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11 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. Hyperammonaemia. A new instance of an inborn enzymatic defect of the biosynthesis of urea.

Authors: A RUSSELL; B LEVIN; V G OBERHOLZER; L SINCLAIR
Journal: Lancet Date: 1962-10-06 Impact factor: 79.321

3. Pathogenesis and management of hepatic coma.

Authors: S SHERLOCK
Journal: Am J Med Date: 1958-05 Impact factor: 4.965

4. Episodic stupor associated with an Eck fistula in the human with particular reference to the metabolism of ammonia.

Authors: W V McDERMOTT; R D ADAMS
Journal: J Clin Invest Date: 1954-01 Impact factor: 14.808

5. Fructosaemia. Observations on seven cases.

Authors: B Levin; G J Snodgrass; V G Oberholzer; E A Burgess; R H Dobbs
Journal: Am J Med Date: 1968-12 Impact factor: 4.965

6. 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

7. 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

8. Arginosuccine aciduria.

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

9. Treatment of hyperammonemia.

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

10. Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients.

Authors: M Kekomäki; J K Visakorpi; J Perheentupa; L Saxén
Journal: Acta Paediatr Scand Date: 1967-11

19 in total

1. 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

2. 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

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

Authors: T Palmer; V G Oberholzer; E A Burgess; L J Butler; B Levin
Journal: Arch Dis Child Date: 1974-06 Impact factor: 3.791

4. 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

5. Carbamylphosphate synthetase deficiency in an infant with severe cerebral damage.

Authors: F A Hommes; C J De Groot; C W Wilmink; J H Jonxis
Journal: Arch Dis Child Date: 1969-12 Impact factor: 3.791

6. Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.

Authors: U Wendel; J Wieland; H J Bremer; C Bachmann
Journal: Eur J Pediatr Date: 1989-01 Impact factor: 3.183

7. Decreased hyperammonaemia and orotic aciduria due to inactivation of ornithine aminotransferase in mice with a hereditary abnormal ornithine carbamoyltransferase.

Authors: N Seiler; C Grauffel; G Daune-Anglard; S Sarhan; B Knödgen
Journal: J Inherit Metab Dis Date: 1994 Impact factor: 4.982

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