Results 121 to 130 of about 6,773 (176)

A retrospective cohort study and review of the literature about germline mosaicism in Duchenne/Becker muscular dystrophy prenatal counseling: How to estimate the recurrence risk in clinical settings? [PDF]

J Genet Couns
Verebi C, Gravrand V, Bienvenu T, Leturcq F, Nectoux J.   +4 more
europepmc   +1 more source

Caregiver Burden with Duchenne and Becker Muscular Dystrophy in Japan: A Clinical Observation Study. [PDF]

Intern Med
Ishizaki M, Kobayashi M, Hashimoto H, Nakamura A, Maeda Y, Ueyama H, Matsumura T.   +6 more
europepmc   +1 more source

Imaging mass cytometry analysis of Becker muscular dystrophy muscle samples reveals different stages of muscle degeneration. [PDF]

Sci Rep
Piñol-Jurado P, Verdú-Díaz J, Fernández-Simón E, Domínguez-González C, Hernández-Lain A, Lawless C, Vincent A, González-Chamorro A, Villalobos E, Monceau A, Laidler Z, Mehra P, Clark J, Filby A, McDonald D, Rushton P, Bowey A, Alonso Pérez J, Tasca G, Marini-Bettolo C, Guglieri M, Straub V, Suárez-Calvet X, Díaz-Manera J.   +23 more
europepmc   +1 more source

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Evaluation of the cardiomyopathy in becker muscular dystrophy

Muscle and Nerve, 1995
AbstractTo evaluate the features and the course of cardiomyopathy in Becker muscular dystrophy, 68 patients–identified by clinical assessment and by reduced dystrophin labeling and/or DNA analysis–were followed in the years 1976–1993, for periods ranging from 3 to 18 years (mean 8).
Giovanni Nigro, , Vincenzo Nigro
exaly   +5 more sources

Becker‐type muscular dystrophy

Muscle & Nerve, 1978
AbstractThis is a review of clinical, cardiologic, electrophysiologic, pathologic, and serum creatine kinase changes in eight families with slowly progressive X‐linked Becker‐type muscular dystrophy. All but one of the patients were able to walk until the age of 16 years, and most lived beyond 20.
W G, Bradley, M Z, Jones, J M, Mussini, P R, Fawcett   +3 more
openaire   +2 more sources

Muscular Dystrophy in a Dog Resembling Human Becker Muscular Dystrophy

Journal of Comparative Pathology, 2014
A 3-year-old, male Labrador retriever dog was presented with clinical signs of progressive exercise intolerance, bilateral elbow extension, rigidity of the forelimbs, hindlimb flexion and kyphosis. Microscopical examination of muscle tissue showed marked variability in myofibre size, replacement of muscle with mature adipose tissue and degeneration ...
Baroncelli AB, Abellonio F, Pagano TB, Esposito I, Peirone B, PAPPARELLA, SERENELLA, PACIELLO, ORLANDO   +6 more
openaire   +3 more sources

[Becker muscular dystrophy].

Ryoikibetsu shokogun shirizu, 2001
Abstract Becker strongly believed that the newly discovered muscular dystrophy was allelic to DMD. For many years Duchenne type and Becker type of muscular dystrophy were considered to be distinct genetic entities. In 1983, Kingston et al.
Marianne de Visser, Edo M Hoogerwaard
openaire   +3 more sources

Prevalence and incidence of Becker muscular dystrophy

Lancet, The, 1991
We measured the prevalence and incidence of Becker muscular dystrophy in the Northern Health Region of England, UK. Patients were identified from the records of the Regional Neurological Centre and Muscular Dystrophy Group laboratories, Newcastle upon Tyne, and by writing to local doctors. We used cDNA probes and/or dystrophin immunolabelling of muscle-
K M Bushby, D Gardner-Medwin
exaly   +3 more sources