Literature DB >> 11593134

A rare cause of hepatomegaly: 3-hydroxy-3-methylglutaryl coenzyme-a lyase deficiency.

N Urgançi1, M Arapoğlu, M Evrüke, A Aydin.   

Abstract

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Year:  2001        PMID： 11593134     DOI： 10.1097/00005176-200109000-00022

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN： 0277-2116            Impact factor:   2.839


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  4 in total

1.  Induction of a Proinflammatory Response in Cortical Astrocytes by the Major Metabolites Accumulating in HMG-CoA Lyase Deficiency: the Role of ERK Signaling Pathway in Cytokine Release.

Authors:  Carolina Gonçalves Fernandes; Marília Danyelle Nunes Rodrigues; Bianca Seminotti; Ana Laura Colín-González; Abel Santamaria; André Quincozes-Santos; Moacir Wajner
Journal:  Mol Neurobiol       Date:  2015-06-23       Impact factor: 5.590

2.  Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria.

Authors:  Beatriz Puisac; María Arnedo; Cesar H Casale; María Pilar Ribate; Tomás Castiella; Feliciano J Ramos; Antonia Ribes; Celia Pérez-Cerdá; Nuria Casals; Fausto G Hegardt; Juan Pié
Journal:  J Inherit Metab Dis       Date:  2010-06-08       Impact factor: 4.982

3.  Hepatic Manifestations of 3-Hydroxy-3-Methylglutaryl-Coenzyme-A Lyase Deficiency in Saudi Patients: Experience of a Tertiary Care Center.

Authors:  Sinan Holdar; Zuhair Rahbeeni; Khushnooda Ramzan; Faiqa Imtiaz
Journal:  J Pediatr Genet       Date:  2020-07-29

4.  A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency.

Authors:  Francesca Santarelli; Michela Cassanello; Ausilia Enea; Francesca Poma; Valentina D'Onofrio; Giovanna Guala; Giangiacomo Garrone; Paola Puccinelli; Ubaldo Caruso; Francesco Porta; Marco Spada
Journal:  Ital J Pediatr       Date:  2013-05-24       Impact factor: 2.638
  4 in total

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