نتایج جستجو برای: melas syndrome

تعداد نتایج: 622265  

Journal: :Journal of fish biology 2010
M Nowak J Kosco W Popek P Epler

The North American catfish, the black bullhead Ameiurus melas, is recorded for the first time in Poland. The origin of these fish is not clear, but their presence may be associated with unregulated introductions by anglers.

Journal: :Academic Journal of Gastroenterology & Hepatology 2020

2016
Sara Seitun Laura Massobrio Anna Rubegni Claudia Nesti Margherita Castiglione Morelli Sara Boccalini Athena Galletto Pregliasco Irilda Budaj Luca Deferrari Gian Marco Rosa Fabrizio Montecucco Alberto Valbusa

A 49-year-old man presented with chest pain, dyspnea, and lactic acidosis. Left ventricular hypertrophy and myocardial fibrosis were detected. The sequencing of mitochondrial genome (mtDNA) revealed the presence of A to G mtDNA point mutation at position 3243 (m.3243A>G) in tRNALeu(UUR) gene. Diagnosis of cardiac involvement in a patient with Mitochondrial Encephalomyopathy, Lactic Acidosis, an...

Journal: :Biochemical Society symposium 1999
S M Rothman

Mitochondria possess their own DNA and transcription and translation machinery for the synthesis of 13 protein subunits for the oxidative phosphorylation system, two rRNAs and 22 tRNAs. In 1988 the first human neurodegenerative diseases associated with mutations in the mitochondrial genome were described. The most recent biochemical and genetic research suggests that mitochondrial disorders are...

2012
Juliana Gamba Luana T. Gamba Gabriela S. Rodrigues Beatriz H. Kiyomoto Carlos T. Moraes Celia H. Tengan

Nitric oxide (NO) is a free radical and a signaling molecule in several pathways, produced by nitric oxide synthase (NOS) from the conversion of L-arginine to citrulline. Supplementation of L-arginine has been used to treat MELAS (mitochondrial encephalopathy with lactic acidosis and stroke like syndrome), a mitochondrial disease caused by the m.3243A>G mutation. Low levels of serum arginine an...

Journal: :Archives of neurology 2005
Liana G Apostolova Matthew White Steven A Moore Patricia H Davis

BACKGROUND Myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome typically manifests in adults younger than 40 years with encephalopathy, stroke-like episodes, and lactic acidosis. Magnetic resonance imaging (MRI) abnormalities typically involve the cortical gray and the adjacent subcortical white matter. OBJECTIVE To describe a 58-year-old woman diagnosed with ...

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