Keywords: ارثی و نوروپاتی حسی; CMT; Charcot Marie Tooth disease; AD; Autosomal dominant; AR; Autosomal recessive; MNCV; Motor nerve conduction velocity; CMAP; Compound muscle action potential; PMP22; Peripheral myelin protein 22; HMSN; Hereditary motor sensory neuropathy; LITAF; lipopo
مقالات ISI ارثی و نوروپاتی حسی (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: ارثی و نوروپاتی حسی; Charcot-Marie-Tooth disease; Hereditary motor and sensory neuropathy; Hand strength; Manual dexterity; Sensory function
Pmp22 mutant allele-specific siRNA alleviates demyelinating neuropathic phenotype in vivo
Keywords: ارثی و نوروپاتی حسی; CMT; Charcot-Marie-Tooth disease; siRNA; small interfering RNA; PMP22; peripheral myelin protein 22Â kD; MBP; myelin basic protein; MPZ; myelin protein zero; IPN; Inherited peripheral neuropathy; HMSN; hereditary motor and sensory neuropathy; HNPP; heredi
Atypical presentation of Charcot–Marie–Tooth disease 1A: A case report
Keywords: ارثی و نوروپاتی حسی; Charcot–Marie–Tooth disease; Hereditary motor and sensory neuropathy; PMP22 gene; Charcot–Marie–Tooth 1A; Asymmetry; Cranial nerve involvement
Novel mitofusin 2 splice-site mutation causes Charcot-Marie-Tooth disease type 2 with prominent sensory dysfunction
Keywords: ارثی و نوروپاتی حسی; Charcot-Marie-Tooth; Hereditary motor and sensory neuropathy; MFN2; Mutation; Phenotype;
Sexual Functioning in Women with Mild and Severe Symptoms of Charcot-Marie-Tooth Disease
Keywords: ارثی و نوروپاتی حسی; Charcot-Marie-Tooth Disease; Female Sexuality; Hereditary Motor and Sensory Neuropathy
Pulmonary function in patients with hereditary motor and sensory neuropathy: A comparison of patients with and without spinal deformity
Keywords: ارثی و نوروپاتی حسی; Hereditary motor and sensory neuropathy; Charcot–Marie–Tooth disease; Spinal deformity; Respiratory muscle function; Static lung volume
Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot-Marie-Tooth type 2
Keywords: ارثی و نوروپاتی حسی; Charcot-Marie-Tooth disease; CMT2A; Hereditary motor and sensory neuropathy; MFN2; R104W mutation;
An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations
Keywords: ارثی و نوروپاتی حسی; 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
Hand involvement in children with Charcot–Marie-Tooth disease type 1A
Keywords: ارثی و نوروپاتی حسی; Peripheral neuropathy; Hereditary motor and sensory neuropathy; Charcot–Marie-Tooth disease; Paediatrics; Hand strength; Dynamometry
Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough
Keywords: ارثی و نوروپاتی حسی; Hereditary motor and sensory neuropathy; Proximal dominancy; HMSN-P; Cough; Elevated creatine kinase level; Neurogenic bladder
Factors that influence health-related quality of life in Australian adults with Charcot–Marie–Tooth disease
Keywords: ارثی و نوروپاتی حسی; Peripheral neuropathy; Charcot–Marie–Tooth disease; Hereditary motor and sensory neuropathy; Neuromuscular disease; Quality of life; Health Status; Predictive models; Questionnaire; Disability; Muscle weakness; Muscle cramp