Literature DB >> 4852321

Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families.

T Palmer, V G Oberholzer, E A Burgess, L J Butler, B Levin.   

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Year:  1974        PMID: 4852321      PMCID: PMC1648820          DOI: 10.1136/adc.49.6.443

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


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  18 in total

1.  Lethal neonatal hyperammonaemia due to complete ornithine-transcarbamylase deficiency.

Authors:  A G Campbell; L E Rosenberg; P J Snodgrass; C T Nuzum
Journal:  Lancet       Date:  1971-07-24       Impact factor: 79.321

2.  Biochemical investigations of hyperammonaemia.

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

3.  Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.

Authors:  P Sunshine; J E Lindenbaum; H L Levy; J M Freeman
Journal:  Pediatrics       Date:  1972-07       Impact factor: 7.124

4.  Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.

Authors:  I Matsuda; S Arashima; H Nambu; Y Takekoshi; M Anakura
Journal:  Pediatrics       Date:  1971-10       Impact factor: 7.124

5.  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

6.  Congenital hyperammonemia. Association with hyperglycinemia and decreased levels of carbamyl phosphate synthetase.

Authors:  J M Freeman; J F Nicholson; R T Schimke; L P Rowland; S Carter
Journal:  Arch Neurol       Date:  1970-11

7.  Hyperammonemia: a deficiency of liver ornithine transcarbamylase.

Authors:  E Nagayama; T Kitayama; H Oguchi; K Ogata; E Tamura
Journal:  Paediatr Univ Tokyo       Date:  1970-12

8.  Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.

Authors:  B Levin; J M Abraham; V G Oberholzer; E A Burgess
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

9.  Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.

Authors:  B Levin; R H Dobbs; E A Burgess; T Palmer
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

Review 10.  Hereditary metabolic disorders of the urea cycle.

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

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  2 in total

1.  Glutamine-valine index - An aid in the detection of urea-cycle disorders.

Authors:  A Briddon; V G Oberholzer
Journal:  Amino Acids       Date:  1991-06       Impact factor: 3.520

2.  Carrier detection in ornithine transcarbamylase deficiency.

Authors:  E A Haan; D M Danks; A Grimes; N J Hoogenraad
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

  2 in total

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