نتایج جستجو برای: myofibrillar myopathy

تعداد نتایج: 14255  

Journal: :Saudi medical journal 2004
Ayman A El-Menyar Jassim Al-Suwaidi Abdurrazak A Gehani Abdulbari Bener

The current study reports the first family with confirmed myofibrillar myopathy MFM in the Middle East and the third family worldwide. This study highlights the importance of considering MFM in young patients presenting with idiopathic cardiomyopathy, arrhythmia or atrioventricular block in the Gulf states. This is the first report that presented 2 different types of cardiomyopathy and 2 differ...

Journal: :Romanian journal of internal medicine = Revue roumaine de medecine interne 2010
Alexandra Bastian H H Goebel

UNLABELLED Protein aggregation has been identified in muscle fibres and, thus, in certain neuromuscular disorders. There are certain similarities between IBM and DRM: midlife or late-onset clinical symptoms, apparently of both sporadic and genetic background, morphologically autophagocytosis by vacuole formation, which is frequent in IBM though rare in DRM, and presence of tubulofilamentous agg...

Journal: :JAMA neurology 2015
Roula Ghaoui Sandra T Cooper Monkol Lek Kristi Jones Alastair Corbett Stephen W Reddel Merrilee Needham Christina Liang Leigh B Waddell Garth Nicholson Gina O'Grady Simranpreet Kaur Royston Ong Mark Davis Carolyn M Sue Nigel G Laing Kathryn N North Daniel G MacArthur Nigel F Clarke

IMPORTANCE To our knowledge, the efficacy of transferring next-generation sequencing from a research setting to neuromuscular clinics has never been evaluated. OBJECTIVE To translate whole-exome sequencing (WES) to clinical practice for the genetic diagnosis of a large cohort of patients with limb-girdle muscular dystrophy (LGMD) for whom protein-based analyses and targeted Sanger sequencing ...

Journal: :Brain : a journal of neurology 2005
Montse Olivé Lev G Goldfarb Alexey Shatunov Dirk Fischer Isidro Ferrer

Mutations in myotilin gene (MYOT) have been associated with variable syndromes including limb girdle muscular dystrophy type 1A (LGMD1A) and a subgroup of myofibrillar myopathy (MFM/MYOT). We studied six Spanish patients from three unrelated kindreds and seven patients without family history. Three previously reported and two novel disease-associated MYOT mutations were identified in this group...

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