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Publications by H Abdel-Hamid

Mutations in LAMB2 Causing a Severe Form of Synaptic Congenital Myasthenic Syndrome

Journal of Medical Genetics

English

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Congenital Myasthenic Syndrome Due to DOK7 Mutations in a Family From Chile

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Electrophysiological Study in Synaptic Congenital Myasthenic Syndrome: End-Plate Acetylcholinesterase Deficiency

Arquivos de Neuro-Psiquiatria

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Congenital Myasthenic Syndrome Due to Mutation in CHRNE Gene

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Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome With a Homozygous Null Mutation

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ENU Induced Mutations Causing Congenital Cardiovascular Anomalies

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Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans

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Congenital Myasthenic Syndromes

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Congenital Myasthenic Syndromes

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A Neonate With MuSK Congenital Myasthenic Syndrome Presenting With Refractory Respiratory Failure

Frontiers in Pediatrics

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