Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Leukoencephalopathy with neuroaxonal spheroids"'
Publikováno v:
Diagnostics, Vol 13, Iss 6, p 1018 (2023)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia encompasses hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented orthochromatic leukodystrophy. We describe the clinicopathological and genetic findings of
Externí odkaz:
https://doaj.org/article/a42e6c822a124026af9798fd460a028d
Akademický článek
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Autor:
Michal Lubomski, Penelope J Spring, Irene Yew Lan Tan, Barry Kane, Joanne Sy, Heng Wei, Michael E. Buckland
Publikováno v:
Journal of the Neurological Sciences. 395:25-28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ab4bf021f582bf56cc5cfdfb769c7fd
https://doi.org/10.1016/j.jns.2018.09.025
https://doi.org/10.1016/j.jns.2018.09.025
Autor:
Yukihiko Washimi, Kazuhiro Fukushima, Ken Ichi Hoshi, Nobuo Araki, Ikuru Yazawa, Michiaki Kinoshita, Shu-ichi Ikeda, Yasufumi Kondo, Ban-yu Saitoh, Jun Ichi Kira, Kunihiro Yoshida, Keisuke Ishizawa
Publikováno v:
INTERNAL MEDICINE. 53(1):21-27
Objective Hereditary diffuse leukoencephalopathy with neuroaxonal spheroids (HDLS) is an adult-onset white matter disease that presents clinically with cognitive, mental and motor dysfunction. Several autopsy reports have indicated that the corpus ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c84af60e32af564cfc58c11669752d3b
https://soar-ir.repo.nii.ac.jp/records/3678
https://soar-ir.repo.nii.ac.jp/records/3678
Autor:
Peter Hedera, Adam M. Wegner, Siddharama Pawate, Subramaniam Sriram, Kirk Kleinfeld, Bret C. Mobley
Publikováno v:
Journal of Neurology. 260:558-571
The objective of this work is to report on a series of five patients with adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia (ALSP). ALSP is a rare adult-onset leukodystrophy, which encompasses hereditary diffuse leukoencep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9a9ebe90d19b3fe8b579c6abfab3493
https://doi.org/10.1007/s00415-012-6680-6
https://doi.org/10.1007/s00415-012-6680-6
Autor:
Heng Wei, Irene Tan, Michael E. Buckland, Michal Lubomski, Joanne Sy, Barry Kane, Penelope J Spring
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 89:A16.1-A16
IntroductionWe present an unusual case of adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia (ALSP) mimicking systemic lupus erythematosus (SLE) cerebral vasculitis. ALSP is an autosomal dominant progressive leukodystrophy,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a85c543a131ad82b12b13b4e92a0db04
https://doi.org/10.1136/jnnp-2018-anzan.37
https://doi.org/10.1136/jnnp-2018-anzan.37
Autor:
Zbigniew K. Wszolek, J.A. Van Gerpen, Daniel F. Broderick, Dennis W. Dickson, Christian Wider, L. Brown
Publikováno v:
Neurology. 71:925-929
Objective: To report a new American family with hereditary diffuse leukoencephalopathy with spheroids (HDLS), including serial, presymptomatic and symptomatic, cranial MRIs from the proband. Methods: We report clinical and genealogic investigations o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e91d1f3ce5f08df9318d711e09da614c
https://doi.org/10.1212/01.wnl.0000325916.30701.21
https://doi.org/10.1212/01.wnl.0000325916.30701.21
Autor:
Claudia F. Lucchinetti, B. M. Keegan, K. A. Josephs, Joseph E. Parisi, B. F. Boeve, Caterina Giannini
Publikováno v:
Neurology. 70:1128-1133
Background: Leukoencephalopathy with neuroaxonal spheroids is a rare cause of severe, subacute dementia that usually presents in childhood and is inherited in an autosomal dominant pattern. The authors present clinical, radiologic, and pathologic fea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2e5b529ad3c5944b0bd7c070cb47c37
https://doi.org/10.1212/01.wnl.0000304045.99153.8f
https://doi.org/10.1212/01.wnl.0000304045.99153.8f
Akademický článek
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Autor:
Peter A. Calabresi, John N. Ratchford
Publikováno v:
Neurology. 70:1071-1072
The most common imitators of multiple sclerosis (MS) are other autoimmune diseases and infections; however, an increasing number of metabolic diseases have been recognized as uncommon mimics of MS (table). While MRI has revolutionized the diagnosis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::725c4397e2446a0de62405d8d74fd1fd
https://doi.org/10.1212/01.wnl.0000307667.44679.32
https://doi.org/10.1212/01.wnl.0000307667.44679.32