Fatal Rhabdomyolysis in 2 Children with LPIN1 Mutations-Reference-Cited by-同舟云学术

Fatal Rhabdomyolysis in 2 Children with LPIN1 Mutations

Published:2012-06 Issue:6 Volume:160 Page:1052-1054
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Bergounioux Jean,Brassier Anais,Rambaud Caroline,Bustarret Olivier,Michot Caroline,Hubert Laurence,Arnoux Jean Baptiste,Laquerriere Annie,Bekri Soumeya,Galene-Gromez Sophie,Bonnet Damien,Hubert Philippe,de Lonlay Pascale

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference8 articles.

1. LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood;Michot;Hum Mutat,2010

2. Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood;Zeharia;Am J Hum Genet,2008

3. ABCs of clinical electrocardiography: conditions not primarily affecting the heart;Slovis;BMJ,2002

4. The Saccharomyces cerevisiae Lipin homolog is a Mg2+-dependent phosphatidate phosphatase enzyme;Han;J Biol Chem,2006

5. Cardiac lipin 1 expression is regulated by the peroxisome proliferator activated receptor γ coactivator 1α/estrogen related receptor axis;Mitra;J Mol Cell Cardiol,2011

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1. Cellular mechanisms of acute rhabdomyolysis in inherited metabolic diseases;Journal of Inherited Metabolic Disease;2024-08-12

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3. Hydroxychloroquine sulfate: A novel treatment for lipin-1 deficiency?;Biomedicine & Pharmacotherapy;2023-07

4. Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency;Molecular Genetics and Metabolism Reports;2023-06

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