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About 310 results

ALLMedicine™ Dystrophinopathies Center

Research & Reviews  155 results

A deep learning model for diagnosing dystrophinopathies on thigh muscle MRI images.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798322
BMC Neurology; Yang M, Zheng Y et. al.

Jan 12th, 2021 - Dystrophinopathies are the most common type of inherited muscular diseases. Muscle biopsy and genetic tests are effective to diagnose the disease but cost much more than primary hospitals can reach. The more available muscle MRI is promising but i...

Validation of the EULAR/ACR 2017 idiopathic inflammatory myopathy classification criter...
https://www.ncbi.nlm.nih.gov/pubmed/33337999
Clinical and Experimental Rheumatology; Sag E, Demir S et. al.

Dec 18th, 2020 - In 2017, a new set of criteria was proposed by EULAR/ACR to classify idiopathic inflammatory myopathies. Our aim was to validate the EULAR/ACR 2017 classification criteria in juvenile dermatomyositis (JDM) patients. This study was carried out at H...

Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise ...
https://doi.org/10.1136/jmedgenet-2020-107113
Journal of Medical Genetics; Xie Z, Sun C et. al.

Sep 26th, 2020 - To investigate the diagnostic value of implementing a stepwise genetic testing strategy (SGTS) in genetically unsolved cases with dystrophinopathies. After routine genetic testing in 872 male patients with highly suspected dystrophinopathies, we i...

12-Month changes of muscle strength, body composition and physical activity in adults w...
https://doi.org/10.1080/09638288.2020.1808087
Disability and Rehabilitation; Jacques MF, Onambele-Pearson GL et. al.

Aug 27th, 2020 - Muscular dystrophy (MD) is an umbrella term for muscle wasting conditions, for which longitudinal changes in function and body composition are well established in children with Duchenne (DMD), however, changes in adults with DMD and Beckers (BMD),...

X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular ch...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412789
Skeletal Muscle; Barthélémy I, Calmels N et. al.

Aug 9th, 2020 - Canine models of Duchenne muscular dystrophy (DMD) are a valuable tool to evaluate potential therapies because they faithfully reproduce the human disease. Several cases of dystrophinopathies have been described in canines, but the Golden Retrieve...

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Clinicaltrials.gov  155 results

A deep learning model for diagnosing dystrophinopathies on thigh muscle MRI images.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798322
BMC Neurology; Yang M, Zheng Y et. al.

Jan 12th, 2021 - Dystrophinopathies are the most common type of inherited muscular diseases. Muscle biopsy and genetic tests are effective to diagnose the disease but cost much more than primary hospitals can reach. The more available muscle MRI is promising but i...

Validation of the EULAR/ACR 2017 idiopathic inflammatory myopathy classification criter...
https://www.ncbi.nlm.nih.gov/pubmed/33337999
Clinical and Experimental Rheumatology; Sag E, Demir S et. al.

Dec 18th, 2020 - In 2017, a new set of criteria was proposed by EULAR/ACR to classify idiopathic inflammatory myopathies. Our aim was to validate the EULAR/ACR 2017 classification criteria in juvenile dermatomyositis (JDM) patients. This study was carried out at H...

Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise ...
https://doi.org/10.1136/jmedgenet-2020-107113
Journal of Medical Genetics; Xie Z, Sun C et. al.

Sep 26th, 2020 - To investigate the diagnostic value of implementing a stepwise genetic testing strategy (SGTS) in genetically unsolved cases with dystrophinopathies. After routine genetic testing in 872 male patients with highly suspected dystrophinopathies, we i...

12-Month changes of muscle strength, body composition and physical activity in adults w...
https://doi.org/10.1080/09638288.2020.1808087
Disability and Rehabilitation; Jacques MF, Onambele-Pearson GL et. al.

Aug 27th, 2020 - Muscular dystrophy (MD) is an umbrella term for muscle wasting conditions, for which longitudinal changes in function and body composition are well established in children with Duchenne (DMD), however, changes in adults with DMD and Beckers (BMD),...

X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular ch...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412789
Skeletal Muscle; Barthélémy I, Calmels N et. al.

Aug 9th, 2020 - Canine models of Duchenne muscular dystrophy (DMD) are a valuable tool to evaluate potential therapies because they faithfully reproduce the human disease. Several cases of dystrophinopathies have been described in canines, but the Golden Retrieve...

see more →