Pages that link to "Q77924716"
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The following pages link to Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study (Q77924716):
Displaying 50 items.
- Cardiac involvement in Duchenne and Becker muscular dystrophy (Q26801616) (← links)
- Clinical and genetic characterization of manifesting carriers of DMD mutations (Q34151973) (← links)
- How calcium influx through calcium leak channels is responsible for the elevated levels of calcium-dependent proteolysis in dystrophic myotubes (Q34204770) (← links)
- Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype (Q34380291) (← links)
- Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy (Q34474581) (← links)
- Functional performance and muscle strength phenotypes in men and women with Danon disease (Q34680781) (← links)
- Carrier woman of Duchenne muscular dystrophy mimicking inflammatory myositis (Q34753555) (← links)
- Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathy (Q35164387) (← links)
- The correlation analysis of functional factors and age with duchenne muscular dystrophy (Q35843560) (← links)
- Clinical and Genetic Characterization of Female Dystrophinopathy (Q35866121) (← links)
- Utility of MLPA in mutation analysis and carrier detection for Duchenne muscular dystrophy (Q36064194) (← links)
- Genome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophy (Q36109634) (← links)
- MRI/MRS evaluation of a female carrier of Duchenne muscular dystrophy (Q36279798) (← links)
- Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy (Q36380483) (← links)
- Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. (Q36422465) (← links)
- Progress in gene therapy of dystrophic heart disease (Q36773242) (← links)
- Diagnostic utility of cardiac magnetic resonance for detection of cardiac involvement in female carriers of Duchenne muscular dystrophy (Q36982543) (← links)
- Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita. (Q37014569) (← links)
- Cardiac involvement in Becker muscular dystrophy (Q37098320) (← links)
- Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever Model (Q37148808) (← links)
- Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers (Q37278457) (← links)
- Muscular dystrophy therapy by nonautologous mesenchymal stem cells: muscle regeneration without immunosuppression and inflammation (Q37352442) (← links)
- Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency (Q37375715) (← links)
- Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports (Q37591031) (← links)
- Review of Duchenne Muscular Dystrophy (DMD) for the Pediatricians in the Community (Q37781212) (← links)
- Sex differences in cardiomyopathies (Q38182007) (← links)
- Costamere proteins and their involvement in myopathic processes. (Q38531654) (← links)
- Knowledge of carrier status and barriers to testing among mothers of sons with Duchenne or Becker muscular dystrophy (Q38793510) (← links)
- Cardiac pathologies in female carriers of Duchenne muscular dystrophy assessed by cardiovascular magnetic resonance imaging (Q41190888) (← links)
- A De novo Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient (Q42267389) (← links)
- Risk of fracture in patients with muscular dystrophies (Q44704141) (← links)
- Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency (Q46237286) (← links)
- Clinical and genetic characterisation of dystrophin-deficient muscular dystrophy in a family of Miniature Poodle dogs. (Q50422172) (← links)
- Low dystrophin levels in heart can delay heart failure in mdx mice. (Q51164233) (← links)
- A retrospective analysis of 237 Chinese families with Duchenne muscular dystrophy history and strategies of prenatal diagnosis. (Q52336125) (← links)
- Manifesting carriage of a Duchenne muscular dystrophy mutation: an unusual cause of impaired lung function in CF. (Q54487655) (← links)
- Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl. (Q55217300) (← links)
- On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers (Q58052179) (← links)
- Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan (Q59876124) (← links)
- Identification of Cardiomyopathy-Associated Circulating miRNA Biomarkers in Muscular Dystrophy Female Carriers Using a Complementary Cardiac Imaging and Plasma Profiling Approach (Q60938968) (← links)
- Voluntary exercise improves muscle function and does not exacerbate muscle and heart pathology in aged Duchenne muscular dystrophy mice (Q63301935) (← links)
- Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients (Q64249045) (← links)
- Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy (Q73226910) (← links)
- Cardiomyopathy in a carrier of Duchenne's muscular dystrophy (Q74185698) (← links)
- Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia (Q81258363) (← links)
- Duchenne Muscular Dystrophy: a Survey of Perspectives on Carrier Testing and Communication Within the Family (Q86517065) (← links)
- [Specific features of Becker Muscular Dystrophy patients and female carriers of Duchenne Muscular Dystrophy] (Q87092279) (← links)
- [Cardiac involvement in dystrophinopathies] (Q87092283) (← links)
- Predicting gait adaptations due to ankle plantarflexor muscle weakness and contracture using physics-based musculoskeletal simulations (Q90561522) (← links)
- Novel mosaic mutation in the dystrophin gene causing distal asymmetric muscle weakness of the upper limbs and dilated cardiomyopathy (Q90602378) (← links)