Zobrazeno 1 - 10
of 322
pro vyhledávání: '"Stroke-like episode"'
Autor:
Josef Finsterer
Publikováno v:
European Journal of Case Reports in Internal Medicine (2024)
Externí odkaz:
https://doaj.org/article/a94c65d1c0444f9ea2829fabcec1aa20
Publikováno v:
Epilepsy & Behavior Reports, Vol 25, Iss , Pp 100652- (2024)
Behr syndrome is associated with compound heterozygous dysfunction in OPA1 gene and typically presents with a constellation of visual impairment due to early onset optic atrophy, cerebellar ataxia, peripheral neuropathy, deafness, and gastrointestina
Externí odkaz:
https://doaj.org/article/78b9d9378d2742c094878487005013ee
Autor:
Josef Finsterer
Publikováno v:
Clinical Case Reports, Vol 11, Iss 10, Pp n/a-n/a (2023)
Externí odkaz:
https://doaj.org/article/b25e0e1da2a44564a56b1d2382e88ff6
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-7 (2022)
Abstract Background Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episode syndrome is a rare mitochondrial genetic disorder that can present with a variety of clinical manifestations, including stroke, hearing loss, seizures, and
Externí odkaz:
https://doaj.org/article/0ecab714f84d499fa5d3e0eca9e66034
Publikováno v:
Annals of Indian Academy of Neurology, Vol 26, Iss 6, Pp 980-982 (2023)
Coenzyme q10 (CoQ10) deficiency is an extremely uncommon disease that has very rarely been reported in adulthood. This case describes an elderly male with ataxia since adolescence, and visual disturbance since 40, presenting with recurrent episodes o
Externí odkaz:
https://doaj.org/article/02413efc558947eca4cc7631016f5244
Autor:
Josef Finsterer, Sounira Mehri
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Externí odkaz:
https://doaj.org/article/e4076e0b697d4006a872d2e5678dd2ae
Autor:
Josef Finsterer
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 4, Iss , Pp 100160- (2023)
Externí odkaz:
https://doaj.org/article/8e519da19142448c8d00bdf4dcfc489b
Autor:
Josef Finsterer
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Externí odkaz:
https://doaj.org/article/9766d81437174184a6b20b870c62f416
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract Mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS) is characterized by metabolic stroke, seizures, cognitive decline, lactic acidosis, ragged‐red fibers, headache, and vomiting, and in 80% of cases due to the
Externí odkaz:
https://doaj.org/article/14edd0da662543a29c068e6f62c55f42
Autor:
Fumiya Kutsuna, Yohei Tateishi, Kairi Yamashita, Tadashi Kanamoto, Takuro Hirayama, Tomoaki Shima, Atsushi Nagaoka, Shunsuke Yoshimura, Teiichiro Miyazaki, Jun Sone, Tsuyoshi Izumo, Akira Tsujino
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 3, Iss , Pp 100127- (2022)
Neuronal intranuclear inclusion disease (NIID) is a slowly progressive neurodegenerative disease. Some patients with NIID occasionally present with acute symptoms. However, its mechanism remains unclear. We report a patient with NIID who presented wi
Externí odkaz:
https://doaj.org/article/60a15549879848e2970c5a2725a5d2c4