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Mohammad Abuawad
Mohammad Abuawad
Paris Diderot University
Genetics
Medicine
Alexander disease
Biology
Neuroscience
4
Papers
15
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Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy
2019
European Journal of Human Genetics
Chiara Aiello
Imen Dorboz
Cas Simons
Robert Thompson-Stone
Marcello Niceta
M. Elmaleh
Mohammad Abuawad
Diane Doummar
Alessandro Bruselles
Nicole I. Wolf
Lorena Travaglini
Odile Boespflug-Tanguy
Marco Tartaglia
Adeline Vanderver
Diana Rodriguez
Enrico Bertini
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Natural history of Alexander disease: A multicentric survey of 75 patients (reporting clinical, radiological and genetic characteristics in.)
2017
European Journal of Paediatric Neurology
Florence Renaldo
Cyril Mignot
Davide Tonduti
Diane Doummmar
Enrico Bertini
Stéphanie Paquay
Mohammad Abuawad
Imen Dorboz
Simon Samaan
Monique El Maleh
François Chalard
Odile Boespflug-Tanguy
Lydie Burglen
Diana Rodriguez
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Pathological changes in Alexander disease : a comparative study in human and mice with GFAP mutations
2017
Mohammad Abuawad
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Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy
2017
Brain
Imen Dorboz
Chiara Aiello
Cas Simons
Robert Thompson-Stone
Marcello Niceta
M Elmaleh
Mohammad Abuawad
Diane Doummar
Alessandro Bruselles
Nicole I. Wolf
Lorena Travaglini
Odile Boespflug-Tanguy
Marco Tartaglia
Adeline Vanderver
Diana Rodriguez
Enrico Bertini
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Citations (15)
1