نتایج جستجو برای: dreifuss

تعداد نتایج: 967  

Journal: :genetics in the 3rd millennium 0
غلامرضا زمانی gholamreza zamani child neurologist, children's medical center, tehran university of medical sciences (tums)

muscular dystrophies are inherited disorders that cause progressive muscle weakness (myopathy) and atrophy (loss of muscle mass) due to defects in one or more genes required for normal muscle function. some of the genes responsible for these conditions have been identified .there are a number of different types of muscular dystrophy. the primary symptom for most types is muscle weakness, althou...

2012
Vincenzo Russo Anna Rago Luisa Politano Andrea Antonio Papa Federica Di Meo Maria Giovanna Russo Paolo Golino Raffaele Calabrò Gerardo Nigro

BACKGROUND Sudden cardiac death (SCD) is common in patients with Emery-Dreifuss muscular dystrophy (EDMD) and is attributed to the development of life-threatening arrhythmias that occur in the presence of normal left ventricular systolic function. Heterogeneity of ventricular repolarization is considered to provide an electrophysiological substrate for malignant arrhythmias. QTc dispersion (QTc...

Journal: :Revista Portuguesa de Cardiologia (English Edition) 2012

Journal: :The Journal of clinical investigation 2007
Antoine Muchir Paul Pavlidis Valérie Decostre Alan J Herron Takuro Arimura Gisèle Bonne Howard J Worman

Mutations in LMNA, which encodes nuclear Lamins A and C cause diseases affecting various organs, including the heart. We have determined the effects of an Lmna H222P mutation on signaling pathways involved in the development of cardiomyopathy in a knockin mouse model of autosomal dominant Emery-Dreifuss muscular dystrophy. Analysis of genome-wide expression profiles in hearts using Affymetrix G...

Journal: :Journal of medical genetics 1986
N S Thomas H Williams L J Elsas L C Hopkins M Sarfarazi P S Harper

The linkage relationships of the gene for Emery-Dreifuss muscular dystrophy have been analysed in a large American kindred using DNA probes from different regions of the X chromosome. Close linkage was found with the locus for factor VIII, with no recombinants in 12 opportunities (maximum lod score 4.3), and with locus DXS15 (two recombinants in 17 opportunities, maximum lod score 2.9 at 0 = 10...

Journal: :Annals of nuclear medicine 2005
Takashi Fujiita Masami Shimizu Bunji Kaku Hounin Kanaya Yuki Horita Yoshihide Uno Tsukasa Yamazaki Takio Ohka Kenji Sakata Hiroshi Mabuchi

A 33-year-old man was admitted for general malaise and vomiting. An electrocardiogram showed a complete atrioventricular block and an echocardiogram showed right atrial dilatation and normal wall motion of left ventricle (LV). Gene analysis showed nonsense mutation in the STA gene, which codes for emerin, and Emery-Dreifuss muscular dystrophy was diagnosed. An endomyocardial biopsy of right ven...

Journal: :international journal of molecular and cellular medicine 0
azadeh ahmadifard department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) javad jamshidi noncommunicable diseases research center, fasa university of medical sciences, fasa, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی فسا (fasa university of medical sciences) abbas tafakhori department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) zeinab falsafi department of neurology, school of medicine, imam khomeini hospital and iranian center of neurological research, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) hossein darvish department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

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Journal: :Canadian Medical Association Journal 2018

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