Literature DB >> 4446691

Hyperammonemia through deficiency of ornithine carbamyl transferase.

J P Farriaux, J L Dhondt, L Cathelineau, J Ratel, G Fontaine.   

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Year:  1974        PMID: 4446691     DOI: 10.1007/BF00464614

Source DB:  PubMed          Journal:  Z Kinderheilkd        ISSN: 0044-2917


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  26 in total

1.  [Chromosome X transmission of the ornithine-carbamyl-transferase structural gene. A study of 3 families].

Authors:  L Cathelineau; J M Saudubray; J Navarro; C Polonovski
Journal:  Ann Genet       Date:  1973-09

2.  Biochemical investigations of hyperammonaemia.

Authors:  B Levin; V G Oberholzer; L Sinclair
Journal:  Lancet       Date:  1969-07-26       Impact factor: 79.321

3.  [Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy].

Authors:  J M Saudubray; L Cathelineau; C Charpentier; J Boisse; C Allaneau; H Le Bont; B Lesage
Journal:  Arch Fr Pediatr       Date:  1973-01

4.  Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.

Authors:  E M Short; H O Conn; P J Snodgrass; A G Campbell; L E Rosenberg
Journal:  N Engl J Med       Date:  1973-01-04       Impact factor: 91.245

5.  Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males.

Authors:  A G Campbell; L E Rosenberg; P J Snodgrass; C T Nuzum
Journal:  N Engl J Med       Date:  1973-01-04       Impact factor: 91.245

6.  Ornithine carbamyl transferase: the effects of pH on the kinetics of a mutant human enzyme.

Authors:  L Cathelineau; J M Saudubray; C Polonovski
Journal:  Clin Chim Acta       Date:  1972-10       Impact factor: 3.786

7.  [Congenital hyperammoniemia caused by ornithine carbamoyl-transferase and carbamyl phosphate synthetase deficiency].

Authors:  B Salle; B Levin; B Longin; P Richard; M Andre; J Gauthier
Journal:  Arch Fr Pediatr       Date:  1972-05

8.  Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.

Authors:  L M Corbeel; J P Colombo; M Van Sande; A Weber
Journal:  Arch Dis Child       Date:  1969-12       Impact factor: 3.791

Review 9.  Hereditary metabolic disorders of the urea cycle.

Authors:  B Levin
Journal:  Adv Clin Chem       Date:  1971       Impact factor: 5.394

10.  Arginosuccine aciduria.

Authors:  B Levin
Journal:  Am J Dis Child       Date:  1967-01
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  3 in total

1.  Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency.

Authors:  C van der Heiden; H D Bakker; J Desplanque; M Brink; P K de Bree; S K Wadman
Journal:  Eur J Pediatr       Date:  1978-07-19       Impact factor: 3.183

2.  Liver pathology in a new congenital disorder of urea synthesis: N-acetylglutamate synthetase deficiency.

Authors:  A Zimmermann; C Bachmann; G Schubiger
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

3.  Profiling and Identification of Novel Immunogenic Proteins of Staphylococcus hyicus ZC-4 by Immunoproteomic Assay.

Authors:  Lei Wang; Zhi-Wei Wu; Yan Li; Jian-Guo Dong; Le-Yi Zhang; Peng-Shuai Liang; Yan-Ling Liu; Ya-Hua Zhao; Chang-Xu Song
Journal:  PLoS One       Date:  2016-12-08       Impact factor: 3.240

  3 in total

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