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pro vyhledávání: '"anti-glutamic acid decarboxylase antibodies"'
Akademický článek
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Autor:
Joana Jesus‐Ribeiro, Alireza Bozorgi, Modhi Alkhaldi, Mahmoud Shaqfeh, Guadalupe Fernandez‐Baca Vaca, Bashar Katirji
Publikováno v:
Clinical Case Reports, Vol 8, Iss 1, Pp 61-64 (2020)
Abstract Epilepsy should be suspected in patients with Stiff‐person syndrome and new onset paroxysmal episodes. Musicogenic epilepsy may be a manifestation of anti‐GAD‐Ab spectrum, supporting an autoimmune workup in these patients. Appropriate
Externí odkaz:
https://doaj.org/article/0183b66c7272427388d8c09c8da9dff3
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Progressive encephalomyelitis with rigidity and myoclonus (PERM) is part of the variant type of the Stiff Person Syndrome (SPS) and is a rare neurological disease. We report here a patient with PERM who had thymoma and was positive for anti-glutamic
Externí odkaz:
https://doaj.org/article/bf293a1d2b7a4293823b21167b0afc55
Autor:
Joe Smith, Hayley Storey
Publikováno v:
British and Irish Orthoptic Journal, Vol 15, Iss 1 (2019)
Aim: To report a case of sudden onset vertical diplopia, blurred vision, and muscle spasms. Methods: This is a case report of a 57-year-old female who presented to the accident and emergency department with a one day history of vertical diplopia and
Externí odkaz:
https://doaj.org/article/109a8f11725c4f2eabc769f56695a439
Autor:
Alireza Bozorgi, Mahmoud Shaqfeh, Guadalupe Fernandez-Baca Vaca, Modhi Alkhaldi, Bashar Katirji, Joana Jesus-Ribeiro
Publikováno v:
Clinical Case Reports, Vol 8, Iss 1, Pp 61-64 (2020)
Clinical Case Reports
Clinical Case Reports
Epilepsy should be suspected in patients with Stiff‐person syndrome and new onset paroxysmal episodes. Musicogenic epilepsy may be a manifestation of anti‐GAD‐Ab spectrum, supporting an autoimmune workup in these patients. Appropriate treatment
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Frontiers in Neurology
Frontiers in Neurology
Progressive encephalomyelitis with rigidity and myoclonus (PERM) is part of the variant type of the Stiff Person Syndrome (SPS) and is a rare neurological disease. We report here a patient with PERM who had thymoma and was positive for anti-glutamic
Publikováno v:
European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, Elsevier, 2018, 22 (3), pp.548--551. ⟨10.1016/j.ejpn.2018.01.004⟩
European Journal of Paediatric Neurology, Elsevier, 2018, 22 (3), pp.548--551. ⟨10.1016/j.ejpn.2018.01.004⟩
International audience; Introduction Anti-glutamic acid decarboxylase (anti-GAD65) antibodies are a rare cause of autoimmune encephalitis. This entity is mainly recognized in adults and very few cases were reported in children. We report on a paediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f1be7e2b29e7df0298f3906af94d071
https://hal.archives-ouvertes.fr/hal-01876256
https://hal.archives-ouvertes.fr/hal-01876256
Autor:
Takagi Masahito, Yamasaki Hiroshi, Endo Keiko, Yamada Tetsuya, Kaneko Keizo, Oka Yoshitomo, Mori Etsuro
Publikováno v:
BMC Neurology, Vol 11, Iss 1, p 156 (2011)
Abstract Background Glutamic acid decarboxylase (GAD) is the rate-limiting enzyme for producing γ-aminobutyric acid, and it has been suggested that antibodies against GAD play a role in neurological conditions and type 1 diabetes. However, it is not
Externí odkaz:
https://doaj.org/article/d1bf6a19be1f4fa4ad7153fc2416dd30
Akademický článek
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Akademický článek
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