Pages that link to "Q68296487"
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The following pages link to Prevalence and incidence of Becker muscular dystrophy (Q68296487):
Displaying 64 items.
- Becker muscular dystrophy (Q2484592) (← links)
- Prevention and treatment for cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy (Q24201115) (← links)
- Prevention and treatment for cardiac complications in Duchenne and Becker muscular dystrophy (Q24235432) (← links)
- Aminoglycosides and other nonsense suppression therapies for the treatment of dystrophinopathy (Q24240721) (← links)
- Cardiac involvement in Duchenne and Becker muscular dystrophy (Q26801616) (← links)
- Potential pseudoknots in the PrP-encoding mRNA (Q28205609) (← links)
- Identification of small molecule and genetic modulators of AON-induced dystrophin exon skipping by high-throughput screening (Q28472268) (← links)
- Investigation of a female manifesting Becker muscular dystrophy (Q33594351) (← links)
- Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups (Q33595755) (← links)
- Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis (Q33595768) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India. (Q33796134) (← links)
- Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies (Q33991470) (← links)
- Muscular dystrophies (Q34192076) (← links)
- Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients (Q34227098) (← links)
- Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association o (Q34386584) (← links)
- MLPA-based genotype-phenotype analysis in 1053 Chinese patients with DMD/BMD. (Q34604720) (← links)
- Comparative cost of illness analysis and assessment of health care burden of Duchenne and Becker muscular dystrophies in Germany (Q34998724) (← links)
- Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular Dystrophy (Q35055089) (← links)
- Recent advances in understanding muscular dystrophy (Q35534859) (← links)
- Exon deletion pattern in duchene muscular dystrophy in north west of iran (Q35576460) (← links)
- Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy (Q35582668) (← links)
- Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases (Q35625960) (← links)
- Prevalence of Duchenne and Becker muscular dystrophies in the United States (Q35770545) (← links)
- X-Linked Dilated Cardiomyopathy: A Cardiospecific Phenotype of Dystrophinopathy (Q35818371) (← links)
- Genetic and clinical correlations of Xp21 muscular dystrophy (Q35848767) (← links)
- Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations (Q36662506) (← links)
- Current understanding and management of dilated cardiomyopathy in Duchenne and Becker muscular dystrophy. (Q36949803) (← links)
- Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy (Q36953163) (← links)
- Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approach (Q36979169) (← links)
- Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online database (Q37109015) (← links)
- Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort (Q37591778) (← links)
- Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset (Q37632013) (← links)
- Becker muscular dystrophy-like myopathy regarded as so-called "fatty muscular dystrophy" in a pig: a case report and its diagnostic method. (Q37696517) (← links)
- In Utero Stem Cell Transplantation: Potential Therapeutic Application for Muscle Diseases. (Q39360944) (← links)
- Dystrophin, its gene, and the dystrophinopathies (Q40373239) (← links)
- Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy (Q41145047) (← links)
- DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathy (Q41740249) (← links)
- Duchenne/Becker muscular dystrophy: A report on clinical, biochemical, and genetic study in Gujarat population, India (Q41787397) (← links)
- Distribution of dystrophin gene deletions in a Chinese population (Q41844674) (← links)
- Growth hormone deficiency in a patient with becker muscular dystrophy: a pediatric case report. (Q41860729) (← links)
- Phenotype-genotype analysis of dystrophinopathy caused by duplication mutation in Dystrophin gene in an African patient (Q42014991) (← links)
- Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase (Q48006442) (← links)
- Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene. (Q51740291) (← links)
- Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study. (Q52862565) (← links)
- MLPA Application in Clinical Diagnosis of DMD/BMD in Shanghai. (Q54194415) (← links)
- Clinical Utility Gene Card for: Becker muscular dystrophy. (Q54269189) (← links)
- Molecular Analysis-Based Genetic Characterization of a Cohort of Patients with Duchenne and Becker Muscular Dystrophy in Eastern China. (Q55318559) (← links)
- DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients (Q57200516) (← links)
- Interventions for preventing and treating cardiac complications in Duchenne and Becker muscular dystrophy and X-linked dilated cardiomyopathy (Q57456679) (← links)
- Voltage-Dependent Sarcolemmal Ion Channel Abnormalities in the Dystrophin-Deficient Heart (Q58574774) (← links)
- Creation of a novel algorithm to identify patients with Becker and Duchenne muscular dystrophy within an administrative database and application of the algorithm to assess cardiovascular morbidity (Q64041140) (← links)
- Study of Dystrophinopathy in Eastern Uttar Pradesh Population of India. (Q64935011) (← links)
- Urine mRNA to identify a novel pseudoexon causing dystrophinopathy. (Q64963849) (← links)
- The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. I. Natural history (Q70569356) (← links)
- Dystrophinopathies (Q71509060) (← links)
- Becker muscular dystrophy presenting with complete heart block in the sixth decade (Q71749013) (← links)
- Abnormal dystrophin expression in patients with limb girdle syndromes (Q72470505) (← links)
- Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation (Q78190267) (← links)
- Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of them (Q84934413) (← links)
- [Specific features of Becker Muscular Dystrophy patients and female carriers of Duchenne Muscular Dystrophy] (Q87092279) (← links)
- New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy (Q87373932) (← links)
- Natural history of cardiac function in Duchenne and Becker muscular dystrophies on home mechanical ventilation (Q89444366) (← links)
- Hereditary muscle diseases and the heart: the cardiologist's perspective (Q96304353) (← links)