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12 in total

1. ARGININOSUCCINIC ACIDURIA. ARGININOSUCCINASE AND ARGINASE IN HUMAN BLOOD CELLS.

Authors: S TOMLINSON; R G WESTALL
Journal: Clin Sci Date: 1964-04 Impact factor: 6.124

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. The measurement of ammonia in whole blood, erythrocytes, and plasma.

Authors: D SELIGSON; K HIRAHARA
Journal: J Lab Clin Med Date: 1957-06

4. Kinetics of ammonia metabolism in vivo.

Authors: G D DUDA; P HANDLER
Journal: J Biol Chem Date: 1958-05 Impact factor: 5.157

5. Adaptive characteristics of urea cycle enzymes in the rat.

Authors: R T SCHIMKE
Journal: J Biol Chem Date: 1962-02 Impact factor: 5.157

6. Hereditary orotic aciduria. II. A urinary screening test.

Authors: L E Rogers; F S Porter
Journal: Pediatrics Date: 1968-09 Impact factor: 7.124

7. 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

8. 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

9. [Periodic stupor and ammonia intoxication in a child with anicteric subacute hepatitis].

Authors: J P Colombo; S Ungari; F Ferrazzini; R Richterich; E Rossi
Journal: Helv Paediatr Acta Date: 1967-08

10. [A micromethod for determining ornithine carbamoyltransferase (OCT) in blood and cerebrospinal fluid].

Authors: H WEBER
Journal: Klin Wochenschr Date: 1963-01-01

9 in total

1. 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

2. [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

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. Hair amino acids: normal values and results in metabolic errors.

Authors: M Van Sande
Journal: Arch Dis Child Date: 1970-10 Impact factor: 3.791

5. Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects.

Authors: L Corbeel; K Tada; J P Colombo; R Eeckels; E Eggermont; J Jaeken; W Den Tandt; L Harvengt; J Delhaye; W Deloecker
Journal: Arch Dis Child Date: 1975-02 Impact factor: 3.791

6. 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

7. 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

8. 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

9. Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant.

Authors: P MacLeod; S Mackenzie; C R Scriver
Journal: Can Med Assoc J Date: 1972-09-09 Impact factor: 8.262

9 in total