Literature DB >> 24105666

Absence of G1528C mutation in long-chain 3-hydroxyacyl-CoA dehydrogenase in four Indian patients with pregnancy-related liver disease.

V Raghupathy1, Ashish Goel, Kavitha R Thangaraj, C E Eapen, K A Balasubramanian, Annie Regi, Ruby Jose, Santosh J Benjamin, Anup Ramachandran.   

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Year:  2014        PMID： 24105666     DOI： 10.1007/s12664-013-0408-0

Source DB:  PubMed          Journal:  Indian J Gastroenterol        ISSN： 0254-8860


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  10 in total

1.  How accurate are the Swansea criteria to diagnose acute fatty liver of pregnancy in predicting hepatic microvesicular steatosis?

Authors:  A Goel; B Ramakrishna; U Zachariah; J Ramachandran; C E Eapen; G Kurian; G Chandy
Journal:  Gut       Date:  2010-10-11       Impact factor: 23.059

2.  Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy.

Authors:  A M Innes; L E Seargeant; K Balachandra; C R Roe; R J Wanders; J P Ruiter; O Casiro; D A Grewar; C R Greenberg
Journal:  Pediatr Res       Date:  2000-01       Impact factor: 3.756

3.  Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene.

Authors:  L IJlst; J P Ruiter; J M Hoovers; M E Jakobs; R J Wanders
Journal:  J Clin Invest       Date:  1996-08-15       Impact factor: 14.808

4.  Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

Authors:  T Tyni; A Palotie; L Viinikka; L Valanne; M K Salo; U von Döbeln; S Jackson; R Wanders; N Venizelos; H Pihko
Journal:  J Pediatr       Date:  1997-01       Impact factor: 4.406

5.  Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

Authors:  W R Treem; M E Shoup; D E Hale; M J Bennett; P Rinaldo; D S Millington; C A Stanley; C A Riely; J S Hyams
Journal:  Am J Gastroenterol       Date:  1996-11       Impact factor: 10.864

6.  No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.

Authors:  Xiao-Fei Kong; Xin-Xin Zhang; Ying-Yan Yu; Qing Shi; Duan-Duan La; Chuan-De Zhu-Ge; Lin Deng; Qi-Ming Gong; Bai-Yong Shen; Cheng-Hong Peng; Hong-Wei Li
Journal:  J Gastroenterol Hepatol       Date:  2007-12       Impact factor: 4.029

7.  A prospective national study of acute fatty liver of pregnancy in the UK.

Authors:  M Knight; C Nelson-Piercy; J J Kurinczuk; P Spark; P Brocklehurst
Journal:  Gut       Date:  2008-03-10       Impact factor: 23.059

8.  Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein.

Authors:  L IJlst; R J Wanders; S Ushikubo; T Kamijo; T Hashimoto
Journal:  Biochim Biophys Acta       Date:  1994-12-08

Review 9.  Liver disease in pregnancy.

Authors:  J Eileen Hay
Journal:  Hepatology       Date:  2008-03       Impact factor: 17.425

10.  Evidence for fatty acid oxidation in human placenta, and the relationship of fatty acid oxidation enzyme activities with gestational age.

Authors:  D Rakheja; M J Bennett; B M Foster; R Domiati-Saad; B B Rogers
Journal:  Placenta       Date:  2002-05       Impact factor: 3.481
  10 in total

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