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Neuromuscular Disorders : NMD|January 16, 2019
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Handbook of Clinical Neurology|January 13, 2018
Towards precision medicineTanya Bardakjian, Pedro Gonzalez-Alegre
Journal of the Peripheral Nervous System : JPNS|March 8, 2019
POLG mutations presenting as Charcot-Marie-Tooth diseaseJade Phillips, Steve Courel, Adriana P Rebelo, et al.
The Journal of Cell Biology|January 10, 2002
Myelination: some receptors requiredSteven S Scherer
Neuron|September 20, 2006
Inherited neuropathies: new genes don't fit old modelsSteven S Scherer
The Journal of Clinical Investigation|November 3, 2011
The debut of a rational treatment for an inherited neuropathy?Steven S Scherer
Annals of the New York Academy of Sciences|November 1, 2017
Nodes, Paranodes, and Incisures: From Form to FunctionSteven S Scherer
Neuro-Ophthalmology (Aeolus Press)|October 5, 2020
Contrast Acuity and the King-Devick Test in Huntington's DiseaseAli G Hamedani, Tanya Bardakjian, Laura J Balcer, et al.
Cold Spring Harbor Perspectives in Biology|January 22, 2024
Peripheral Nervous System (PNS) Myelin DiseasesSteven S Scherer, John Svaren
Glia|September 23, 2008
Molecular mechanisms of inherited demyelinating neuropathiesSteven S Scherer, Lawrence Wrabetz
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