Literature DB >> 8295421

Sudden onset of ornithine carbamoyltransferase deficiency after aspirin ingestion.

I Yoshida1, M Yoshino, J Watanabe, F Yamashita.   

Abstract

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Year:  1993        PMID： 8295421     DOI： 10.1007/BF00714301

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  A case of ornithine transcarbamylase deficiency with acute and late onset simulating Reye's syndrome in an adult male.

Authors:  K Mizoguchi; K Sukehiro; M Ogata; S Onizuka; J Watanabe; I Yoshida; M Yoshino
Journal:  Kurume Med J       Date:  1990

2.  Public Health Service study of Reye's syndrome and medications. Report of the main study.

Authors:  E S Hurwitz; M J Barrett; D Bregman; W J Gunn; P Pinsky; L B Schonberger; J S Drage; R A Kaslow; D B Burlington; G V Quinnan
Journal:  JAMA       Date:  1987-04-10       Impact factor: 56.272
  2 in total
  3 in total

Review 1.  Non-traumatic coma in children.

Authors:  F J Kirkham
Journal:  Arch Dis Child       Date:  2001-10       Impact factor: 3.791

Review 2.  Inborn errors of metabolism in the differential diagnosis of fatty liver disease.

Authors:  Yılmaz Yıldız; Hatice Serap Sivri
Journal:  Turk J Gastroenterol       Date:  2020-01       Impact factor: 1.852

3.  Paternal transmission and slow elimination of mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients.

Authors:  Sanae Numata; Eimei Harada; Yasuki Maeno; Isao Ueki; Yoriko Watanabe; Chieko Fujii; Takashi Yanagawa; Satoshi Takenaka; Toshiro Inoue; Shinkai Inoue; Terufumi Goushi; Tsutomu Yasutake; Toshihiko Mizuta; Makoto Yoshino
Journal:  J Hum Genet       Date:  2007-11-20       Impact factor: 3.172
  3 in total

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