Adult-onset cerebello-brainstem-dominant form of X-linked adrenoleukodystrophy with auditory pathway involvement: A case report
X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms and imaging findings can mimic spinocerebellar degeneration (SCD), making diagnosis difficult. Herein, we report a case that we initially di...
Saved in:
| Published in | Tenri Medical Bulletin Vol. 27; no. 1; pp. 33 - 39 |
|---|---|
| Main Authors | , , , , , , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Tenri Foundation, Tenri Institute of Medical Research
25.12.2024
|
| Subjects | |
| Online Access | Get full text |
| ISSN | 1344-1817 2187-2244 2187-2244 |
| DOI | 10.12936/tenrikiyo.27-009 |
Cover
| Abstract | X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms and imaging findings can mimic spinocerebellar degeneration (SCD), making diagnosis difficult. Herein, we report a case that we initially diagnosed as SCD but was eventually diagnosed as the cerebello-brainstem-dominant form of X-ALD. The patient presented with psychiatric symptoms in adulthood. He subsequently developed gait disturbance and was referred to the neurology department of our hospital. Initial magnetic resonance imaging (MRI) showed atrophy of the cerebellum and pons, and abnormal signals in various regions, including the middle cerebellar peduncles, the corpus callosum, infero-posterior part of the bilateral thalami, and lateral edges of the midbrain, on T2-weighted imaging. The patient was followed up as SCD; however, his symptoms and MRI findings worsened. Further examination was performed, and the diagnosis of X-ALD was made. Abnormal signals in the thalami and midbrain on MRI are considered to correspond to the medial geniculate bodies and the brachia of the inferior colliculus, respectively. They constitute the auditory pathway, which is an evaluation item in Loes score, an imaging-based scoring system for patients with X-ALD. Recognizing abnormalities in the bilateral auditory pathway may aid accurate diagnosis of X-ALD. |
|---|---|
| AbstractList | X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms and imaging findings can mimic spinocerebellar degeneration (SCD), making diagnosis difficult. Herein, we report a case that we initially diagnosed as SCD but was eventually diagnosed as the cerebello-brainstem-dominant form of X-ALD. The patient presented with psychiatric symptoms in adulthood. He subsequently developed gait disturbance and was referred to the neurology department of our hospital. Initial magnetic resonance imaging (MRI) showed atrophy of the cerebellum and pons, and abnormal signals in various regions, including the middle cerebellar peduncles, the corpus callosum, infero-posterior part of the bilateral thalami, and lateral edges of the midbrain, on T2-weighted imaging. The patient was followed up as SCD; however, his symptoms and MRI findings worsened. Further examination was performed, and the diagnosis of X-ALD was made. Abnormal signals in the thalami and midbrain on MRI are considered to correspond to the medial geniculate bodies and the brachia of the inferior colliculus, respectively. They constitute the auditory pathway, which is an evaluation item in Loes score, an imaging-based scoring system for patients with X-ALD. Recognizing abnormalities in the bilateral auditory pathway may aid accurate diagnosis of X-ALD. |
| ArticleNumber | 27-009 |
| Author | Yasumura, Sumika Shinde, Akiyo Kim, Hyunjin Imaeda, Masaki Kanao, Shotaro Kubo, Takeshi Yasuo, Shunsuke Yuge, Shunsuke Taniguchi, Takanori Okubo, Gosuke Ota, Rie Noma, Satoshi Suzuki, Mizue Nakamura, Yuri Yokota, Yusuke Noda, Toshiyuki Minami, Akihiko Yamashita, Naoki Saito, Ayako Suenaga, Toshihiko Kawase, Kango |
| Author_xml | – sequence: 1 fullname: Yokota, Yusuke organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Minami, Akihiko organization: Department of Radiology, Kyoto City Hospital – sequence: 1 fullname: Kawase, Kango organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Taniguchi, Takanori organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Okubo, Gosuke organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Shinde, Akiyo organization: Department of Neurology, Tenri Hospital – sequence: 1 fullname: Kanao, Shotaro organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Kubo, Takeshi organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Suenaga, Toshihiko organization: Department of Neurology, Tenri Hospital – sequence: 1 fullname: Yasumura, Sumika organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Suzuki, Mizue organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Ota, Rie organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Yuge, Shunsuke organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Noma, Satoshi organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Yamashita, Naoki organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Saito, Ayako organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Kim, Hyunjin organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Noda, Toshiyuki organization: Department of Radiology, Kobe City Medical Center General Hospital – sequence: 1 fullname: Nakamura, Yuri organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Yasuo, Shunsuke organization: Department of Radiology, Tenri Hospital – sequence: 1 fullname: Imaeda, Masaki organization: Department of Radiology, Tenri Hospital |
| BookMark | eNqN0MFuEzEQBmALFYlQ-gDc_AIuY-9u7OUWVRSQKnEpErfVxJ4lbrz2ynYa7YlXbyAoEjcuM5f5fmn-t-wqpkiMvZdwK1XfrD9Uitnv_ZJulRYA_Su2UtJooVTbXrGVbNpWSCP1G3ZTyhMANA2sQZkV-7Vxh1BFioUqt5RpSyEksc3oY6k0CZcmHzFWPqY88TTyHyL4uCfH0WWKKdBhn9xSak7zbuFHX3ccD87XlBc-Y90dceE-PqfwTBPF-pFvuMVCPNOccn3HXo8YCt383dfs-_2nx7sv4uHb5693mwdhpVa9QBqdWZNRtiGQpnMWsDMOVNe0sNUwagldb3S_7YB6rRBP31lQ4xo7bWBsrpk65x7ijMsRQxjm7CfMyyBh-NPicGlxUHo4tXhC8oxsTqVkGv_L3J_NU6n4ky4Cc_U20L9A_h5neDmwO8wDxeYFTFqYCg |
| Cites_doi | 10.1212/WNL.31.10.1241 10.1186/1750-1172-7-51 10.1148/rg.253045118 10.1111/j.1365-2990.2007.00933.x 10.1016/j.parkreldis.2020.01.018 10.1016/S0303-8467(99)00028-1 10.1007/s00415-021-10915-w 10.2463/mrms.3.133 10.2214/ajr.179.1.1790251 10.1007/s13244-016-0490-9 10.1038/361726a0 10.3390/tomography8010035 10.1186/s13317-019-0117-5 10.1212/01.WNL.0000079050.91337.83 10.1371/journal.pone.0177296 10.1371/journal.pone.0022766 10.1016/0014-5793(94)00400-5 10.2214/AJR.13.11400 10.3389/fneur.2022.999419 10.1007/s100380200090 10.2214/AJR.11.8080 10.1111/neup.12230 |
| ContentType | Journal Article |
| Copyright | Tenri Foundation, Tenri Institute of Medical Research |
| Copyright_xml | – notice: Tenri Foundation, Tenri Institute of Medical Research |
| DBID | AAYXX CITATION ADTOC UNPAY |
| DOI | 10.12936/tenrikiyo.27-009 |
| DatabaseName | CrossRef Unpaywall for CDI: Periodical Content Unpaywall |
| DatabaseTitle | CrossRef |
| DatabaseTitleList | |
| Database_xml | – sequence: 1 dbid: UNPAY name: Unpaywall url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/ sourceTypes: Open Access Repository |
| DeliveryMethod | fulltext_linktorsrc |
| EISSN | 2187-2244 |
| EndPage | 39 |
| ExternalDocumentID | 10.12936/tenrikiyo.27-009 10_12936_tenrikiyo_27_009 article_tenrikiyo_27_1_27_27_009_article_char_en |
| GroupedDBID | ALMA_UNASSIGNED_HOLDINGS JSF KQ8 MOJWN RJT AAYXX CITATION ABJNI ADTOC UNPAY |
| ID | FETCH-LOGICAL-c1729-aefd86e82c3e0185dc0a58d025340b70f71059879b50e972aa028c02f6a5780f3 |
| IEDL.DBID | UNPAY |
| ISSN | 1344-1817 2187-2244 |
| IngestDate | Sun Sep 07 11:20:45 EDT 2025 Tue Jul 01 03:59:47 EDT 2025 Wed Sep 03 06:30:36 EDT 2025 |
| IsDoiOpenAccess | true |
| IsOpenAccess | true |
| IsPeerReviewed | false |
| IsScholarly | true |
| Issue | 1 |
| Language | English |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c1729-aefd86e82c3e0185dc0a58d025340b70f71059879b50e972aa028c02f6a5780f3 |
| ORCID | 0009-0008-8281-1814 0000-0002-6451-3206 0000-0001-5787-2748 0000-0002-7475-2489 0000-0002-9736-3929 0000-0002-3397-4472 0000-0002-1460-6295 0000-0002-0839-7677 0000-0002-9034-8814 0000-0003-3846-441X 0009-0004-0882-0019 0000-0002-7099-7550 0000-0003-1248-9272 0000-0002-0153-9548 0009-0002-3198-7648 0000-0002-3030-123X |
| OpenAccessLink | https://proxy.k.utb.cz/login?url=http://doi.org/10.12936/tenrikiyo.27-009 |
| PageCount | 7 |
| ParticipantIDs | unpaywall_primary_10_12936_tenrikiyo_27_009 crossref_primary_10_12936_tenrikiyo_27_009 jstage_primary_article_tenrikiyo_27_1_27_27_009_article_char_en |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | 2024/12/25 2024-12-25 |
| PublicationDateYYYYMMDD | 2024-12-25 |
| PublicationDate_xml | – month: 12 year: 2024 text: 2024/12/25 day: 25 |
| PublicationDecade | 2020 |
| PublicationTitle | Tenri Medical Bulletin |
| PublicationTitleAlternate | Tenri Med Bull |
| PublicationYear | 2024 |
| Publisher | Tenri Foundation, Tenri Institute of Medical Research |
| Publisher_xml | – name: Tenri Foundation, Tenri Institute of Medical Research |
| References | 4) Takemoto Y, Suzuki Y, Tamakoshi A, et al. Epidemiology of X-linked adrenoleukodystrophy in Japan. J Hum Genet 2002;47:590-593. 2) Moser HW, Moser AB, Frayer KK, et al. Adrenoleukodystrophy: Increased plasma content of saturated very long chain fatty acids. Neurology 1981;31:1241-1249. 15) Mascalchi M. MRI CNS atrophy pattern and the etiologies of progressive ataxias. Tomography 2022;8:423-437. 24) Curé JK, Cromwell LD, Case JL, et al. Auditory dysfunction caused by multiple sclerosis: Detection with MR imaging. AJNR Am J Neuroradiol 1990;11:817-820. 20) Loes DJ, Hite S, Moser H, et al. Adrenoleukodystrophy: A scoring method for brain MR observations. AJNR Am J Neuroradiol 1994;15:1761-1766. 9) Choi JH, Kim HS, Oh EH, et al. Cerebello-brainstem dominant form of X-linked adrenoleukodystrophy with intrafamilial phenotypic variability. Front Neurol 2022;13:999419. 23) Scarpa A, Cassandro C, Vitale C, et al. A comparison of auditory and vestibular dysfunction in Parkinson's disease and Multiple System Atrophy. Parkinsonism Relat Disord 2020;71:51-57. 1) Mosser J, Douar AM, Sarde CO, et al. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 1993;361:726-730. 6) Loes DJ, Fatemi A, Melhem ER, et al. Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy. Neurology 2003;61:369-374. 10) Kim JH, Kim HJ. Childhood X-linked adrenoleukodystrophy: Clinical-pathologic overview and MR imaging manifestations at initial evaluation and follow-up. Radiographics 2005;25:619-631. 5) Engelen M, Kemp S, de Visser M, et al. X-linked adrenoleukodystrophy (X-ALD): Clinical presentation and guidelines for diagnosis, follow-up and management. Orphanet J Rare Dis 2012;7:51. 18) Ho ML, Moonis G, Ginat DT, et al. Lesions of the corpus callosum. AJR Am J Roentgenol 2013;200:W1-16. 26) Lu Z, Zhang B, Qiu W, et al. Comparative brain stem lesions on MRI of acute disseminated encephalomyelitis, neuromyelitis optica, and multiple sclerosis. PLoS One 2011;6:e22766. 3) Contreras M, Mosser J, Mandel JL, et al. The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane protein. FEBS Lett 1994;344:211-215. 11) Kumar AJ, Köhler W, Kruse B, et al. MR findings in adult-onset adrenoleukodystrophy. AJNR Am J Neuroradiol 1995;16:1227-1237. 13) Rueda-Lopes FC, Hygino da Cruz LC, Jr., Doring TM, et al. Diffusion-weighted imaging and demyelinating diseases: New aspects of an old advanced sequence. AJR Am J Roentgenol 2014;202:W34-42. 16) Okamoto K, Tokiguchi S, Furusawa T, et al. MR features of diseases involving bilateral middle cerebellar peduncles. AJNR Am J Neuroradiol 2003;24:1946-1954. 8) Ogaki K, Koga S, Aoki N, et al. Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: Case report and literature review. Neuropathology 2016;36:64-76. 21) Maillot O, Attyé A, Boyer E, et al. Post traumatic deafness: A pictorial review of CT and MRI findings. Insights Imaging 2016;7:341-350. 17) Uchino A, Sawada A, Takase Y, et al. Symmetrical lesions of the middle cerebellar peduncle: MR imaging and differential diagnosis. Magn Reson Med Sci 2004;3:133-140. 22) Hoche F, Seidel K, Brunt ER, et al. Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7). Neuropathol Appl Neurobiol 2008;34:479-491. 25) Cruz RA, Varkey T, Flavia A, et al. Hearing abnormalities in multiple sclerosis: Clinical semiology and pathophysiologic mechanisms. J Neurol 2022;269:2792-2805. 12) Chen YH, Lee YC, Tsai YS, et al. Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. PLoS One 2017;12:e0177296. 19) Bourekas EC, Varakis K, Bruns D, et al. Lesions of the corpus callosum: MR imaging and differential considerations in adults and children. AJR Am J Roentgenol 2002;179:251-257. 14) Andravizou A, Dardiotis E, Artemiadis A, et al. Brain atrophy in multiple sclerosis: Mechanisms, clinical relevance and treatment options. Auto Immun Highlights 2019;10:7. 7) Tan EK, Lim SH, Chan LL, et al. X-linked adrenoleukodystrophy: Spinocerebellar variant. Clin Neurol Neurosurg 1999;101:137-140. 22 23 24 25 26 10 11 12 13 14 M Mascalchi (15) 2022; 8 16 17 18 19 1 2 3 4 5 6 7 8 9 20 21 |
| References_xml | – reference: 21) Maillot O, Attyé A, Boyer E, et al. Post traumatic deafness: A pictorial review of CT and MRI findings. Insights Imaging 2016;7:341-350. – reference: 12) Chen YH, Lee YC, Tsai YS, et al. Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. PLoS One 2017;12:e0177296. – reference: 2) Moser HW, Moser AB, Frayer KK, et al. Adrenoleukodystrophy: Increased plasma content of saturated very long chain fatty acids. Neurology 1981;31:1241-1249. – reference: 3) Contreras M, Mosser J, Mandel JL, et al. The protein coded by the X-adrenoleukodystrophy gene is a peroxisomal integral membrane protein. FEBS Lett 1994;344:211-215. – reference: 16) Okamoto K, Tokiguchi S, Furusawa T, et al. MR features of diseases involving bilateral middle cerebellar peduncles. AJNR Am J Neuroradiol 2003;24:1946-1954. – reference: 7) Tan EK, Lim SH, Chan LL, et al. X-linked adrenoleukodystrophy: Spinocerebellar variant. Clin Neurol Neurosurg 1999;101:137-140. – reference: 17) Uchino A, Sawada A, Takase Y, et al. Symmetrical lesions of the middle cerebellar peduncle: MR imaging and differential diagnosis. Magn Reson Med Sci 2004;3:133-140. – reference: 20) Loes DJ, Hite S, Moser H, et al. Adrenoleukodystrophy: A scoring method for brain MR observations. AJNR Am J Neuroradiol 1994;15:1761-1766. – reference: 1) Mosser J, Douar AM, Sarde CO, et al. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 1993;361:726-730. – reference: 15) Mascalchi M. MRI CNS atrophy pattern and the etiologies of progressive ataxias. Tomography 2022;8:423-437. – reference: 5) Engelen M, Kemp S, de Visser M, et al. X-linked adrenoleukodystrophy (X-ALD): Clinical presentation and guidelines for diagnosis, follow-up and management. Orphanet J Rare Dis 2012;7:51. – reference: 10) Kim JH, Kim HJ. Childhood X-linked adrenoleukodystrophy: Clinical-pathologic overview and MR imaging manifestations at initial evaluation and follow-up. Radiographics 2005;25:619-631. – reference: 9) Choi JH, Kim HS, Oh EH, et al. Cerebello-brainstem dominant form of X-linked adrenoleukodystrophy with intrafamilial phenotypic variability. Front Neurol 2022;13:999419. – reference: 24) Curé JK, Cromwell LD, Case JL, et al. Auditory dysfunction caused by multiple sclerosis: Detection with MR imaging. AJNR Am J Neuroradiol 1990;11:817-820. – reference: 8) Ogaki K, Koga S, Aoki N, et al. Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: Case report and literature review. Neuropathology 2016;36:64-76. – reference: 4) Takemoto Y, Suzuki Y, Tamakoshi A, et al. Epidemiology of X-linked adrenoleukodystrophy in Japan. J Hum Genet 2002;47:590-593. – reference: 11) Kumar AJ, Köhler W, Kruse B, et al. MR findings in adult-onset adrenoleukodystrophy. AJNR Am J Neuroradiol 1995;16:1227-1237. – reference: 25) Cruz RA, Varkey T, Flavia A, et al. Hearing abnormalities in multiple sclerosis: Clinical semiology and pathophysiologic mechanisms. J Neurol 2022;269:2792-2805. – reference: 6) Loes DJ, Fatemi A, Melhem ER, et al. Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy. Neurology 2003;61:369-374. – reference: 18) Ho ML, Moonis G, Ginat DT, et al. Lesions of the corpus callosum. AJR Am J Roentgenol 2013;200:W1-16. – reference: 23) Scarpa A, Cassandro C, Vitale C, et al. A comparison of auditory and vestibular dysfunction in Parkinson's disease and Multiple System Atrophy. Parkinsonism Relat Disord 2020;71:51-57. – reference: 26) Lu Z, Zhang B, Qiu W, et al. Comparative brain stem lesions on MRI of acute disseminated encephalomyelitis, neuromyelitis optica, and multiple sclerosis. PLoS One 2011;6:e22766. – reference: 13) Rueda-Lopes FC, Hygino da Cruz LC, Jr., Doring TM, et al. Diffusion-weighted imaging and demyelinating diseases: New aspects of an old advanced sequence. AJR Am J Roentgenol 2014;202:W34-42. – reference: 14) Andravizou A, Dardiotis E, Artemiadis A, et al. Brain atrophy in multiple sclerosis: Mechanisms, clinical relevance and treatment options. Auto Immun Highlights 2019;10:7. – reference: 19) Bourekas EC, Varakis K, Bruns D, et al. Lesions of the corpus callosum: MR imaging and differential considerations in adults and children. AJR Am J Roentgenol 2002;179:251-257. – reference: 22) Hoche F, Seidel K, Brunt ER, et al. Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7). Neuropathol Appl Neurobiol 2008;34:479-491. – ident: 2 doi: 10.1212/WNL.31.10.1241 – ident: 5 doi: 10.1186/1750-1172-7-51 – ident: 10 doi: 10.1148/rg.253045118 – ident: 22 doi: 10.1111/j.1365-2990.2007.00933.x – ident: 23 doi: 10.1016/j.parkreldis.2020.01.018 – ident: 7 doi: 10.1016/S0303-8467(99)00028-1 – ident: 16 – ident: 25 doi: 10.1007/s00415-021-10915-w – ident: 17 doi: 10.2463/mrms.3.133 – ident: 19 doi: 10.2214/ajr.179.1.1790251 – ident: 21 doi: 10.1007/s13244-016-0490-9 – ident: 24 – ident: 1 doi: 10.1038/361726a0 – volume: 8 start-page: 423 issn: 2379-1381 year: 2022 ident: 15 publication-title: Tomography doi: 10.3390/tomography8010035 – ident: 20 – ident: 14 doi: 10.1186/s13317-019-0117-5 – ident: 6 doi: 10.1212/01.WNL.0000079050.91337.83 – ident: 12 doi: 10.1371/journal.pone.0177296 – ident: 26 doi: 10.1371/journal.pone.0022766 – ident: 3 doi: 10.1016/0014-5793(94)00400-5 – ident: 11 – ident: 13 doi: 10.2214/AJR.13.11400 – ident: 9 doi: 10.3389/fneur.2022.999419 – ident: 4 doi: 10.1007/s100380200090 – ident: 18 doi: 10.2214/AJR.11.8080 – ident: 8 doi: 10.1111/neup.12230 |
| SSID | ssj0003306028 |
| Score | 2.2804797 |
| Snippet | X-linked adrenoleukodystrophy (X-ALD) is classified into several clinical subtypes. Among them, the cerebello-brainstem-dominant form is rare, and its symptoms... |
| SourceID | unpaywall crossref jstage |
| SourceType | Open Access Repository Index Database Publisher |
| StartPage | 33 |
| SubjectTerms | auditory pathway cerebello-brainstem-dominant form magnetic resonance imaging (MRI) X-linked adrenoleukodystrophy (X-ALD) |
| Title | Adult-onset cerebello-brainstem-dominant form of X-linked adrenoleukodystrophy with auditory pathway involvement: A case report |
| URI | https://www.jstage.jst.go.jp/article/tenrikiyo/27/1/27_27-009/_article/-char/en http://doi.org/10.12936/tenrikiyo.27-009 |
| UnpaywallVersion | publishedVersion |
| Volume | 27 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| ispartofPNX | Tenri Medical Bulletin, 2024/12/25, Vol.27(1), pp.33-39 |
| journalDatabaseRights | – providerCode: PRVAFT databaseName: Open Access Digital Library customDbUrl: eissn: 2187-2244 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0003306028 issn: 1344-1817 databaseCode: KQ8 dateStart: 20120101 isFulltext: true titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html providerName: Colorado Alliance of Research Libraries |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1La9tAEF4au5BTm5KUOLRhDzm1rLORVo_tpZgSExoaGojBOZnZh8C10RpFJqiX_vXOWKqb0ELIRafRA83ufN_s7DfL2IkGJzPQmJaAxwTFpFroAieezROnnfYYDknv_O0qvZior9Nk-ne942H5HoEoPUXiWM0X8yYMo0xslHr9NEHW3WP9ydX30e0mn1JKIFCRMhoBKxOISqorYP73GY8g6OUPZGEkr99dlyto7mG5fAAw49dtt6O7TV9C2leyGK5rM7Q__-3a-OS377FXHcvko3ZYvGEvfLnPfo2o14ag7dM1t77yVHMIwtAhEdTOWbjQ7ovhRGR5KPhUUH3XOw6k9w5Lv14E19zVVUDncFrC5UCqjlA1nI42voeGz0sMeJsm5PUnPuIWUZK3hYkDNhmf33y5EN35C8IirdECfOHy1OeRjb1EXHdWQpI7ZEmxkiaTRUbkLM-0SaTXWQSAZMXKqEgB44As4resV4bSHzKeaThLjXTOqlgZ5zQoY0DHVhWQpxoG7MMfl8xWbZuNGaUn9B9n2_84i6hYrgfsc-u0rWk3yx5bntGlvWNrQFI2jAcD9nHr7affd_Qs63esV1dr_x65Sm2O2c7ldX7cDdbfSezwnw |
| linkProvider | Unpaywall |
| linkToUnpaywall | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1LS-RAEG5kFDypi4ojrvRhT0qPbdJ59F6WQRRZWPHgwHgaqh-BcYa0xAySvexf36pJdlRcEC85VR6kuuv7qqu_asa-aXAyA41pCXhMUEyqhS5w4tk8cdppj-GQ9M6_btLrkfo5TsYv6x2vy_cIROkZEsdqOps2YRBlYqnUW08TZN09tj66uR3eL_MppQQCFSmjEbAygaikugLmf5_xBoI2HpCFkbx-c1E-QvMM8_krgLnabrsdPS37EtK-ktlgUZuB_f2-a-OH377DtjqWyYftsPjC1ny5y_4MqdeGoO3TNbe-8lRzCMLQIRHUzlm40O6L4URkeSj4WFB91zsOpPcOc7-YBdc81VVA53BawuVAqo5QNZyONn6Ghk9LDHjLJuT1dz7kFlGSt4WJPTa6ury7uBbd-QvCIq3RAnzh8tTnkY29RFx3VkKSO2RJsZImk0VG5CzPtEmk11kEgGTFyqhIAeOALOJ91itD6Q8YzzScp0Y6Z1WsjHMalDGgY6sKyFMNfXbyzyWTx7bNxoTSE_qPk9V_nERULNd99qN12sq0m2VvLc_p0t6xMiApG8aDPjtdefvj9x1-yvqI9epq4b8iV6nNcTdM_wKrk--q |
| 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=Adult-onset+cerebello-brainstem-dominant+form+of+X-linked+adrenoleukodystrophy+with+auditory+pathway+involvement%3A+A+case+report&rft.jtitle=Tenri+Medical+Bulletin&rft.au=Yokota%2C+Yusuke&rft.au=Minami%2C+Akihiko&rft.au=Kawase%2C+Kango&rft.au=Taniguchi%2C+Takanori&rft.date=2024-12-25&rft.pub=Tenri+Foundation%2C+Tenri+Institute+of+Medical+Research&rft.issn=1344-1817&rft.eissn=2187-2244&rft.volume=27&rft.issue=1&rft.spage=33&rft.epage=39&rft_id=info:doi/10.12936%2Ftenrikiyo.27-009&rft.externalDocID=article_tenrikiyo_27_1_27_27_009_article_char_en |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1344-1817&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1344-1817&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1344-1817&client=summon |