نتایج جستجو برای: dmd 6636 percent

تعداد نتایج: 101855  

2013
Harumasa Nakamura En Kimura Madoka Mori-Yoshimura Hirofumi Komaki Yu Matsuda Kanako Goto Yukiko K Hayashi Ichizo Nishino Shin‘ichi Takeda Mitsuru Kawai

BACKGROUND Currently, clinical trials for new therapeutic strategies are being planned for Duchenne and Becker muscular dystrophies (DMD/BMD). However, it is difficult to obtain adequate numbers of patients in clinical trials. As solutions to these problems, patient registries are an important resource worldwide, especially in rare diseases such as DMD/BMD. METHODS We developed a national reg...

Journal: :Research in Applied Economics 2014

2011
Akinori Nakamura Shin'ichi Takeda

Duchenne muscular dystrophy (DMD) is a devastating X-linked muscle disorder characterized by muscle wasting which is caused by mutations in the DMD gene. The DMD gene encodes the sarcolemmal protein dystrophin, and loss of dystrophin causes muscle degeneration and necrosis. Thus far, therapies for this disorder are unavailable. However, various therapeutic trials based on gene therapy, exon ski...

Journal: :Journal of pediatric psychology 2003
Nancy E Nereo Robert J Fee Veronica J Hinton

OBJECTIVE To examine parental stress in mothers of boys with Duchenne muscular dystrophy (DMD). METHOD Stress and its predictors were examined in mothers of boys with DMD (n = 112). Comparisons were made with mothers of healthy children (n = 800), children with cerebral palsy (CP; n = 28), siblings of boys with DMD (n = 46), and longitudinally (n = 16). RESULTS The presence of problem child...

2014
Henriette J A van Ruiten Volker Straub Kate Bushby Michela Guglieri

BACKGROUND Over the last 30 years, there has been little improvement in the age of diagnosis of Duchenne muscular dystrophy (DMD) (mean age of 4.5-4.11 years). AIM To review the diagnostic process for DMD in boys without a family history in order to identify where delays occur and suggest areas for improvement. DESIGN A retrospective case note review. SETTING A tertiary centre for neuromu...

2013
Hyeyoung Lee Dong Wook Jekarl Joonhong Park Hyojin Chae Myungshin Kim Yonggoo Kim Jong in Lee

Duchenne Muscular dystrophy (DMD) is an X-linked recessive disorder caused by mutations in the dystrophin gene, which is located in Xp21. The majority of the identified mutations are large deletions and duplications, and gene dosage assays were developed for quantitative genomic screening of copy number variations. However, remaining 25% of the DMD are due to point mutations and require direct ...

Journal: :Optical Engineering 2022

Aero-optical beam control relies on the development of low-latency forecasting techniques to quickly predict wavefronts aberrated by turbulent boundary layer around an airborne optical system, and its study applies a multidomain need from astronomy microscopy for high-fidelity laser propagation. We leverage capabilities dynamic mode decomposition (DMD) — equation-free, data-driven method identi...

Journal: :Veterinary ophthalmology 2015
Màrian Matas Riera David Donaldson Simon Lawrence Priestnall

The aim of this article was to describe Descemet's membrane detachment (DMD) following phacoemulsification in five equine eyes and to review the human literature on this topic. In the last decade, there has been increased reporting of DMD in the human literature, in particular following cataract surgery. The natural history of DMD remains unknown and although various medical and surgical treatm...

2016
Hong-Hao Yu Heng Zhao Yu-Bo Qing Wei-Rong Pan Bao-Yu Jia Hong-Ye Zhao Xing-Xu Huang Hong-Jiang Wei

Dystrophinopathy, including Duchenne muscle dystrophy (DMD) and Becker muscle dystrophy (BMD) is an incurable X-linked hereditary muscle dystrophy caused by a mutation in the DMD gene in coding dystrophin. Advances in further understanding DMD/BMD for therapy are expected. Studies on mdx mice and dogs with muscle dystrophy provide limited insight into DMD disease mechanisms and therapeutic test...

2014
LORENZA MAGLIANO MARIA GRAZIA D'ANGELO GIUSEPPE VITA MARIKA PANE ADELE D'AMICO UMBERTO BALOTTIN CORRADO ANGELINI ROBERTA BATTINI LUISA POLITANO MELANIA PATALANO ALESSANDRA SAGLIOCCHI FEDERICA CIVATI ERIKA BRIGHINA GIAN LUCA VITA SONIA MESSINA MARIA SFRAMELI MARIA ELENA LOMBARDO ROBERTA SCALISE GIULIA COLIA MARIA CATTERUCCIA ANGELA BERARDINELLI MARIA CHIARA MOTTA ALESSANDRA GAIANI CLAUDIO SEMPLICINI LUCA BELLO GUJA ASTREA ANTONELLA ZACCARO MARIANNA SCUTIFERO

This study explored the burden in parents and healthy siblings of 4-17 year-old patients with Duchenne (DMD) and Becker (BMD) muscular dystrophies, and whether the burden varied according to clinical aspects and social resources. Data on socio-demographic characteristics, patient's clinical history, parent and healthy children burden, and on parent's social resources were collected using self-r...

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