Pages that link to "Q73739715"
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The following pages link to The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach (Q73739715):
Displaying 30 items.
- Immunohistochemical analysis of calpain 3: advantages and limitations in diagnosing LGMD2A (Q24339386) (← links)
- Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy (Q28083989) (← links)
- Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2A (Q33578177) (← links)
- Genetic diseases of muscle (Q34997853) (← links)
- The 10 autosomal recessive limb-girdle muscular dystrophies (Q35201105) (← links)
- Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression. (Q35843389) (← links)
- Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations (Q36418689) (← links)
- Respiratory involvement in inherited primary muscle conditions (Q36596271) (← links)
- Natural history of LGMD2A for delineating outcome measures in clinical trials (Q36759458) (← links)
- Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations. (Q37004486) (← links)
- Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies (Q37329558) (← links)
- Molecular diagnosis in LGMD2A: mutation analysis or protein testing? (Q40500450) (← links)
- Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A. (Q41110857) (← links)
- Characteristic Posterior-dominant Lower Limb Muscle Involvement in Limb-girdle Muscular Dystrophy due to a DNAJB6 Phe93Leu Mutation (Q42264761) (← links)
- How to tackle the diagnosis of limb-girdle muscular dystrophy 2A (Q42271189) (← links)
- CAPN3 mRNA processing alteration caused by splicing mutation associated with novel genomic rearrangement of Alu elements (Q42628242) (← links)
- The phenotype of limb-girdle muscular dystrophy type 2I (Q44411539) (← links)
- Clinical variability in calpainopathy: what makes the difference? (Q46368478) (← links)
- Postmortem changes in myofibrillar-bound calpain 3 revealed by immunofluorescence microscopy (Q47747299) (← links)
- cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark (Q50547039) (← links)
- 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th-9th June 2002, Naarden, the Netherlands. (Q53304609) (← links)
- Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs (Q57390205) (← links)
- Genome-Wide Association Studies Based on Equine Joint Angle Measurements Reveal New QTL Affecting the Conformation of Horses. (Q64981242) (← links)
- Myopathies with early contractures (Q82029853) (← links)
- Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2 : a whole body highfield MRI study (Q82703390) (← links)
- MRI in the assessment of muscular pathology: a comparison between limb-girdle muscular dystrophies, hyaline body myopathies and myotonic dystrophies (Q83006075) (← links)
- A novel CAPN3 mutation in late-onset limb-girdle muscular dystrophy with early respiratory insufficiency (Q88444942) (← links)
- Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia (Q91589129) (← links)
- Facio-scapulo-humeral muscular dystrophy with early joint contractures and rigid spine (Q91911072) (← links)
- Calpainopathy: Description of a Novel Mutation and Clinical Presentation with Early Severe Contractures (Q93006406) (← links)