نتایج جستجو برای: dmd 6636 percent

تعداد نتایج: 101855  

2003
Dana Dudley Walter Duncan John Slaughter

For the past six years, Digital Light Processing technology from Texas Instruments has made significant inroads in the projection display market. With products enabling the world’s smallest data and video projectors, HDTVs, and digital cinema, DLP technology is extremely powerful and flexible. At the heart of these display solutions is Texas Instruments Digital Micromirror Device (DMD), a semic...

Journal: :Journal of Biomedicine and Biotechnology 2002
Aziza Sbiti Fatiha El Kerch Abdelaziz Sefiani

Duchenne and Becker muscular dystrophy (DMD and BMD) are X-linked diseases resulting from a defect in the dystrophin gene located on Xp21. DMD is the most frequent neuromuscular disease in humans (1/3500 male newborn). Deletions in the dystrophin gene represent 65% of mutations in DMD/BMD patients. We have analyzed DNA from 72 Moroccan patients with DMD/BMD using the multiplex polymerase chain ...

Journal: :Human molecular genetics 2001
J C van Deutekom M Bremmer-Bout A A Janson I B Ginjaar F Baas J T den Dunnen G J van Ommen

Due to frame-shifting mutations in the DMD gene that cause dystrophin deficiency, Duchenne muscular dystrophy (DMD) patients suffer from lethal muscle degeneration. In contrast, mutations in the allelic Becker muscular dystrophy (BMD) do not disrupt the translational reading frame, resulting in a less severe phenotype. In this study, we explored a genetic therapy aimed at restoring the reading ...

Journal: :The Journal of molecular diagnostics : JMD 2011
Lisa Kalman Jay Leonard Norman Gerry Jack Tarleton Christina Bridges Julie M Gastier-Foster Robert E Pyatt Eileen Stonerock Monique A Johnson C Sue Richards Iris Schrijver Tianhui Ma Vanessa Rangel Miller Yetsa Adadevoh Pat Furlong Christine Beiswanger Lorraine Toji

Duchenne and Becker muscular dystrophies (DMD/BMD) are allelic X-linked recessive disorders that affect approximately 1 in 3500 and 1 in 20,000 male individuals, respectively. Approximately 65% of patients with DMD have deletions, 7% to 10% have duplications, and 25% to 30% have point mutations in one or more of the 79 exons of the dystrophin gene. Most clinical genetics laboratories test for d...

2017
Yan Weng Yu-ping Ren Li Zhang Xiao-dan Huang Xing-chao Shen-tu

BACKGROUND Descemet's membrane detachment (DMD) is one of the most serious complications of modern cataract surgery. We present an alternative technique for management of DMD with a review of the literature on current strategies for the treatment of DMD. CASE PRESENTATION A 74-year-old woman developed DMD after phacoemulsification and failed the first descemetopexy with air tamponade. An alte...

2015
Shih-Wen Wang Sung-Huei Tseng

We herein report two cases of occult Descemet's membrane detachment (DMD) after phacoemulsification surgery, which initially presented as persistent corneal edema and had been considered as pseudophakic bullous keratopathy. The patients were thus scheduled to receive corneal transplantation. For Case 1, DMD was incidentally detected by slit-lamp examination 2 months postoperatively, only when p...

Journal: :Neuroscience letters 2006
Marianne Jover Christina Schmitz Emmanuelle Bosdure Brigitte Chabrol Christine Assaiante

We investigated the consequences of a progressive damage to the muscular system on the organization of anticipatory postural adjustments (APA) in children with Duchenne muscular dystrophy (DMD). We used a bimanual load-lifting task requiring the stabilization of the forearm position despite its voluntary or imposed unloading. Eight children with DMD from 4 to 11 years of age were compared to ei...

Journal: :Archives of ophthalmology 2008
Bryan J Winn Shan C Lin Michael R Hee Cynthia S Chiu

Extensive Descemet membrane detachment (DMD) is a rare complication of intraocular surgery that can lead to corneal decompensation. Although DMD may resolve spontaneously, surgical repair frequently is required. The diagnosis may be difficult because corneal edema can obscure visualization of the Descemet membrane (DM). Ultrasonographic biomicroscopy (UBM) has been the standard for imaging DMD ...

Journal: :Human molecular genetics 2010
Maria Grazia Di Certo Nicoletta Corbi Georgios Strimpakos Annalisa Onori Siro Luvisetto Cinzia Severini Angelo Guglielmotti Enrico Maria Batassa Cinzia Pisani Aristide Floridi Barbara Benassi Maurizio Fanciulli Armando Magrelli Elisabetta Mattei Claudio Passananti

The absence of the cytoskeletal protein dystrophin results in Duchenne muscular dystrophy (DMD). The utrophin protein is the best candidate for dystrophin replacement in DMD patients. To obtain therapeutic levels of utrophin expression in dystrophic muscle, we developed an alternative strategy based on the use of artificial zinc finger transcription factors (ZF ATFs). The ZF ATF 'Jazz' was rece...

Journal: :Growth regulation 1991
D Rapaport G M Colletto M Vainzof M C Duaik M Zatz

Growth rate was assessed in 187 boys affected with Duchenne muscular dystrophy (DMD) and bone age in 127 among them. Patients' heights were compared with their normal sibs, with expected stature according to midparents' stature and with normal Brazilian children of comparable age. The results showed that DMD boys have a normal length and weight at birth, but a delayed growth starting during the...

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