Keywords: Isoprostanes; Aging; Exercise; Training; ROS; reactive-oxygen species; IsoP; Isoprostane; VËO2max; Maximal oxygen uptake; MAP; Maximal aerobic power; Lamax; Venous blood-lactate concentration at VËO2max; La30; Venous blood-lactate concentration at 30Â m
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: Factor analysis; Neuromuscular diseases; Outcome measure; Psychometrics; CMT; Charcot-Marie-Tooth disease; CFA; confirmatory factor analysis; D1; standing position and transfers; D2; axial and proximal motor function; D3; distal motor function; DM1; myoto
Keywords: Facioscapulohumeral muscular dystrophy; FSHD; D4Z4 macrosatellites; Southern blot; Anticipation;
Keywords: FSHD; DUX4; D4Z4; Disease model; Epigenetic; DNA methylation;
Keywords: MRI; Hyperintensity quantification; Muscle dystrophy; Muscle-region segmentation; FSHD
Keywords: Balance; Postural control; Neuromuscular disorders; FSHD
Keywords: CALQ1; calsequestrin-1; Cav-3; caveolin-3; DHPR; dihydropyridine receptor; DMD; Duchenne muscular dystrophy; DYNC1LI2; cytoplasmic dynein 1 light intermediate chain 2; FLIM-FRET; fluorescence lifetime imaging-fluorescence resonance energy transfer; FS
Telemedicine for Facio-Scapulo-Humeral Muscular Dystrophy: A multidisciplinary approach to improve quality of life and reduce hospitalization rate?
Keywords: Telemedicine; FSHD; Telerehabilitation; Neuromuscular disorders; Repisratory failure; Multidisciplinary approach;
Perturbation of muscle metabolism in patients with muscular dystrophy in early or acute phase of disease: In vitro, high resolution NMR spectroscopy based analysis
Keywords: BCA; branched chain amino acids; Lac; lactate; Gln/glu; glutamine/glutamate; Ala; alanine; Ace; acetate; Suc; succinate; Cr/PCr; creatine/phosphocreatine; GPC/Car; glycerophosphocholine/ carnitine; Fum; fumarate; His; histidine; Tyr; tyrosine; Prop; propi
Abnormal lipid metabolism in skeletal muscle tissue of patients with muscular dystrophy: In vitro, high-resolution NMR spectroscopy based observation in early phase of the disease
Keywords: DMD; Duchenne muscular dystrophy; BMD; Becker muscular dystrophy; FSHD; Facioscapulohumeral muscular dystrophy; LGMD-2B; Limb girdle muscular dystrophy-2B; TG; Triglycerides; PL; Phospholipids; CHOL; Total cholesterol; TSP; [3-(trimethylsilyl) propionic-2
International meeting of the French society of neurology 2016Muscle MRI of facioscapulohumeral dystrophy (FSHD): A growing demand and a promising approach
Keywords: MRI; Facioscapulohumeral dystrophy; FSHD; Measurement; Pattern recognition;
A cross sectional study of two independent cohorts identifies serum biomarkers for facioscapulohumeral muscular dystrophy (FSHD)
Keywords: FSHD; Facioscapulohumeral; D4Z4; DUX4; Biomarker; Proteomics; Muscular dystrophy; Creatine kinase; Carbonic anhydrase; Troponin;
Metabolic status of patients with muscular dystrophy in early phase of the disease: In vitro, high resolution NMR spectroscopy based metabolomics analysis of serum
Keywords: Metabolites; Muscular dystrophy; DMD; BMD; FSHD; LGMD; DM; Blood; Serum;
Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy
Keywords: Respiratory failure; Facioscapulohumeral muscular dystrophy; Pulmonary function tests; Mechanical ventilation; Neuromuscular respiratory dysfunction; AHI; apnea/hypopnea index; BMI; body mass index; ERV; expiratory reserve volume; FSHD; facioscapulohumera
Dux4 induces cell cycle arrest at G1 phase through upregulation of p21 expression
Keywords: FSHD; Dux4; p21; Cell cycle;
Skeletal muscle imaging in facioscapulohumeral muscular dystrophy, pattern and asymmetry of individual muscle involvement
Keywords: Fatty infiltration; FSHD; Muscle imaging; Neuromuscular disorders; Computer tomography;
Myotonic dystrophy type 1 and de novo FSHD mutation double trouble: A clinical and muscle MRI study
Keywords: Myotonic dystrophy type 1; FSHD; Double trouble; Muscle MRI study;
Muscular Dystrophies and Other Genetic Myopathies
Keywords: Muscular dystrophy; Myopathy; Limb-Girdle; FSHD; Myotonic dystrophy; Congenital; Metabolic;
Value of muscle enzyme measurement in evaluating different neuromuscular diseases
Keywords: DMD/BMD; Duchene/Becker muscular dystrophy; FSHD; facioscapulohumeral muscular dystrophy; LGMD; limb-girdle muscular dystrophy; PM; polymyositis; LSM; lipid storage myopathy; MND; motor neuron disease; SMA; spinal muscular atrophy; Muscle enzymes; Neuromu
Compound heterozygosity in a South African patient with Facioscapulohumeral muscular dystrophy
Keywords: Facioscapulohumeral muscular dystrophy; FSHD; Compound heterozygote; Muscular dystrophy; Genotype-phenotype correlation;
Evolutionary history of linked D4Z4 and Beta satellite clusters at the FSHD locus (4q35)
Keywords: Primate evolution; Chimpanzee; Beta satellite; D4Z4; 4q35; FSHD;
Case studyEpilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy
Keywords: Epilepsy; Partial seizures; Psychomotor retardation; FSHD; Muscular dystrophy;
Control of the upper body movements during level walking in patients with facioscapulohumeral dystrophy
Keywords: Gait; Head stability; Accelerations; FSHD; Muscular disorders
Neuromuscular Electrical Stimulation Training: A Safe and Effective Treatment for Facioscapulohumeral Muscular Dystrophy Patients
Keywords: Isometric contraction; Quadriceps muscle; Rehabilitation; Shoulder; CK; creatine kinase; ES; effect size; FSHD; facioscapulohumeral muscular dystrophy; MMT; manual muscle test; MVIC; maximal voluntary isometric contraction; 6MWT; six-minute walk test; NME
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy
Keywords: MR imaging; Neuromuscular disease; FSHD
Novel mitochondrial tRNALeu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype
Keywords: mtDNA; Mitochondrial myopathy; FSHD;
Facioscapulohumeral Muscular Dystrophy
Keywords: FSHD; facioscapulohumeral muscular dystrophy; muscular dystrophy; myostatin; chromosome 4;
Epigenetic mechanisms of facioscapulohumeral muscular dystrophy
Keywords: FSHD; Muscular dystrophy; D4Z4 repeat; Epigenetics; Chromatin; Nuclear organization
Facioscapulohumeral muscular dystrophy
Keywords: FSHD; Muscular dystrophy; Review; D4Z4; Therapy; Epigenetic
The development of a model of fatigue in neuromuscular disorders: A longitudinal study
Keywords: Fatigue; Longitudinal; FSHD; Adult-onset MD; HMSN-I
RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA
Keywords: FSHD; Transcription analysis; Gene expression; Chromatin immunoprecipitation; Satellite DNA; DNA repeat array
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
Keywords: FSHD; Muscle; DUX4; Homeobox; Apoptosis
The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B
Keywords: Facioscapulohumeral muscular dystrophy; FSHD; D4Z4;
Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy
Keywords: FSHD; Facioscapulohumeral muscular dystrophy; D4Z4; Mosaicism; Non-penetrance;