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Archives of Physical Medicine and Rehabilitation, ISSN 0003-9993, 06/2019
OBJECTIVETo evaluate in a preliminary methodologic study, the Foot Function Index (FFI), a 3-subscale (pain, disability, and activity restriction) foot... 
Journal Article
Neurology, ISSN 0028-3878, 05/2018, Volume 90, Issue 19, pp. e1706 - e1710
OBJECTIVETo describe in detail the clinical profile of Charcot-Marie-Tooth disease subtype 3 (CMTX3) to aid appropriate genetic testing and rehabilitative... 
HETEROGENEITY | MARIE-TOOTH DISEASE | NEUROPATHIES | CLINICAL NEUROLOGY
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 09/2016, Volume 93, p. 201
Mice heterozygously deficient for the myelin protein P.sub.0 gene (P.sub.0 +/-) develop a slowly progressing neuropathy modeling demyelinating... 
Charcot-Marie-Tooth disease | Analysis
Journal Article
Muscle & Nerve, ISSN 0148-639X, 09/2019, Volume 60, Issue 3, pp. 219 - 221
See article on pages 242–249 in this issue . 
Disease control | Charcot-Marie-Tooth disease | Index Medicus
Journal Article
Nature Reviews Drug Discovery, ISSN 1474-1776, 06/2018, Volume 17, Issue 6, pp. 391 - 391
Journal Article
NEUROLOGY, ISSN 0028-3878, 05/2012, Volume 78, Issue 22, pp. 1714 - 1720
Objective: To identify the gene responsible for 14q32-linked dominant spinal muscular atrophy with lower extremity predominance (SMA-LED, OMIM 158600).... 
TRANSPORT | DEFECTS | GENE | DYNEIN | TRPV4 | MOUSE MODEL | MOTOR | MARIE-TOOTH DISEASE | DISORDERS | AMYOTROPHIC-LATERAL-SCLEROSIS | CLINICAL NEUROLOGY
Journal Article
ISSN 1932-6203, 2017
Charcot-Marie-Tooth (CMT) disease or hereditary motor and sensory neuropathy is the most prevalent inherited peripheral neuropathy and is associated with over... 
Pathology | Axons | Charcot-Marie-Tooth disease | Nerves, Peripheral--Diseases | Neuropathy
Journal Article
Cancer Research, ISSN 0008-5472, 10/2018, Volume 78, Issue 20, pp. 5780 - 5792
Triple-negative breast cancer (TNBC) is the most lethal subtype of breast cancer, with a high propensity for distant metastasis and limited treatment options,... 
PROTEIN INTERACTIONS | DOMAIN | ONCOLOGY | MARIE-TOOTH DISEASE | EXPRESSION | SOMATIC MUTATIONS | GENOME
Journal Article
ISSN 1364-6745, 2017
Charcot-Marie-Tooth disease (CMT) refers to a genetically heterogeneous group of disorders which cause a peripheral motor and sensory neuropathy. The overall... 
MFN2 | CMT2A | mosaicism | Charcot-Marie-tooth disease
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1
There was a spelling error in the name of the seventh author. (2012) Correction: The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2... 
Charcot-Marie-Tooth disease
Journal Article
Journal of the Peripheral Nervous System, ISSN 1085-9489, 03/2019, Volume 24, Issue 1, pp. 161 - 161
Journal Article
Neurophysiologie Clinique = Clinical Neurophysiology, ISSN 0987-7053, 06/2019, Volume 49, Issue 3, p. 200
Contexte L'association de mouvements anormaux avec une atteinte du nerf périphérique doit faire évoquer un certain nombre de diagnostics, guidés par les... 
Mitochondria | Charcot-Marie-Tooth disease | Myelin-associated glycoprotein
Journal Article
Experimental Neurology, ISSN 0014-4886, 10/2019, Volume 320, pp. 113004 - 113004
Mutations in the mitochondrial outer membrane gene cause Charcot-Marie-Tooth (CMT) neuropathy. Reduction or absence of GDAP1 has been associated with abnormal... 
Axonopathy | Neuroinflammation | Gdap1 knockout mouse | GDAP1 | Charcot-Marie-tooth disease | Index Medicus
Journal Article
JAMA NEUROLOGY, ISSN 2168-6149, 05/2019, Volume 76, Issue 5, pp. 621 - 622
A 13-year-old boy with a longstanding history of gait imbalance presented with 2 episodes of acute-onset left hemibody weakness and dysarthria without changes... 
MARIE-TOOTH DISEASE | RECURRENT | TRANSIENT | CLINICAL NEUROLOGY | Gait | Abnormalities | Index Medicus | Abridged Index Medicus
Journal Article
NATURE REVIEWS NEUROSCIENCE, ISSN 1471-0048, 04/2010, Volume 11, Issue 4, pp. 275 - 283
In addition to their role in providing myelin for rapid impulse propagation, the glia that ensheath long axons are required for the maintenance of normal axon... 
CENTRAL WHITE-MATTER | MULTIPLE-SCLEROSIS LESIONS | MARIE-TOOTH-DISEASE | SHIVERER MOUSE | GAP-JUNCTIONS | HEREDITARY SPASTIC PARAPLEGIA | RAT OPTIC-NERVE | INHERITED DEMYELINATING NEUROPATHIES | PROTEIN TRANSFER HYPOTHESIS | NEUROSCIENCES | SQUID GIANT-AXON
Journal Article
Cytoskeleton (Hoboken, N.J.), ISSN 1949-3584, 11/2017, Volume 74, Issue 11, pp. 405 - 419
Formins are a family of regulators of actin and microtubule dynamics that are present in almost all eukaryotes. These proteins are involved in many cellular... 
actin | INF2 | Charcot-Marie-Tooth disease | FHDC1 | focal segmental glomerulosclerosis
Journal Article
Neurophysiologie Clinique, ISSN 0987-7053, 09/2018, Volume 48, Issue 4, pp. 224 - 224
Journal Article
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