Comorbidities in multiple sclerosis—a plea for interdisciplinary collaboration to improve the quality of life of MS patients

The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achievi...

Full description

Saved in:
Bibliographic Details
Published inDegenerative neurological and neuromuscular disease Vol. 9; pp. 39 - 53
Main Author Goischke, Hans-Klaus
Format Journal Article
LanguageEnglish
Published New Zealand Dove Medical Press Limited 01.06.2019
Dove
Subjects
Online AccessGet full text
ISSN1179-9900
1179-9900
DOI10.2147/DNND.S204555

Cover

Abstract The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase ( ). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a "multipurpose steroid hormone", it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD add-on therapy being almost unproblematic and most likely to be accepted by PwMS.
AbstractList The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase (CYP24A1). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) CYP24A1 gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a "multipurpose steroid hormone", it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD add-on therapy being almost unproblematic and most likely to be accepted by PwMS.The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase (CYP24A1). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) CYP24A1 gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a "multipurpose steroid hormone", it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD add-on therapy being almost unproblematic and most likely to be accepted by PwMS.
The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase ( ). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a "multipurpose steroid hormone", it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD add-on therapy being almost unproblematic and most likely to be accepted by PwMS.
The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase (CYP24A1). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) CYP24A1 gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a “multipurpose steroid hormone”, it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD add-on therapy being almost unproblematic and most likely to be accepted by PwMS.
The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase (CYP24A1). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) CYP24A1 gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a "multipurpose steroid hormone", it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD addon therapy being almost unproblematic and most likely to be accepted by PwMS. Keywords: comorbidities in multiple sclerosis, improving quality of life, vitamin D therapy, pregnancy in MS
The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by numerous international studies in long-term care. One therapeutic option would be an add-on therapy with vitamin D (VD), with the aim of achieving a therapeutically effective dose. The individually required VD dose must be tested, since the response to a certain dose is subject to variations between individuals. A possible toxicity with increased 1.25(OH)D3 (active VD metabolite) is largely prevented by increased activity of 24-hydroxylase (CYP24A1). Monitoring of serum VD levels as well as serum calcium and phosphate levels (optional Ca excretion in 24-hour urine, Ca creatinine ratio in urine) provides safety and is necessary because possible mutations on the (catabolic) CYP24A1 gene can lead to a partial or total loss of 24-hydroxylase activity and provoke hypercalcemia/hyperphosphatemia. The main therapeutic objective is to maintain functional and social independence by using drugs with a high safety profile. The prevention and optimal management of comorbidities can influence the quality of life of patients with MS (PwMS) when included in patient care. Adequate measures can reduce the burden of MS only if the risk of comorbidity is reduced through targeted monitoring, early detection and diagnosis. Such a strategy will contribute to influencing the premature mortality of patients with MS. If VD is recognized as a "multipurpose steroid hormone", it could also be used to maintain cognitive function and prevent premature possible dementia, especially as there is evidence that VD deficiency correlates with brain atrophy (hippocampus). At present, MS therapy is still a balancing act between therapeutically efficient action and the management of unexpected side effects, with VD addon therapy being almost unproblematic and most likely to be accepted by PwMS.
Audience Academic
Author Goischke, Hans-Klaus
Author_xml – sequence: 1
  givenname: Hans-Klaus
  surname: Goischke
  fullname: Goischke, Hans-Klaus
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31354380$$D View this record in MEDLINE/PubMed
BookMark eNptks1u1DAQxyNUREvpjTOyhIQ4kMWxk41zqVRt-ZJKOSycLccZd40cO7Wdor1UfQiekCfBYcuyW2Efxhr_ZjTzn3maHVhnIcueF3hGirJ-e355eT5bElxWVfUoOyqKusmbBuODnfdhdhLCd5xOxYqG1k-yQ1rQqqQMH2W3C9c73-pORw0BaYv60UQ9GEBBGvAu6PDr7qdAySOQcj4hEXyng0yQtsKvkXTGiNZ5EbWzKDqk-8G7G0BxBeh6FEbHNXIKGa1gsp-XaEgs2BieZY-VMAFO7u1x9u39u6-Lj_nFlw-fFmcXuSwLEvNStnNohcStZKwuJQYqFQHadlVTJYIRJTBpO1bTCiiuSAOskEQpQplUDOhxlm_yjnYQ6x_CGD543afqeYH5JCXvrO142EiZ-NMNP4xtD51MtXrxL8YJzfd_rF7xK3fD5xUrCZsSvL5P4N31CCHyPkkGSSgLbgyckPmclqysy4S-3KBXwgDXVrmUUU44P5vjBBBCmkTN_kOl20GvZdoKpZN_L-DVTsAKhImr4Mw4DSnsgy92e902-XdJEkA2gEzrEDwoLnX8M-xUgjZbBadl5Mutgm8eBD0UfA__Dfbr4Vg
CitedBy_id crossref_primary_10_1515_nipt_2024_0007
crossref_primary_10_20538_1682_0363_2024_1_116_125
crossref_primary_10_1186_s12889_024_20056_0
crossref_primary_10_1093_arclin_acad097
crossref_primary_10_1093_arclin_acac025
ContentType Journal Article
Copyright COPYRIGHT 2019 Dove Medical Press Limited
2019 Goischke. 2019 Goischke.
Copyright_xml – notice: COPYRIGHT 2019 Dove Medical Press Limited
– notice: 2019 Goischke. 2019 Goischke.
DBID AAYXX
CITATION
NPM
7X8
5PM
ADTOC
UNPAY
DOI 10.2147/DNND.S204555
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
Unpaywall for CDI: Periodical Content
Unpaywall
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
PubMed




Database_xml – sequence: 1
  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
– sequence: 2
  dbid: UNPAY
  name: Unpaywall
  url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/
  sourceTypes: Open Access Repository
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
DocumentTitleAlternate Goischke
EISSN 1179-9900
EndPage 53
ExternalDocumentID 10.2147/dnnd.s204555
PMC6584285
A607432229
31354380
10_2147_DNND_S204555
Genre Journal Article
GeographicLocations Germany
GeographicLocations_xml – name: Germany
GroupedDBID 0YH
5VS
8FI
8FJ
8G5
AAYXX
ABUWG
ADBBV
AFKRA
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BENPR
BPHCQ
BVXVI
CCPQU
CITATION
DWQXO
FYUFA
GNUQQ
GUQSH
HYE
IAO
IHR
IHW
ITC
KQ8
M2M
M2O
OK1
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSYQQ
PUEGO
RPM
TDBHL
TUS
UKHRP
VDV
ALIPV
GROUPED_DOAJ
M~E
NPM
PMFND
7X8
5PM
ADTOC
UNPAY
ID FETCH-LOGICAL-c412t-4cb6ebac0bc8874c0e3cf2e3bd59541282fa02bd8735e30529e81c2ff238cf8e3
IEDL.DBID UNPAY
ISSN 1179-9900
IngestDate Wed Oct 01 15:46:37 EDT 2025
Tue Sep 30 16:43:10 EDT 2025
Fri Sep 05 12:01:52 EDT 2025
Tue Jun 17 21:30:20 EDT 2025
Tue Jun 10 20:19:24 EDT 2025
Thu May 22 21:05:39 EDT 2025
Thu Jan 02 22:31:35 EST 2025
Thu Apr 24 23:11:48 EDT 2025
Wed Oct 01 02:02:03 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords comorbidities in multiple sclerosis
improving quality of life
vitamin D therapy
pregnancy in MS
Language English
License http://creativecommons.org/licenses/by-nc/3.0
This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
cc-by-nc
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c412t-4cb6ebac0bc8874c0e3cf2e3bd59541282fa02bd8735e30529e81c2ff238cf8e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://proxy.k.utb.cz/login?url=https://www.dovepress.com/getfile.php?fileID=50514
PMID 31354380
PQID 2266348474
PQPubID 23479
PageCount 15
ParticipantIDs unpaywall_primary_10_2147_dnnd_s204555
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6584285
proquest_miscellaneous_2266348474
gale_infotracmisc_A607432229
gale_infotracacademiconefile_A607432229
gale_healthsolutions_A607432229
pubmed_primary_31354380
crossref_citationtrail_10_2147_DNND_S204555
crossref_primary_10_2147_DNND_S204555
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20190601
PublicationDateYYYYMMDD 2019-06-01
PublicationDate_xml – month: 06
  year: 2019
  text: 20190601
  day: 01
PublicationDecade 2010
PublicationPlace New Zealand
PublicationPlace_xml – name: New Zealand
PublicationTitle Degenerative neurological and neuromuscular disease
PublicationTitleAlternate Degener Neurol Neuromuscul Dis
PublicationYear 2019
Publisher Dove Medical Press Limited
Dove
Publisher_xml – name: Dove Medical Press Limited
– name: Dove
SSID ssj0000581937
Score 2.1234627
Snippet The negative influence of comorbidities on the quality of life of people with multiple sclerosis is evident and the problem is increasingly acknowledged by...
SourceID unpaywall
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 39
SubjectTerms Brain
Comorbidity
Cytochrome P-450
Dementia
Genes
Health aspects
Hormones
Long term care
Metabolites
Mortality
Multiple sclerosis
Phosphates
Prevention
Review
Toxicity
Vitamin D
Vitamins
Title Comorbidities in multiple sclerosis—a plea for interdisciplinary collaboration to improve the quality of life of MS patients
URI https://www.ncbi.nlm.nih.gov/pubmed/31354380
https://www.proquest.com/docview/2266348474
https://pubmed.ncbi.nlm.nih.gov/PMC6584285
https://www.dovepress.com/getfile.php?fileID=50514
UnpaywallVersion publishedVersion
Volume 9
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 1179-9900
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000581937
  issn: 1179-9900
  databaseCode: KQ8
  dateStart: 20110101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAQN
  databaseName: PubMed Central
  customDbUrl:
  eissn: 1179-9900
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000581937
  issn: 1179-9900
  databaseCode: RPM
  dateStart: 20120101
  isFulltext: true
  titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/
  providerName: National Library of Medicine
– providerCode: PRVPQU
  databaseName: ProQuest Central
  customDbUrl: http://www.proquest.com/pqcentral?accountid=15518
  eissn: 1179-9900
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000581937
  issn: 1179-9900
  databaseCode: BENPR
  dateStart: 20110101
  isFulltext: true
  titleUrlDefault: https://www.proquest.com/central
  providerName: ProQuest
– providerCode: PRVAWR
  databaseName: Taylor & Francis Open Access
  customDbUrl:
  eissn: 1179-9900
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000581937
  issn: 1179-9900
  databaseCode: 0YH
  dateStart: 20111201
  isFulltext: true
  titleUrlDefault: https://www.tandfonline.com
  providerName: Taylor & Francis
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3bbtNAEB21iQS8cL8ESlgkLg-Vi-NdO-vHQFtFSI0qSqT2yVqv18IisqvYAZUHxEfwhXwJM17HioOQ4ClRdqJ4MzO7x94zZwBepGJsYhUqR4aB7wiVuI5UkjvKJGMtjRZpXLMtZsF0Lt6f--c74K1rYYhWmRRfLAvUPk0yFUkU1WIR9IZ41CTavQv9gA6VetCfz04nF7aLSujg8upahju14HmT5DmuQyS6TtV8G3vP9gq8sQVt0yOvr_JLdfVVLRYbe8_xLVsPWNaShUQ5-XywquID_W1L0PH_pnUbbjZQlE1s7NyBHZPfhWsnzWH7PfiOa0WxjLOkFl1lWc7W7ENW4hdwiln568dPxfATxRD8MtKeWG7W-bJOmLGqYFn9EMMwxJ3MFnResSJliyw19Hpyxhql1_I-zI-PPr6bOk27BkeLkVc5QscB-l27scaVS2jXcJ16hseJH_poIb1UuV6cyDH3DacTRiNH2ktTRA06lYY_gF5e5OYRMG1C7SYjGctECF_7MlTcjLTkgUG4J_gA9teOjHSjZU4tNRYR3tOQ26PD2ewwOrNuH8DL1vrSanj8xe4ZxURkK1Db1I8mAeEsanw-gNe1BSU__p5WTQ0DXjX5sGO517HEpNWd4efruItoiJhuuSlWZYRwOOACMYMYwEMbh-1F8xH3qUPAAMadCG0NSCu8O5Jnn2rNcAKansQpvmpj-Y__glIlalLl8b8aPoEbiCFDy57bg161XJmniNOqeAi77sV0CP23R7PTD8MmTX8DsjlG8Q
linkProvider Unpaywall
linkToUnpaywall http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3fi9NAEB7OHqgv_vasnrqCPx4kd0l2k24ei-dxCFeEs3A-hd3NBoMlOZpUOR_EP8K_0L_EmWwamoqgTy3dKc12Zna_ZL_5BuB5LiZWq0R5MokjT6jM96SS3FM2mxhpjch1y7aYxSdz8e48Ot-BcF0LQ7TKrPriWKDuaZJtSKKoFYugN8SjJtHuK7Ab06HSCHbns_fTj66LSuLh8uo7hju14DnMyhLXIRJdp2q-jb1newXe2IK26ZHXVuWFuvyqFouNvef4pqsHrFvJQqKcfD5YNfrAfNsSdPy_ad2CGx0UZVMXO7dhx5Z34Oppd9h-F77jWlEtdZG1oqusKNmafchq_AJOsah__fipGH6iGIJfRtoTy806XzYIM9ZUrGgfYliGuJO5gs5LVuVsUeSWXk_PWKf0Wt-D-fHbD29OvK5dg2dEEDaeMDpGvxtfG1y5hPEtN3louc6iJEILGebKD3UmJzyynE4YrQxMmOeIGkwuLb8Po7Iq7QNgxibGzwKpZSZEZCKZKG4DI3lsEe4JPobXa0emptMyp5YaixTvacjt6dFsdpSeObeP4UVvfeE0PP5i95RiInUVqH3qp9OYcBY1Ph_Dq9aCkh9_z6iuhgGvmnw4sNwfWGLSmsHws3XcpTRETLfSVqs6RTgcc4GYQYxhz8Vhf9E84BF1CBjDZBChvQFphQ9HyuJTqxlOQDOUOMWXfSz_8V9QqqRdqjz8V8NHcB0xZOLYc_swapYr-xhxWqOfdIn5G-iVRGU
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=Comorbidities+in+multiple+sclerosis-a+plea+for+interdisciplinary+collaboration+to+improve+the+quality+of+life+of+MS+patients&rft.jtitle=Degenerative+neurological+and+neuromuscular+disease&rft.au=Goischke%2C+Hans-Klaus&rft.date=2019-06-01&rft.eissn=1179-9900&rft.volume=9&rft.spage=39&rft_id=info:doi/10.2147%2FDNND.S204555&rft_id=info%3Apmid%2F31354380&rft.externalDocID=31354380
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1179-9900&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1179-9900&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1179-9900&client=summon