[Use of DNA analysis in the prevention of progressive muscular dystrophies].
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DNA Probes↗
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Results for “PROGRESSIVE MUSCULAR DYSTROPHY”
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[Ultrastructural study of progressive muscular dystrophy].
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Adolescent↗
[Establishment of systemic dental health services for Duchenne-type progressive muscular dystrophy patients].
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Activities of Daily Living↗
[A study on the pronunciation in patients with progressive muscular dystrophy (author's transl)].
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Humans↗
[Orodental aspects in patients with progressive muscular dystrophy].
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Adolescent↗
[Na, K+-ATP-ase activity of erythrocyte membranes in progressive muscular dystrophy].
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Adolescent↗
Na+ + K+ ATPase of erythrocyte membrane in progressive muscular dystrophy.
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Adolescent↗
[Clinical polymorphism and genetic heterogeneity in Duchenne's progressive muscular dystrophy in girls (a review)].
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Adult↗
[Molecular cytogenetics of progressive muscular dystrophy].
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Genes↗
[Progressive muscular dystrophy in a child with a symptomatic carrier mother].
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Adult↗
[Progressive muscular dystrophy: CPK, LDH, ALD (aldolase)--EMG, ECG in patients and their families].
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Creatine Kinase↗
[Plasma level of hemopexin (Hpx) in families with progressive muscular dystrophy (PMD)].
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Creatine Kinase↗
[A combination of Duchenne's progressive muscular dystrophy with congenital ichthyosis--a deletion or 2 independent gene mutations at Xp21--Xp22?].
The authors describe a combination of Duchenne muscular dystrophy and congenital ichthyosis in a 6.5-year-old boy. This is the first ever description appearing in the world literature. The authors discuss possible variants of mutation (either chromosomal aberration or two independent gene mutations in chromosome 21).
Child↗
[Clinical and pathologic analysis of progressive muscular dystrophy].
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Adolescent↗
[Pseudohypertrophic progressive muscular dystrophy with a malignant course in young girls].
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Adolescent↗
[Immunoglobulin, complement and hemopexin in patients with progressive muscular dystrophy and in their parents].
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Adult↗
[Use of expert systems in the clinical genetics of polydactyly and progressive muscular dystrophies].
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Abnormalities, Multiple↗
Biochemical changes in hereditary progressive muscular dystrophies. Defect of protein synthesis in fibroblasts, muscle tissues and blood cells.
80S ribosomes and ribosomal subunits were isolated from fibroblasts, muscle tissues and blood cells of patients with different muscular dystrophies (MD) as well as of controls and were used for in vitro measurement of ribosomal protein synthesis (RPS) in a poly(U)-directed polyphenylalanine synthesis system. The activity of ribosomes from the patients showed a disease-dependent decrease compared to normal controls. Examination of hybrid 80S ribosomes consisting of 40S and 60S subunits of patients and the corresponding control cells revealed that the loss of RPS activity was related to one or both of the ribosomal subunits depending on the type of MD.
Blood Cells↗