Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Duriel I. Hardy"'
Publikováno v:
Journal of Pediatric Neurology. 20:052-056
Acute fulminant cerebral edema is a poorly understood but serious neurologic condition resulting in profound neurologic disability or mortality. Here we presented a case series of four children that presented to our institution with new neurologic dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d895c8515534c5bf5ac25f40c60eaf59
https://doi.org/10.1055/s-0041-1724099
https://doi.org/10.1055/s-0041-1724099
Publikováno v:
Neuropediatrics. 50:304-307
X-linked Charcot–Marie–Tooth disease (CMTX1) is the second most common form of Charcot–Marie–Tooth disease (CMT). It is caused by a mutation in the gap junction β 1 (GJB1) gene, which encodes for connexin-32. In addition to the peripheral ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b8997b5e556a594acbd3659f3210c9c
https://doi.org/10.1055/s-0039-1692982
https://doi.org/10.1055/s-0039-1692982
Autor:
Rui Xiao, Jeffrey S. Gerber, Sharon Stoll, Julia G. Harris, Yongdong Zhao, Sona Narula, Sabrina Gmuca, Amy Waldman, Duriel I Hardy, Pamela F. Weiss
Publikováno v:
Mult Scler Relat Disord
Background Neuromyelitis optica spectrum disorder (NMOSD) is a rare demyelinating disease in need of more studies to determine effective treatment regimens. The rarity of the disorder, however, makes large randomized-controlled trials challenging. Va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec07c3d1b1431df53366b92481da9e1
https://doi.org/10.1016/j.msard.2019.101488
https://doi.org/10.1016/j.msard.2019.101488