Heart Disease in Mothers of Children with Duchenne Muscular Dystrophy
RMF Lisboa da Silva - Current Cardiology Reviews, 2024 - benthamdirect.com
Female carriers of Duchenne Muscular Dystrophy (DMD) carry a heterozygous pathogenic
variant in the dystrophin gene and can transmit pathogenic variants to their offspring. DMD is …
variant in the dystrophin gene and can transmit pathogenic variants to their offspring. DMD is …
Asymmetric Myocardial Involvement as an Early Indicator of Cardiac Dysfunction in Pediatric Dystrophinopathies: A Study on Cardiac Magnetic Resonance (CMR) …
R Esmel-Vilomara, L Riaza, L Costa-Comellas… - Pediatric …, 2024 - Springer
Dystrophinopathies, such as Duchenne and Becker muscular dystrophy, frequently lead to
cardiomyopathy, being its primary cause of mortality. Detecting cardiac dysfunction early is …
cardiomyopathy, being its primary cause of mortality. Detecting cardiac dysfunction early is …
Correction: Myocardial native T1 mapping and extracellular volume quantification in asymptomatic female carriers of Duchenne muscular dystrophy gene mutations.
L Masárová, R Panovský, M Pešl… - Orphanet Journal of …, 2023 - search.ebscohost.com
The mean global native T1 relaxation time was similar for DMD-FC and CG (1005.1±26.3 ms
vs. 1003.5±25 ms; p-value= 0.81)(Fig. 1), as well as the mean global ECV value …
vs. 1003.5±25 ms; p-value= 0.81)(Fig. 1), as well as the mean global ECV value …
Contrast-Enhanced Magnetic Resonance Imaging Based T1 Mapping and Extracellular Volume Fractions Are Associated with Peripheral Artery Disease
AI Fitian, MC Shieh, OA Gimnich, T Belousova… - Journal of …, 2024 - mdpi.com
Background: Extracellular volume fraction (ECV), measured with contrast-enhanced
magnetic resonance imaging (CE-MRI), has been utilized to study myocardial fibrosis, but its …
magnetic resonance imaging (CE-MRI), has been utilized to study myocardial fibrosis, but its …
Мышечная дистрофия, связанная с геном DMD, у женщин
ЕО Воронцова, ЕВ Зинина… - Нервно-мышечные …, 2024 - nmb.abvpress.ru
Аннотация Дистрофинопатии–спектр Х-сцепленных мышечных заболеваний,
связанных с патогенными/вероятно патогенными вариантами в гене дистрофина …
связанных с патогенными/вероятно патогенными вариантами в гене дистрофина …