نتایج جستجو برای: dmd 6636 percent

تعداد نتایج: 101855  

2017
Hao Yu Yu-Chao Chen Gong-Lu Liu Zhi-Ying Wu

BACKGROUND Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive neuromuscular diseases resulting from dystrophin (DMD) gene mutations. It has been known that the carrier of DMD mutations may also have symptoms of the disease. While de novo mutation is quite common in BMD/DMD patients, it is rarely reported in the female carriers. METHODS Two sporadic Ch...

Journal: :Journal of neuropathology and experimental neurology 2010
Lan Zhou Haiyan Lu

Duchenne muscular dystrophy (DMD) is the most common genetic muscle disease affecting 1 in 3,500 live male births. It is an X-linked recessive disease caused by a defective dystrophin gene. The disease is characterized by progressive limb weakness, respiratory and cardiac failure, and premature death. Fibrosis is a prominent pathological feature of muscle biopsies from patients with DMD. It dir...

2011
Tae-Jin Song Kyung-A Lee Seong-Woong Kang Hanna Cho Young-Chul Choi

Duchenne muscular dystrophy usually affects males. However, females are also affected in rare instances. Approximately 8% of female Duchenne muscular dystrophy (DMD) carriers are manifesting carriers and have muscle weakness to some extent. We investigated the clinical features of 3 female patients with dystrophinopathy diagnosed by clinical, pathological, and genetic studies at our neuromuscul...

2017
Mayra Priscila Boscolo Alvarez Talita Dias da Silva Francis Meire Favero Vitor Engrácia Valenti Rodrigo Daminello Raimundo Luiz Carlos Marques Vanderlei David M Garner Carlos Bandeira de Mello Monteiro

INTRODUCTION Duchenne Muscular Dystrophy (DMD) is characterized by progressive muscle weakness that can lead to disability. Owing to functional difficulties faced by individuals with DMD, the use of assistive technology is essential to provide or facilitate functional abilities. In DMD, cardiac autonomic dysfunction has been reported in addition to musculoskeletal impairment. Consequently, the ...

Journal: :RNA 2007
Annemieke Aartsma-Rus Gert-Jan B van Ommen

Antisense-mediated modulation of splicing is one of the few fields where antisense oligonucleotides (AONs) have been able to live up to their expectations. In this approach, AONs are implemented to restore cryptic splicing, to change levels of alternatively spliced genes, or, in case of Duchenne muscular dystrophy (DMD), to skip an exon in order to restore a disrupted reading frame. The latter ...

Journal: :Journal of neuromuscular diseases 2015
Erik Landfeldt Peter Lindgren Michela Guglieri Hanns Lochmüller Katharine Bushby

BACKGROUND International care guidelines for Duchenne muscular dystrophy (DMD) were published in 2010, but compliance in clinical practice is unknown. OBJECTIVE The objective of our study was to compare real-world DMD care in Germany, Italy, the UK, and the US with the clinical recommendations. METHODS DMD patients from Germany, Italy, the UK, and the US were identified through Translationa...

Journal: :Annals of neurology 2012
Jerry R Mendell Chris Shilling Nancy D Leslie Kevin M Flanigan Roula al-Dahhak Julie Gastier-Foster Kelley Kneile Diane M Dunn Brett Duval Alexander Aoyagi Cindy Hamil Maha Mahmoud Kandice Roush Lauren Bird Chelsea Rankin Heather Lilly Natalie Street Ram Chandrasekar Robert B Weiss

OBJECTIVE Creatine kinase (CK) levels are increased on dried blood spots in newborns related to the birthing process. As a marker for newborn screening, CK in Duchenne muscular dystrophy (DMD) results in false-positive testing. In this report, we introduce a 2-tier system using the dried blood spot to first assess CK with follow-up DMD gene testing. METHODS A fluorometric assay based upon the...

Journal: :CoRR 2016
Seth D. Pendergrass J. Nathan Kutz Steven L. Brunton

This work develops a parallelized algorithm to compute the dynamic mode decomposition (DMD) on a graphics processing unit using the streaming method of snapshots singular value decomposition. This allows the algorithm to operate efficiently on streaming data by avoiding redundant inner-products as new data becomes available. In addition, it is possible to leverage the native compressed format o...

2013
Ryan D. Wuebbles Apurva Sarathy Joe N. Kornegay Dean J. Burkin

Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease for which there is no cure and limited treatment options. Prednisone is currently the first line treatment option for DMD and studies have demonstrated that it improves muscle strength. Although prednisone has been used for the treatment of DMD for decades, the mechanism of action of this drug remains unclear. Recent studies hav...

2014
Chiara Pecori Marta Giannini Emilio Portaccio Angelo Ghezzi Bahia Hakiki Luisa Pastò Lorenzo Razzolini Andrea Sturchio Laura De Giglio Carlo Pozzilli Damiano Paolicelli Maria Trojano Maria Giovanna Marrosu Francesco Patti Gian Luigi Mancardi Claudio Solaro Rocco Totaro Maria Rosaria Tola Giovanna De Luca Alessandra Lugaresi Lucia Moiola Vittorio Martinelli Giancarlo Comi Maria Pia Amato

BACKGROUND Most of Multiple Sclerosis (MS) patients undergo disease modifying drug (DMD) therapy at childbearing age. The objective of this prospective, collaborative study, was to assess outcomes of pregnancies fathered by MS patients undergoing DMD. METHODS Structured interviews on pregnancies fathered by MS patients gathered in the Italian Pregnancy Dataset were collected; pregnancies were...

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