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14 in total

1. Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver.

Authors: G W BROWN; P P COHEN
Journal: J Biol Chem Date: 1959-07 Impact factor: 5.157

2. The estimation of plasma ammonia by ion exchange.

Authors: J C FENTON
Journal: Clin Chim Acta Date: 1962-03 Impact factor: 3.786

3. A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

Authors: J D ALLAN; D C CUSWORTH; C E DENT; V K WILSON
Journal: Lancet Date: 1958-01-25 Impact factor: 79.321

4. The free amino acids of human blood plasma.

Authors: W H STEIN; S MOORE
Journal: J Biol Chem Date: 1954-12 Impact factor: 5.157

5. Argininosuccinic aciduria, an inborn error of amino acid metabolism.

Authors: B LEVIN; H M MACKAY; V G OBERHOLZER
Journal: Arch Dis Child Date: 1961-12 Impact factor: 3.791

6. L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance.

Authors: W Bürgi; R Richterich; J P Colombo
Journal: Nature Date: 1966-08-20 Impact factor: 49.962

7. 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

8. Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism.

Authors: J Perheentupa; J K Visakorpi
Journal: Lancet Date: 1965-10-23 Impact factor: 79.321

9. Arginosuccine aciduria.

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

10. Treatment of hyperammonemia.

Authors: B Levin; A Russell
Journal: Am J Dis Child Date: 1967-01

23 in total

1. Ornithine transcarbamylase deficiency: a case with a truncated enzyme precursor and a case with undetectable mRNA activity.

Authors: H Kodama; A Ohtake; M Mori; I Okabe; M Tatibana; S Kamoshita
Journal: J Inherit Metab Dis Date: 1986 Impact factor: 4.982

2. Undiagnosed Partial Ornithine Transcarbamylase Deficiency Presenting Postoperatively as Agitated Delirium.

Authors: E D Goldstein; R Cannistraro; P S Atwal; J F Meschia
Journal: Neurohospitalist Date: 2017-09-12

3. Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activity.

Authors: S Mantagos; S Tsagaraki; E A Burgess; V Oberholzer; T Palmer; J Sacks; S Baibas; T Valaes
Journal: Arch Dis Child Date: 1978-03 Impact factor: 3.791

4. X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase.

Authors: F C Ricciuti; T D Gelehrter; L E Rosenberg
Journal: Am J Hum Genet Date: 1976-07 Impact factor: 11.025

5. Hyperammonemia through deficiency of ornithine carbamyl transferase.

Authors: J P Farriaux; J L Dhondt; L Cathelineau; J Ratel; G Fontaine
Journal: Z Kinderheilkd Date: 1974

6. [Developing mechanism of the adverse effects of L-asparaginase and their control].

Authors: J Kodama; K Higashino; S Kobayashi; K Izumi; M Satani
Journal: Blut Date: 1974-01

7. Neuropathology of ornithine carbamyl transferase deficiency.

Authors: M Kornfeld; B M Woodfin; L Papile; L E Davis; L R Bernard
Journal: Acta Neuropathol Date: 1985 Impact factor: 17.088

8. Citrulline synthesis in rat tissues and liver content of carbamoyl phosphate and ornithine.

Authors: L Raijman
Journal: Biochem J Date: 1974-02 Impact factor: 3.857

9. X-linked dominant inherited diseases with lethality in hemizygous males.

Authors: R Wettke-Schäfer; G Kantner
Journal: Hum Genet Date: 1983 Impact factor: 4.132

10. Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.

Authors: W Holzgreve; M S Golbus
Journal: Am J Hum Genet Date: 1984-03 Impact factor: 11.025