3389/fneur.2020.606350 – volume: 96 start-page: 24 year: 2019 ident: ref16 article-title: Prognosticating autoimmune encephalitis: A systematic review publication-title: J Autoimmun doi: 10.1016/j.jaut.2018.10.014 – volume: 27 start-page: 1479 issue: 03 year: 2022 end-page: 1489 article-title: Clinical manifestations and immunomodulatory treatment experiences in psychiatric patients with suspected autoimmune encephalitis: a case series of 91 patients from Germany publication-title: Mol Psychiatry – volume: 7 start-page: 223 year: 2013 end-page: 223 article-title: The CARE guidelines: consensus-based clinical case reporting guideline development publication-title: J Med Case Rep – volume: 11 issue: 05 year: 2019 article-title: Neurological Disorders Associated with Glutamic Acid Decarboxylase Antibodies publication-title: Cureus – volume: 337 start-page: 1499 issue: 6101 year: 2012 end-page: 1501 article-title: Double burden of noncommunicable and infectious diseases in developing countries publication-title: Science – volume: 81 start-page: 1058 issue: 12 year: 2013 end-page: 1063 article-title: Late-onset anti-NMDA receptor encephalitis publication-title: Neurology – volume: 12 start-page: 673339 year: 2021 end-page: 673339 article-title: Antibody-Mediated Autoimmune Diseases of the CNS: Challenges and Approaches to Diagnosis and Management publication-title: Front Neurol – volume: 136 start-page: 738 issue: 06 year: 2017 end-page: 738 article-title: Risk factors for mortality in patients with anti-NMDA receptor encephalitis: Reply to comment on data sparsity publication-title: Acta Neurol Scand – volume: 83 start-page: 166 issue: 01 year: 2018 end-page: 177 article-title: Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis publication-title: Ann Neurol – volume: 135 start-page: 134 issue: 01 year: 2017 end-page: 141 article-title: Suspected antibody negative autoimmune limbic encephalitis: outcome of immunotherapy publication-title: Acta Neurol Scand – volume: 267 start-page: 2083 issue: 07 year: 2020 end-page: 2089 article-title: Long-term outcomes in temporal lobe epilepsy with glutamate decarboxylase antibodies publication-title: J Neurol – volume: 81 start-page: 157 year: 2020 end-page: 165 article-title: Seizures and epilepsy of autoimmune origin: A long-term prospective study publication-title: Seizure – volume: 50 start-page: 14 year: 2017 end-page: 17 article-title: LGI1-antibody encephalitis is characterised by frequent, multifocal clinical and subclinical seizures publication-title: Seizure – volume: 7 start-page: 1091 issue: 12 year: 2008 end-page: 1098 article-title: Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies publication-title: Lancet Neurol – volume: 96 start-page: 24 year: 2019 end-page: 34 article-title: Prognosticating autoimmune encephalitis: A systematic review publication-title: J Autoimmun – volume: 84 start-page: 1 year: 2022 end-page: 30 article-title: Brain on fire: an imaging-based review of autoimmune encephalitis publication-title: Clin Imaging – volume: 11 start-page: 606350 year: 2021 end-page: 606350 article-title: Autoimmune Encephalitis in Latin America: A Critical Review publication-title: Front Neurol – volume: 94 start-page: 198 year: 2019 end-page: 203 article-title: Seizure characteristics, treatment, and outcome in autoimmune synaptic encephalitis: A long-term study publication-title: Epilepsy Behav – volume: 127 start-page: 1831 issue: Pt 8 year: 2004 end-page: 1844 article-title: Clinical analysis of anti-Ma2-associated encephalitis publication-title: Brain – volume: 11 issue: 01 year: 2016 article-title: Effect of Immunotherapy on Seizure Outcome in Patients with Autoimmune Encephalitis: A Prospective Observational Registry Study publication-title: PLoS One – volume: 35 start-page: 415 issue: 03 year: 2022 end-page: 422 article-title: Life after autoantibody-mediated encephalitis: optimizing follow-up and management in recovering patients publication-title: Curr Opin Neurol – volume: 58 start-page: 2104 issue: 12 year: 2017 end-page: 2111 article-title: Seizure outcomes in patients with anti-NMDAR encephalitis: A follow-up study publication-title: Epilepsia – volume: 193 start-page: 142 year: 2015 end-page: 146 article-title: Cardiac sympathetic dysfunction in anti-NMDA receptor encephalitis publication-title: Auton Neurosci – volume: 104 start-page: 921 issue: 11 year: 2011 end-page: 931 article-title: Autoimmune encephalitis: a case series and comprehensive review of the literature publication-title: QJM – volume: 24 start-page: 383 issue: 03 year: 2021 end-page: 389 article-title: Spectrum of Anti-NMDA Receptor Antibody Encephalitis: Clinical Profile, Management and Outcomes publication-title: Ann Indian Acad Neurol – volume: 6 issue: 01 year: 2018 article-title: GENERATE and IGNITE network. Management and prognostic markers in patients with autoimmune encephalitis requiring ICU treatment publication-title: Neurol Neuroimmunol Neuroinflamm – volume: 78 start-page: 381 issue: 04 year: 2007 end-page: 385 article-title: Autoimmune limbic encephalitis in 39 patients: immunophenotypes and outcomes publication-title: J Neurol Neurosurg Psychiatry – volume: 21 start-page: 3701 issue: 10 year: 2020 end-page: 3701 article-title: Neurological Syndromes Associated with Anti-GAD Antibodies publication-title: Int J Mol Sci – volume: 61 start-page: 1341 issue: 07 year: 2020 end-page: 1351 article-title: Acute symptomatic seizures secondary to autoimmune encephalitis and autoimmune-associated epilepsy: Conceptual definitions publication-title: Epilepsia – volume: 13 start-page: 788309 year: 2022 end-page: 788309 article-title: Autoimmune Encephalitis in the Philippines: A Scoping Review on the Treatment Gaps, Challenges, and Current State of Care publication-title: Front Neurol – volume: 92 start-page: 757 issue: 07 year: 2021 end-page: 768 article-title: Autoimmune Encephalitis Alliance Clinicians Network. Autoimmune encephalitis: proposed best practice recommendations for diagnosis and acute management publication-title: J Neurol Neurosurg Psychiatry – volume: 99 issue: 13 year: 2020 article-title: Predisposing factors and prognosis of status epilepticus in patients with autoimmune encephalitis publication-title: Medicine (Baltimore) – volume: 13 start-page: 890656 year: 2022 end-page: 890656 article-title: Clinical Features, Treatment, and Prognostic Factors in Neuronal Surface Antibody-Mediated Severe Autoimmune Encephalitis publication-title: Front Immunol – volume: 12 start-page: 691536 year: 2021 end-page: 691536 article-title: Limitations of a Commercial Assay as Diagnostic Test of Autoimmune Encephalitis publication-title: Front Immunol – volume: 30 start-page: 212 issue: 04 year: 2015 end-page: 216 article-title: Intravenous methylprednisolone versus therapeutic plasma exchange for treatment of anti-N-methyl-D-aspartate receptor antibody encephalitis: A retrospective review publication-title: J Clin Apher – volume: 11 start-page: 263 issue: 03 year: 2021 end-page: 266 article-title: Recurrent Miller Fisher: A Case Report Along With a Literature and an EMG/NCS Review publication-title: Neurohospitalist – volume: 7 issue: 01 year: 2019 article-title: Anti-NMDAR encephalitis: A single-center, longitudinal study in China publication-title: Neurol Neuroimmunol Neuroinflamm – volume: 99 start-page: 542 issue: 02 year: 2021 end-page: 564 article-title: The Structure and Financing of Health Care Systems Affected How Providers Coped With COVID-19 publication-title: Milbank Q – volume: 15 start-page: 391 issue: 04 year: 2016 end-page: 404 article-title: A clinical approach to diagnosis of autoimmune encephalitis publication-title: Lancet Neurol |
SSID | ssj0024997 |
Score | 2.363568 |
Snippet | Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present... Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present at the... Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present... Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be present... Abstract Background Autoimmune encephalitis (AE) consists of a group of acquired diseases that affect the central nervous system. A myriad of phenotypes may be... |
SourceID | doaj scielo pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 1 |
SubjectTerms | Autoantibodies Autoanticorpos Autoimmune diseases Central nervous system Cerebrospinal fluid Convulsões Diagnosis EEG Electronic medical records Encefalite Límbica Encephalitis Epilepsy Limbic Encephalitis Mortality Neuroimaging Neurological complications NEUROSCIENCES Original Paraneoplastic Syndromes, Nervous System Patients Phenotypes PSYCHIATRY Public health Seizures Síndromes Paraneoplásicas do Sistema Nervoso |
Title | Autoimmune encephalitis in a resource-limited public health setting: a case series analysis |
URI | https://www.ncbi.nlm.nih.gov/pubmed/38325385 https://www.proquest.com/docview/3032620119 https://www.proquest.com/docview/2923914037 https://pubmed.ncbi.nlm.nih.gov/PMC10849825 http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2024000200201&lng=en&tlng=en https://doaj.org/article/1b26c8a37a224834b0386d2d17f5dbad |
Volume | 82 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVAFT databaseName: Open Access Digital Library customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: KQ8 dateStart: 19980101 isFulltext: true titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html providerName: Colorado Alliance of Research Libraries – providerCode: PRVAFT databaseName: Open Access Digital Library customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: KQ8 dateStart: 19430601 isFulltext: true titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html providerName: Colorado Alliance of Research Libraries – providerCode: PRVAON databaseName: DOAJ Directory of Open Access Journals customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: DOA dateStart: 20000101 isFulltext: true titleUrlDefault: https://www.doaj.org/ providerName: Directory of Open Access Journals – providerCode: PRVBFR databaseName: Free Medical Journals customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: DIK dateStart: 19430101 isFulltext: true titleUrlDefault: http://www.freemedicaljournals.com providerName: Flying Publisher – providerCode: PRVFQY databaseName: GFMER Free Medical Journals customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: GX1 dateStart: 0 isFulltext: true titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php providerName: Geneva Foundation for Medical Education and Research – providerCode: PRVAQN databaseName: PubMed Central customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: RPM dateStart: 20210101 isFulltext: true titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/ providerName: National Library of Medicine – providerCode: PRVAWY databaseName: Thieme Connect Journals Open Access customDbUrl: eissn: 1678-4227 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0024997 issn: 0004-282X databaseCode: 0U6 dateStart: 20220101 isFulltext: true titleUrlDefault: http://open.thieme.com providerName: Thieme |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYllNJL6btu0qBCoScR62VLuaWlIRTSSxtY6EF4ZJksLN4Q7_7_zFj2Nktbein4JA1mGH3yzHg0nxj7UJWpMTJ2AnPlSpjWa-Ft54ShtkyoJGhFvcOX36qLK_N1YRf3rvqiM2GZHjgb7kSCqqJrdN2gs3HaQKld1apW1p1toWnp64tubE6mZpY97zNbZmkEJhWLma7R2pNBUBFTSCLas2bPHY2s_X8KNX8_MfmQHNTqvi86f8qeTEEkP8vKP2MPUv-cPbqcyuQv2M-z7Wa9pM6PxGnn3lxTtL0c-LLnDb-d_tiLVW5u4pnqmueWSD6k8Sj0KUpGdHGcMJoG3kzsJS_Z1fmXH58vxHSLgogY22xE3boWPCgXuyYCZn9RQ-Urb9CeurKACyUdgFKgSm3r2hExAc6XCQCTEdCv2EG_7tMbxpOMEFXb6OiisdG70nSxBIx8jU04XjAxGzPEiWKcbrpYhbHUbW0YAhk_TMYv2Med_E0m1_ir5Cdam50UkWKPAwiVMEEl_AsqBTuaVzZMO3UI6MKJk19KX7D3u2ncY1Q4afq03g5BYRTsidiwLtjrDISdJpjhK3QatmBuDyJ7qu7P9Mvrkcdbls54zNDRDBlNv7T6TsgNhFxFJHQU1OMj3_4PMxyyx_TSfPT8iB1sbrfpHUZWGzgeN9Hx-MvrDrwqHSk |
linkProvider | Directory of Open Access Journals |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Autoimmune+encephalitis+in+a+resource-limited+public+health+setting%3A+a+case+series+analysis&rft.jtitle=Arquivos+de+neuro-psiquiatria&rft.au=Morillos%2C+Matheus+Bernardon&rft.au=Borelli%2C+Wyllians+Vendramini&rft.au=Noll%2C+Giovani&rft.au=Piccini%2C+Cristian+Daniel&rft.date=2024-02-01&rft.issn=1678-4227&rft.eissn=1678-4227&rft.volume=82&rft.issue=2&rft.spage=1&rft_id=info:doi/10.1055%2Fs-0044-1779054&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0004-282X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0004-282X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0004-282X&client=summon |