Articles with "patients dmd" as a keyword



The effects of glucocorticoids on cardiac function of patients with Duchenne muscular dystrophy: benefit or not?

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Published in 2025 at "European Journal of Pediatrics"

DOI: 10.1007/s00431-025-06141-5

Abstract: Duchenne muscular dystrophy (DMD) is a progressive, incurable X-linked neuromuscular disease caused by mutations in the dystrophin gene, resulting in functional dystrophin deficiency. Currently, cardiovascular complications are the leading cause of death in patients with… read more here.

Keywords: cardiac function; function patients; glucocorticoids cardiac; function ... See more keywords

One in five patients with Duchenne muscular dystrophy dies from other causes than cardiac or respiratory failure

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Published in 2021 at "European Journal of Epidemiology"

DOI: 10.1007/s10654-021-00819-4

Abstract: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder with increasing life expectancy from late teens to over 30 years of age. The aim of this nationwide study was to explore the prevalence, life expectancy… read more here.

Keywords: patients dmd; death; duchenne muscular; muscular dystrophy ... See more keywords

Histopathologic Changes of the Esophagus in Duchenne Muscular Dystrophy.

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Published in 2023 at "International journal of surgical pathology"

DOI: 10.1177/10668969231167532

Abstract: Duchenne muscular dystrophy (DMD) is characterized by progressive systemic muscle wasting, leading to respiratory paralysis and early death. This X-linked disease is caused by DMD mutations, encoding dystrophin.1 There is little information regarding gastrointestinal abnormalities… read more here.

Keywords: patients dmd; duchenne muscular; dystrophy; histopathologic changes ... See more keywords

Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy

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Published in 2022 at "PLOS ONE"

DOI: 10.1371/journal.pone.0276640

Abstract: Introductions Duchenne muscular dystrophy (DMD) is an X-linked recessive progressive muscular disease marked by developmental delays due to mutations in the DMD gene, which encodes dystrophin. Brain comorbidity adds to the burden of limited mobility… read more here.

Keywords: intellectual disability; patients dmd; duchenne muscular; disability ... See more keywords

The Association Between Physical Activity/Heart Rate Variability Data Obtained Using a Wearable Device and Timed Motor Functional Tests in Patients with Duchenne Muscular Dystrophy: A Pilot Study

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Published in 2024 at "Journal of Neuromuscular Diseases"

DOI: 10.3233/jnd-230142

Abstract: Background: Duchenne muscular dystrophy (DMD) is a devastating X-linked muscle disease. Clinical evaluation of DMD uses patient-intensive motor function tests, and the recent development of wearable devices allows the collection of a variety of biometric… read more here.

Keywords: physical activity; patients dmd; heart rate; activity ... See more keywords

Survival of patients with Duchenne muscular dystrophy.

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Published in 2018 at "Revista chilena de pediatria"

DOI: 10.4067/s0370-41062018005000704

Abstract: INTRODUCTION Duchenne muscular dystrophy (DMD) leads to a progressive deterioration of the mus cle function and premature death. There are no longitudinal studies on the course of this pathology in Chile. OBJECTIVE To determine survival… read more here.

Keywords: patients dmd; age; muscular dystrophy; survival ... See more keywords