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Publications by Makiko Hayashi
A Mutation of COX6A1 Causes a Recessive Axonal or Mixed Form of Charcot-Marie-Tooth Disease
American Journal of Human Genetics
Genetics
Amelioration of Inflammation and Tissue Damage in Sickle Cell Model Mice by Nrf2 Activation
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
A Severe Recessive and a Mild Dominant Form of Charcot-Marie-Tooth Disease Associated With a Newly Identified Glu222Lys GDAP1 Gene Mutation.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
Exome Sequencing Identifies a DYNC1H1 Mutation in a Large Pedigree With Dominant Axonal Charcot-Marie-Tooth Disease
American Journal of Human Genetics
Genetics
SET Binding Factor 1 (SBF1) Mutation Causes Charcot-Marie-Tooth Disease Type 4B3
Neurology
Neurology
MORC2mutations Cause Axonal Charcot-Marie-Tooth Disease With Pyramidal Signs
Annals of Neurology
Neurology
Charcot–Marie–Tooth Disease
Charcot-Marie-Tooth Disease. A Practical Guide
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Charcot-Marie-Tooth Disease Type 2R
Mutation Screening of Mitofusin 2 in Charcot-Marie-Tooth Disease Type 2
Journal of Neurology
Neurology
Update on Charcot-Marie-Tooth Disease
Current Neurology and Neuroscience Reports
Neuroscience
Neurology