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Publications by Michael G. Hanna
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome
American Journal of Human Genetics
Genetics
Biallelic Mutations in ADPRHL2 , Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome
American Journal of Human Genetics
Genetics
Pathogenic TFG Mutations Underlying Hereditary Spastic Paraplegia Impair Secretory Protein Trafficking and Axon Fasciculation
Cell Reports
Biochemistry
Genetics
Molecular Biology
Mutations in GFAP Disrupt the Distribution and Function of Organelles in Human Astrocytes
Cell Reports
Biochemistry
Genetics
Molecular Biology
Spider Toxin Inhibits Gating Pore Currents Underlying Periodic Paralysis
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Skeletal Muscle MRI Differentiates SBMA and ALS and Correlates With Disease Severity
Neurology
Neurology
Familial Childhood-Onset Progressive Cerebellar Syndrome Associated With theATP1A3mutation
Neurology: Genetics
Neurology
Genetics
A Novel KCNA1 Mutation in a Family With Episodic Ataxia and Malignant Hyperthermia
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
Myotonia in a Patient With a Mutation in an S4 Arginine Residue Associated With Hypokalaemic Periodic Paralysis and a Concomitant Synonymous CLCN1 Mutation
Scientific Reports
Multidisciplinary
Sodium and Chloride Channelopathies With Myositis: Coincidence or Connection?
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
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