Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNAIle mutation-Reference-Cited by-同舟云学术

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Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNAIle mutation

Published:2011-04 Issue:1-2 Volume:303 Page:39-42
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Emmanuele Valentina,Sotiriou Evangelia,Shirazi Maryam,Tanji Kurenai,Haller Ronald G.,Heinicke Katja,Bosch Peter E.,Hirano Michio,DiMauro Salvatore

Funder

NIH

Marriott Mitochondrial Disorder Clinical Research Fund (MMDCRF)

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference39 articles.

1. Rhabdomyolysis and acute kidney injury;Bosch;New Engl J Med,2009

2. A diagnostic algorithm for metabolic myopathies;Berardo;Curr Neurol Neurosci Rep,2010

3. A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria;Andreu;Ann Neurol,1999

4. A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis;McFarland;Neuromuscul Disord,2004

5. Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mtDNA;Karadimas;Neurology,2000

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2. Clinicogenetical Variants of Progressive External Ophthalmoplegia - An Especial Review of Non-ophthalmic Manifestations;Neurology India;2020

3. Lethal neonatal mitochondrial phenotype caused by a novel polymerase subunit gamma mutation;Medicine;2018-10

4. Myopathology of Adult and Paediatric Mitochondrial Diseases;Journal of Clinical Medicine;2017-07-04

5. Perspectives on Exertional Rhabdomyolysis;Sports Medicine;2017-03

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