about
Next-generation sequencing identifies transportin 3 as the causative gene for LGMD1FRole of Radiologic Imaging in Genetic and Acquired Neuromuscular DisordersUpdate in inclusion body myositisChemical shift-based MRI to measure fat fractions in dystrophic skeletal muscle.Quantitative proton MR techniques for measuring fatSkeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patientsMuscle imaging data in late-onset Pompe disease reveal a correlation between the pre-existing degree of lipomatous muscle alterations and the efficacy of long-term enzyme replacement therapy.Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).Reproducibility, and age, body-weight and gender dependency of candidate skeletal muscle MRI outcome measures in healthy volunteers.Upper girdle imaging in facioscapulohumeral muscular dystrophy.Comparison of clinical semi-quantitative assessment of muscle fat infiltration with quantitative assessment using chemical shift-based water/fat separation in MR studies of the calf of post-menopausal women.Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing lossDifferent molecular signatures in magnetic resonance imaging-staged facioscapulohumeral muscular dystrophy muscles.A combined laser microdissection and mass spectrometry approach reveals new disease relevant proteins accumulating in aggregates of filaminopathy patientsOngoing developments in sporadic inclusion body myositisSporadic inclusion body myositis: new insights and potential therapy.Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis.Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol.Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy: mdx, Largemyd and mdx/Largemyd.Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies.Muscle MR imaging in tubular aggregate myopathyLimb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern.Magnetic Resonance Assessment of Hypertrophic and Pseudo-Hypertrophic Changes in Lower Leg Muscles of Boys with Duchenne Muscular Dystrophy and Their Relationship to Functional Measurements.Whole-body magnetic resonance imaging evaluation of facioscapulohumeral muscular dystrophyTitin mutation segregates with hereditary myopathy with early respiratory failure.Congenital myopathy caused by a novel missense mutation in the CFL2 gene.Measurement of intramuscular fat by muscle echo intensity.Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia.Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.Extra-ocular muscle MRI in genetically-defined mitochondrial diseaseMuscle MRI in muscular dystrophiesImaging alterations in skeletal muscle channelopathies: a study in 15 patientsBioimpedance Analysis as a Method to Evaluate the Proportion of Fatty and Muscle Tissues in Progressive Myopathy in Pompe DiseaseMuscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotonias.Multicenter prospective longitudinal study of magnetic resonance biomarkers in a large duchenne muscular dystrophy cohort."Target" and "Sandwich" Signs in Thigh Muscles have High Diagnostic Values for Collagen VI-related Myopathies.Muscle magnetic resonance imaging in congenital myasthenic syndromes.Whole-body MRI for full assessment and characterization of diffuse inflammatory myopathy.Distinct disease phases in muscles of facioscapulohumeral dystrophy patients identified by MR detected fat infiltrationIntermuscular fat: a review of the consequences and causes
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Neuromuscular imaging in inherited muscle diseases
@ast
Neuromuscular imaging in inherited muscle diseases
@en
Neuromuscular imaging in inherited muscle diseases
@nl
type
label
Neuromuscular imaging in inherited muscle diseases
@ast
Neuromuscular imaging in inherited muscle diseases
@en
Neuromuscular imaging in inherited muscle diseases
@nl
prefLabel
Neuromuscular imaging in inherited muscle diseases
@ast
Neuromuscular imaging in inherited muscle diseases
@en
Neuromuscular imaging in inherited muscle diseases
@nl
P2093
P2860
P1433
P1476
Neuromuscular imaging in inherited muscle diseases
@en
P2093
Dirk Fischer
Mike P Wattjes
Rudolf A Kley
P2860
P2888
P304
P356
10.1007/S00330-010-1799-2
P407
P577
2010-04-27T00:00:00Z
2010-10-01T00:00:00Z