Abstract
References
Articles referenced by this article (35)
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies.
Neurology, (4):465-474 1989
MED: 2927671
Clinical investigation in Duchenne dystrophy: 2. Determination of the "power" of therapeutic trials based on the natural history.
Muscle Nerve, (2):91-103 1983
MED: 6343858
Distinct dystrophin mRNA species are expressed in embryonic and adult mouse skeletal muscle.
FEBS Lett, (1):47-52 1988
MED: 3060377
Duchenne muscular dystrophy
1987
Clinical studies in benign (Becker type) X-linked muscular dystrophy.
Clin Genet, (4):189-201 1976
MED: 975594
Duchenne dystrophy
1986
Clinical trials in Duchenne dystrophy. Standardization and reliability of evaluation procedures.
Phys Ther, (1):41-45 1984
MED: 6361809
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.
Genomics, (2):109-114 1988
MED: 3410474
The clinical examination of the voluntary muscles
1974
Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
Cell, (6):919-928 1987
MED: 3319190
Show 10 more references (10 of 35)
Citations & impact
Impact metrics
Article citations
Personalized and muscle-specific OXPHOS measurement with integrated CrCEST MRI and proton MR spectroscopy.
Nat Commun, 15(1):5387, 25 Jun 2024
Cited by: 1 article | PMID: 38918361 | PMCID: PMC11199598
Age-Related Blood Levels of Creatine Kinase-MM in Newborns and Patients with Duchenne Muscular Dystrophy: Considerations for the Development of Newborn Screening Algorithms.
Int J Neonatal Screen, 10(2):41, 19 Jun 2024
Cited by: 0 articles | PMID: 38920848 | PMCID: PMC11203585
Semaphorins: Missing Signals in Age-dependent Alteration of Neuromuscular Junctions and Skeletal Muscle Regeneration.
Aging Dis, 15(2):517-534, 01 Apr 2024
Cited by: 1 article | PMID: 37728580 | PMCID: PMC10917540
Review Free full text in Europe PMC
Brothers with Becker muscular dystrophy show discordance in skeletal muscle computed tomography findings: A case report.
SAGE Open Med Case Rep, 12:2050313X231221436, 03 Jan 2024
Cited by: 0 articles | PMID: 38187815 | PMCID: PMC10768573
MicroRNAs as a Tool for Differential Diagnosis of Neuromuscular Disorders.
Neuromolecular Med, 25(4):603-615, 19 Oct 2023
Cited by: 0 articles | PMID: 37856057 | PMCID: PMC10721695
Go to all (82) article citations
Similar Articles
To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation.
Evaluation of carrier detection rates for Duchenne and Becker muscular dystrophies using serum creatine-kinase (CK) and pyruvate-kinase (PK) through discriminant analysis.
Am J Med Genet, 25(2):219-230, 01 Oct 1986
Cited by: 6 articles | PMID: 3777019
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.
Am J Med Genet, 80(4):356-361, 01 Dec 1998
Cited by: 21 articles | PMID: 9856563
Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophies.
Hum Hered, 41(6):370-378, 01 Jan 1991
Cited by: 0 articles | PMID: 1797630
Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.
Hum Genet, 66(1):17-40, 01 Jan 1984
Cited by: 258 articles | PMID: 6365739
Review