Pages that link to "Q45278547"
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The following pages link to The frequency of limb girdle muscular dystrophy 2A in northeastern Italy (Q45278547):
Displaying 30 items.
- Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review). (Q33608787) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Limb-girdle Muscular Dystrophies in India: A Review (Q33795491) (← links)
- Limb-girdle muscular dystrophy subtypes: First-reported cohort from northeastern China (Q34094843) (← links)
- Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India. (Q36134506) (← links)
- Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation. (Q36254120) (← links)
- Impaired regeneration in LGMD2A supported by increased PAX7-positive satellite cell content and muscle-specific microrna dysregulation (Q36791425) (← links)
- Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations. (Q37004486) (← links)
- Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance (Q37039715) (← links)
- Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle (Q37295056) (← links)
- Epidemiology of muscular dystrophies in the Mediterranean area (Q37735439) (← links)
- Molecular diagnosis of muscular dystrophies, focused on limb girdle muscular dystrophies (Q38089840) (← links)
- Genetic basis of limb-girdle muscular dystrophies: the 2014 update (Q38213016) (← links)
- Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: The yield and the pitfalls (Q38434135) (← links)
- The Growing Family of Limb-Girdle Muscular Dystrophies: Old and Newly Identified Members (Q38528085) (← links)
- A Systematic Review and Meta-analysis on the Epidemiology of the Muscular Dystrophies (Q38703274) (← links)
- Limb-girdle muscular dystrophies - international collaborations for translational research (Q38795106) (← links)
- Limb-girdle muscular dystrophy in the Agarwals: Utility of founder mutations in CAPN3 gene (Q38839318) (← links)
- Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A. (Q41110857) (← links)
- Treadmill Training with HAL Exoskeleton-A Novel Approach for Symptomatic Therapy in Patients with Limb-Girdle Muscular Dystrophy-Preliminary Study (Q41334112) (← links)
- Molecular Diagnosis of Limb-girdle Muscular Dystrophy Type 2A by Next-generation Sequencing. (Q42203939) (← links)
- How to tackle the diagnosis of limb-girdle muscular dystrophy 2A (Q42271189) (← links)
- A large deletion and novel point mutations in the calpain 3 gene (CAPN3) in Bulgarian LGMD2A patients (Q43928606) (← links)
- The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B). (Q44350367) (← links)
- cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark (Q50547039) (← links)
- Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients (Q61943899) (← links)
- Estimating prevalence for limb-girdle muscular dystrophy based on public sequencing databases (Q64039277) (← links)
- Muscular dystrophies (Q86291937) (← links)
- European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) (Q90296161) (← links)
- Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia (Q91589129) (← links)