Results 91 to 100 of about 306,111 (180)

Juvenile Alexander Disease: A Rare Leukodystrophy. [PDF]

Cureus, 2022
Ullah R, Wazir MH, Gul A, Gul F, Arshad A.   +4 more
europepmc   +1 more source

Association Between Rapid Progression, Early Mortality, and Imaging in Neonatal-Onset Alexander Disease. [PDF]

Neuropediatrics
Schwarz S, Steggerda SJ, de Vries LS, Schulz K, Dürr NR, Lequin MH, Rosenbaum T, Felderhoff-Müser U, Jauss RT, Brevis Nuñes F, Bruns N.   +10 more
europepmc   +1 more source

STAT3 Drives GFAP Accumulation and Astrocyte Pathology in a Mouse Model of Alexander Disease. [PDF]

Cells, 2023
Hagemann TL, Coyne S, Levin A, Wang L, Feany MB, Messing A.   +5 more
europepmc   +1 more source

Calcium pyrophosphate crystal deposition disease: diagnosis and treatment

, 2014
José Luis Rosales-Alexander,1 Jerónimo Balsalobre Aznar,1 César Magro-Checa2 1Rheumatology Department, Hospiten Ramblas, Santa Cruz de Tenerife, 2Rheumatology Department, San Cecilio University Hospital, Granada, Spain Abstract ...
Rosales-Alexander JL, Balsalobre Aznar J, Magro-Checa C   +2 more
core  

Prevalence of Elevated Opening Pressure Measurements in Alexander Disease. [PDF]

Pediatr Neurol
Joung JY, Gallison KJ, Liu GW, Berger JA, Drum ET, Dubow SR, McClung HA, Faig W, Avery RA, Liu GT, Narula S, Vossough A, Waldman AT.   +12 more
europepmc   +1 more source

Corrigendum to "Alexander disease mutations differentially sensitize glial fibrillary acidic protein (GFAP) to posttranslational modifications and network disruption by oxidants" [Redox Biology 92 (2026) 104103]. [PDF]

Redox Biol
Goya-Iglesias N, Hägglund P, Martínez-Cenalmor P, Nybo T, Lorentzen LG, Pajares MA, Davies MJ, Pérez-Sala D.   +7 more
europepmc   +1 more source

Bilateral vestibulopathy in Alexander disease type II- a case report. [PDF]

Eur Arch Otorhinolaryngol
Hofmann JB, Gautschi M, Vossenkaul A, Blanquet M, Bremova-Ertl T.   +4 more
europepmc   +1 more source

Alexander disease: models, mechanisms, and medicine. [PDF]

Curr Opin Neurobiol, 2022
Hagemann TL.
europepmc   +1 more source

Alexander disease mutations differentially sensitize glial fibrillary acidic protein (GFAP) to posttranslational modifications and network disruption by oxidants. [PDF]

Redox Biol
Goya-Iglesias N, Hägglund P, Martínez-Cenalmor P, Nybo T, Lorentzen LG, Pajares MA, Davies MJ, Pérez-Sala D.   +7 more
europepmc   +1 more source

Alexander disease

, 2008
Frank Gaillard, Rohit Sharma, Travis Fahrenhorst-Jones   +2 more
openaire   +1 more source