Keywords: میوپاتی Centronuclear; Neuromuscular disorders; Congenital myopathies; Genetics; Therapy; CCD; Central Core Disease; CFTD; Congenital Fibre Type Disproportion; CNM; Centronuclear Myopathy; MmD; Multi-minicore Disease; NM; Nemaline Myopathy;
مقالات ISI میوپاتی Centronuclear (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: میوپاتی Centronuclear; Congenital muscular dystrophy; Congenital myopathy; Ullrich congenital muscular dystrophy; Nemaline myopathy; Central core myopathy; Centronuclear myopathy; Merosin deficiency congenital muscular dystrophy;
Keywords: میوپاتی Centronuclear; Necklace fibres; MTM1; DNM2; Centronuclear myopathy; 3D electron microscopy;
An integrated modelling methodology for estimating the prevalence of centronuclear myopathy
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Causative gene; Severity; Incidence; Prevalence; Geographic region;
Case reportGrand paternal inheritance of X-linked myotubular myopathy due to mosaicism, and identification of necklace fibers in an asymptomatic male
Keywords: میوپاتی Centronuclear; Myotubular myopathy; Centronuclear myopathy; Myotubularin 1; MTM1; X-linked; Paternal transmission; Necklace fiber;
Insights from genotype-phenotype correlations by novel SPEG mutations causing centronuclear myopathy
Keywords: میوپاتی Centronuclear; SPEG; Exome; Centronuclear myopathy; Myotubular myopathy; Whole body MRI;
Pathophysiological consequences of receptor mistraffic: Tales from the platelet P2Y12 receptor
Keywords: میوپاتی Centronuclear; ADP; Adenosine diphosphate; CNM; centronuclear myopathy; CMT; Charcot-Marie- Tooth; CAMs; constitutively active mutants; GAPP; Genotyping and Phenotyping of Platelets consortium; GPCR; G protein-coupled receptor; GRK; G protein-coupled receptor kinase
Ca2+ handling abnormalities in early-onset muscle diseases: Novel concepts and perspectives
Keywords: میوپاتی Centronuclear; Cav1.1; alfa 1 subunit of the dihydropyridine receptor; CCD; central core disease; CNM; centronuclear myopathy; DHPR; dihydropyridine receptor; ECC; excitation contraction coupling; ECCE; excitation coupled calcium entry; ER; endoplasmic reticulum; HDAC;
WANTED - Dead or alive: Myotubularins, a large disease-associated protein family
Keywords: میوپاتی Centronuclear; Congenital myopathy; Neuropathy; GTEx database; Sbf1; Myotubular myopathy; Myotubularin; MTM; Myotubularins; PPIn; phosphoinositides; PtdIns; phosphatidylinositol; CNM; centronuclear myopathy; CMT; Charcot-Marie-Tooth neuropathy; PH-GRAM; Pleckstrin Homol
Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients
Keywords: میوپاتی Centronuclear; RYR1; Centronuclear myopathy; Congenital myopathies;
A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels
Keywords: میوپاتی Centronuclear; centronuclear myopathy; myotubular myopathy; MTM1; myotubularin; congenital myopathy;
A novel dynamin-2 gene mutation associated with a late-onset centronuclear myopathy with necklace fibres
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Dynamin 2; Necklace fibre;
A novel mutation in the DNM2 gene impairs dynamin 2 localization in skeletal muscle of a patient with late onset centronuclear myopathy
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Muscle biopsy; DNM2 gene; Dynamin; Myosin VI; Dystrophin;
Adult centronuclear myopathies: A hospital-based study
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; DNM2; BIN1; MTM1; Myotubular myopathy; Myopathie centronucléaire; DNM2; BIN1; MTM1; Myopathie myotubulaire;
Clinicopathological features of centronuclear myopathy in Japanese populations harboring mutations in dynamin 2
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Dynamin 2; Congenital myopathy; Radial distribution; Clinicopathological homology
Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutation
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Myotubularin; MTM1; X-linked recessive myotubular myopathy; Manifesting carriers; Necklace fibers
182nd ENMC International Workshop: RYR1-related myopathies, 15-17th April 2011, Naarden, The Netherlands
Keywords: میوپاتی Centronuclear; CCD; Central Core Disease; CNM; Centronuclear Myopathy; E-C; excitation-contraction; MH; malignant hyperthermia; MHS; malignant hyperthermia susceptibility; MmD; Multi-minicore Disease; RYR1; skeletal muscle ryanodine receptor gene; RyR1; skeletal mus
Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies
Keywords: میوپاتی Centronuclear; Congenital myasthenic syndromes; Centronuclear myopathy; Neuromuscular junction; Acetylcholinesterase inhibitors
Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Neuromuscular junction; Myasthenic syndrome; Synaptic vesicle cycle
Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset
Keywords: میوپاتی Centronuclear; DNM2; Dynamin 2; Pleckstrin homology; GTPase; Mutation; Congenital myopathy; Centronuclear myopathy; Myotubular myopathy; Charcot-Marie-Tooth neuropathy; Myotubularin; Amphiphysin; RYR1; Neonatal
Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutation
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; DNM2; Dynamin 2; Muscle hypertrophy; Muscle pseudohypertrophy; Necklace fibers; Neutropenia
Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Myotubular myopathy; Myotubularin; Intronic mutations; MTM1; XLMTM;
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy
Keywords: میوپاتی Centronuclear; DNM2; Centronuclear myopathy; Whole body MRI; Dynamin; Muscular dystrophy
What’s new in congenital myopathies?
Keywords: میوپاتی Centronuclear; Congenital myopathy; Nemaline myopathy; Central core disease; Centronuclear myopathy; Congenital fibre type disproportion
Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Dynamin 2; Mental retardation; DNM2-DI-CMTB;
MRI in DNM2-related centronuclear myopathy: Evidence for highly selective muscle involvement
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Dynamin 2; MRI;
Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Morphometry; MTM1; Myotubularin; X-linked myotubular myopathy
Immunocytochemical study of cytoskeletal proteins in centronuclear myopathies
Keywords: میوپاتی Centronuclear; Centronuclear myopathy; Myotubular myopathy; Immunocytochemistry; Vimentin; Desmin; Dystrophin