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2016, ISBN 3319432915, 497
eBook
by Li, Jun
Experimental neurology, ISSN 0014-4886, 05/2015, Volume 267, pp. 209 - 218
Charcot–Marie–Tooth disease | Action potential | Voltage-gated potassium channel | Polyneuropathy | CMT1A | Voltage-gated sodium channel | Nerve conduction study | Demyelination | CMT2 | CMTX1 | Compound muscle action potential | Inherited neuropathy | Sensory nerve action potential | Axonal degeneration | Hereditary neuropathy with liability to pressure palsies | Septate-like junction | HNPP | Caspr | Ion channel | Paranode | Adherens junction | Juxtaparanode | Connexin-1 | Myelination | Node of Ranvier | PMP22 | Tight junction | Charcot-Marie-Tooth disease | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Action Potentials - genetics | Animals | Neural Conduction - genetics | Nerve Fibers, Myelinated - pathology | Rodentia | Peripheral Nervous System Diseases - pathology | Peripheral Nervous System Diseases - physiopathology | Myelin Proteins - metabolism | Peripheral Nervous System Diseases - genetics | Disease Models, Animal | Physiological aspects | Myelin proteins | Index Medicus | inherited neuropathy | voltage-gated potassium channel | sensory nerve action potential | voltage-gated sodium channel | connexin-1 | adherens junction | ion channel | demyelination | tight junction | septate-like junction | polyneuropathy | nerve conduction study | axonal degeneration | action potential | node of Ranvier | compound muscle action potential | paranode | juxtaparanode | hereditary neuropathy with liability to pressure palsies | myelination
Journal Article