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Electrophysiological evaluation in myotonic dystrophy - Correlation with CTG length expansion
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 2001)
Immunophenotyping lymphocyte and acute phase proteins in canine x-linked muscular dystrophy
(2018-07-01)
Duchenne Muscular Dystrophy (DMD) is the most common X-linked muscular disease affecting humans. The Golden Retriever Muscular Dystrophy model (GRMD) is consider the most suitable for several studies. This assay aims to ...
Hand Function in Muscular Dystrophies: Relationship Between Performance of Upper Limb and Jebsen-Taylor Tests
(Sage Publications Inc, 2017)
The aim of this study was to investigate the relationship between Performance of Upper Limb (PUL) and Jebsen-Taylor Test (JTT) to assess and monitor upper limb function progression in patients with muscular dystrophy. ...
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
(BMJ Publishing Group, 2019)
© Author(s) (or their employer(s)) 2019.Background and objective Oculopharyngeal muscular dystrophy (OPMD) is a genetic disorder caused by an abnormal expansion of GCN triplets within the PABPN1 gene. Previous descriptions ...
Transaminases increase: A manifestation of Duchenne's muscular dystrophy Aumento de transaminasas: Una manifestación de distrofia muscular de Duchenne
(2012)
Commonly used in clinical practice, glutamic oxalacetic (GOT) and glutamic piruvic (GPT) transaminases are produced in various body tissues, including striated muscle, so their blood elevation is not due exclusively to ...
Survival of patients with duchenne muscular dystrophy Sobrevida de pacientes con distrofia muscular de duchenne
(Sociedad Chilena de Pediatria, 2018)
© 2018, Sociedad Chilena de Pediatria. All rights reserved. Introduction: Duchenne muscular dystrophy (DMD) leads to a progressive deterioration of the muscle function and premature death. There are no longitudinal studies ...
Combined therapies for Duchenne muscular dystrophy to optimize treatment efficacy
(Frontiers Media, 2018-04)
Duchene Muscular Dystrophy (DMD) is the most frequent muscular dystrophy and one of the most severe due to the absence of the dystrophin protein. Typical pathological features include muscle weakness, muscle wasting, ...
Pain characterization in Duchenne muscular dystrophy
(Assoc Arquivos Neuro- Psiquiatria, 2016)
Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder, characterized by progressive muscle weakness. Historically, pain has not been considered to be a major symptom in DMD. Objective: To investigate the ...
Involvement of organic systems in golden retriever X-linked muscular dystrophy
(2011-07-01)
Duchenne muscular dystrophy is a lethal genetic disease characterized by progressive muscle degeneration that usually had been used the Golden Retriever as a model for studying the disease (GRMD - Golden Retriever Muscular ...