نتایج جستجو برای: myopathies

تعداد نتایج: 2714  

Journal: :Ceskoslovenska patologie 2011
J Zámecník R Vytásek J Vencovský V Vilím

3-nitrotyrosine (3NT) is regarded as a "footprint" of nitric oxide generation. The study aimed at documenting the presence and distribution of 3-nitrotyrosine (3NT) in muscle tissue samples from patients with idiopathic inflammatory myopathies (IIM) as well as from those with non-inflammatory myopathies to consider whether polymyositis (PM) and dermatomyositis (DM) could be distinguished based ...

Journal: :Journal of cell science 2016
Chiara Scotton Matteo Bovolenta Elena Schwartz Maria Sofia Falzarano Elena Martoni Chiara Passarelli Annarita Armaroli Hana Osman Carmelo Rodolico Sonia Messina Elena Pegoraro Adele D'Amico Enrico Bertini Francesca Gualandi Marcella Neri Rita Selvatici Patrizia Boffi Maria Antonietta Maioli Hanns Lochmüller Volker Straub Katherine Bushby Tiziana Castrignanò Graziano Pesole Patrizia Sabatelli Luciano Merlini Paola Braghetta Paolo Bonaldo Paolo Bernardi Reghan Foley Sebahattin Cirak Irina Zaharieva Francesco Muntoni Daniele Capitanio Cecilia Gelfi Ekaterina Kotelnikova Anton Yuryev Michael Lebowitz Xiping Zhang Brian A Hodge Karyn A Esser Alessandra Ferlini

Collagen VI myopathies are genetic disorders caused by mutations in collagen 6 A1, A2 and A3 genes, ranging from the severe Ullrich congenital muscular dystrophy to the milder Bethlem myopathy, which is recapitulated by collagen-VI-null (Col6a1(-/-)) mice. Abnormalities in mitochondria and autophagic pathway have been proposed as pathogenic causes of collagen VI myopathies, but the link between...

Journal: :Neurology India 2005

Journal: :Nihon Naika Gakkai Zasshi 2008

Journal: :Journal of the Neurological Sciences 2019

Journal: :The Journal of nutrition 2005
Ellen L Burnham Marc Moss Thomas R Ziegler

Myopathies related to critical illness have received increasing recognition over the past decade and are common in patients even after a brief period in the intensive care unit. Recent studies have revealed that myopathies in the critically ill may in fact be more prevalent than neuropathies and that morbidity and mortality may be greater. Protein catabolism, an increase in urinary nitrogen los...

Journal: :Paediatric anaesthesia 2013
Robert P Brislin Mary C Theroux

The core myopathies are a subset of myopathies that present in infancy with hypotonia and muscle weakness. They were formerly considered a rare type of congenital myopathy but are now recognized as being more prevalent. Due to their genetic linkage to mutations in the ryanodine receptor gene (RYR1), core myopathies (in particular, central core disease) carry a high risk of malignant hyperthermi...

2013
Kimberly Amburgey Angela Bailey Jean H Hwang Mark A Tarnopolsky Carsten G Bonnemann Livija Medne Katherine D Mathews James Collins Jasper R Daube Gregory P Wellman Brian Callaghan Nigel F Clarke James J Dowling

BACKGROUND RYR1 mutations are typically associated with core myopathies and are the most common overall cause of congenital myopathy. Dominant mutations are most often associated with central core disease and malignant hyperthermia, and genotype-phenotype patterns have emerged from the study of these mutations that have contributed to the understanding of disease pathogenesis. The recent availa...

Journal: :genetics in the 3rd millennium 0
مرال توپوکو meral topcu prof of pediatrics, hacettepe university children’s hospital, department of pediatric neurology

metabolic myopathies are genetically inherited disorders of muscle energy production that result in skeletal muscle dysfunction. they are a large group of diseases with diverse inborn errors of metabolism, in particular muscle energy production, and including disorders of glycogen (lysosomal and non-lysosomal glycogenoses), lipid (disorders of fatty acid b-oxidation, primary carnitine deficienc...

Journal: :Current neurology and neuroscience reports 2008
Adele D'Amico Enrico Bertini

This review focuses on congenital myopathies, a distinct but markedly heterogeneous group of muscle disorders that present with muscle weakness and typically appear at birth or in infancy. These myopathies have characteristic histopathologic abnormalities on muscle biopsy, allowing a preliminary morphologic classification. Advances in molecular genetics have allowed a more rational classificati...

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