Keywords: Charcot-Marie-Tooth disease; Mitochondria; Mitochondrial fission; Mitochondrial fusion; DRP1; OPA1; MFN1; MFN2; GDAP1; Neurodegeneration; Charcot-Marie-Tooth disease; Dominant Optic Atrophy; Neuronal maturation; Neuronal plasticity; Synapse; Dendrite; Axon;
مقالات ISI Charcot-Marie-Tooth disease (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Large and small sensory fibers; Muscle weakness; Balance impairment; Rehabilitation;
Keywords: Charcot-Marie-Tooth disease; Action potential; Nerve conduction study; Sensory nerve action potential; Compound muscle action potential; Ion channel; Voltage-gated sodium channel; Voltage-gated potassium channel; Node of Ranvier; Paranode; Juxtaparanode; Septate-like junction; Tight
Keywords: Charcot-Marie-Tooth disease; Parkinson's disease; Mitophagy; Charcot-Marie-Tooth disease; Amyotrophic lateral; Sclerosis;
Keywords: Charcot-Marie-Tooth disease; Giant Axonal Neuropathy; GAN; Gigaxonin; Charcot-Marie-Tooth disease; Straight hair; Gross Motor Function Measure;
Keywords: Charcot-Marie-Tooth disease; Aβ; amyloid β; AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; APP; amyloid precursor protein; AR; androgen receptor; BICD; Bicaudal D; BDNF; brain-derived neurotrophic factor; BMP; bone morphogenetic protein; CAV2; Canine Adenovirus 2; CMT
A novel homozygous nonsense mutation in NEFL causes autosomal recessive Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; NEFL; Charcot-Marie-Tooth disease; Autosomal recessive; Homozygous mutation;
Case studyCranial nerve involvement in Charcot-Marie-Tooth Disease
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth Disease; Cranial nerves; Trigeminal nerve;
Case reportBrain involvement in Charcot-Marie-Tooth disease due to ganglioside-induced differentiation associated-protein 1 mutation
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Neuropathy; GDAP1; Brain abnormality;
Case reportConfirmation of the GNB4 gene as causal for Charcot-Marie-Tooth disease by a novel de novo mutation in a Czech patient
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; De novo; Whole exome sequencing; GNB4;
Similar clinical, pathological, and genetic features in Chinese patients with autosomal recessive and dominant Charcot-Marie-Tooth disease type 2K
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; GDAP1; Chinese population; Axonal CMT;
Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene
Keywords: Charcot-Marie-Tooth disease; Distal hereditary motor neuropathy; Charcot-Marie-Tooth disease; HSPB1; Neuromuscular disease; Peripheral neuropathy;
Deterioration in gait and functional ambulation in children and adolescents with Charcot-Marie-Tooth disease over 12 months
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Gait; Functional ambulation; Paediatrics; Longitudinal;
Responsiveness of gait analysis parameters in a cohort of 71 CMT subjects
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Outcome measures; Responsiveness; Gait analysis; Clinical trials;
Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2
Keywords: Charcot-Marie-Tooth disease; IGHMBP2; Next-generation sequencing; Charcot-Marie-Tooth disease; Hereditary sensory and motor neuropathy; Spinal muscular atrophy with respiratory distress 1;
Coexistence of Charcot Marie Tooth disease type 1A and diabetes in Taiwan: A clinicopathological study
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; CMT1A; Peripheral myelin protein 22; Diabetes; Sural nerve biopsy; Myelin; Morphometry;
The insertion domain 1 of class IIA dimeric glycyl-tRNA synthetase is a rubredoxin-like zinc ribbon
Keywords: Charcot-Marie-Tooth disease; Glycyl-tRNA synthetase; Ap4A; Zinc finger; Insertion domain 1; Aminoacyl tRNA synthetase; Hereditary motor neuropathy; Charcot-Marie-Tooth disease;
Clinical spectrum and gender differences in a large cohort of Charcot-Marie-Tooth type 1A patients
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Hereditary neuropathy; Clinical spectrum; Disability; Quality of life; Gender;
Quality-of-life in Charcot-Marie-Tooth disease: The patient's perspective
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Quality of life; Patient reported outcomes; Peripheral neuropathy;
CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila
Keywords: Charcot-Marie-Tooth disease; Drosophila; Aminoacyl-tRNA synthetase; Charcot-Marie-Tooth disease;
Mutational analysis of the 5â² non-coding region of GJB1 in a Taiwanese cohort with Charcot-Marie-Tooth neuropathy
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; CMT; HMSN; GJB1; CX32; 5â² non-coding region; Promoter;
A comprehensive evaluation of the variation in ankle function during gait in children and youth with Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Gait analysis; Kinematics; Kinetics; Gait patterns;
A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; CMT2L; Exome; HSPB8; HSP22; Korean;
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age
Keywords: Charcot-Marie-Tooth disease; CMT; Charcot Marie Tooth disease; Cra; Cramping allele of the Dync1h1 gene (p.Y1055C mutation); IPGTT; intra-peritoneal glucose tolerance test; LPL; lipoprotein lipase; MEF; mouse embryonic fibroblast; MFN; mitofusin; PPARα; peroxisome proliferation acti
Hand weakness in Charcot-Marie-Tooth disease 1X
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Connexin 32; Hand strength; Overwork weakness; Neuropathy; GJB1;
X inactivation in females with X-linked Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; GJB1; Connexin32; X inactivation;
Exploring the experience of fatigue in people with Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; Muscle fatigue; Charcot-Marie-Tooth disease; Exercise; Experienced fatigue;
Gait pattern classification in children with Charcot-Marie-Tooth disease type 1A
Keywords: Charcot-Marie-Tooth disease; Gait analysis; Charcot-Marie-Tooth disease; Gait patterns; Cluster analysis; Toe walking; Heel walking;
Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot-Marie-Tooth type 2
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; CMT2A; Hereditary motor and sensory neuropathy; MFN2; R104W mutation;
Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: Results from a multitask locomotor protocol
Keywords: Charcot-Marie-Tooth disease; Gait analysis; Reliability; Charcot-Marie-Tooth disease; Outcome measures; Toe walking; Heel walking; Step ascending/descending;
Canine inherited motor and sensory neuropathies: An updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease
Keywords: Charcot-Marie-Tooth disease; Inherited motor and sensory neuropathy; Canine; Charcot-Marie-Tooth disease; Peripheral nervous system; Genetic mutation;
An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations
Keywords: Charcot-Marie-Tooth disease; ARS; aminoacyl-tRNA synthetase; GARS; glycyl-tRNA synthetase; YARS; tyrosyl-tRNA synthetase; AARS; alanyl-tRNA synthetase; CMT; Charcot-Marie-Tooth disease; Wlds; Wallerian Degeneration Slow; HSMN; hereditary sensory and motor neuropathy; DI-CMTC; dom
Hypothesis of double polarization
Keywords: Charcot-Marie-Tooth disease; Schwann cell; Oligodendrocyte; Myelin; Myelination; Axon; Axonal degeneration; Charcot-Marie-Tooth disease; Intracellular trafficking; Axonal transport; Schmidt-Lanterman incisure; Paranodal loop;
136th ENMC International Workshop: Charcot-Marie-Tooth Disease Type 1A (CMT1A)8-10 April 2005, Naarden, The Netherlands
Keywords: Charcot-Marie-Tooth disease; Charcot-Marie-Tooth disease; Ascorbic acid; Peripheral Myelin Protein 22 (PMP22); Hereditary neuropathy; Clinical trial;