162 related articles for article (PubMed ID: 4446691)
1. Hyperammonemia through deficiency of ornithine carbamyl transferase.
Farriaux JP; Dhondt JL; Cathelineau L; Ratel J; Fontaine G
Z Kinderheilkd; 1974; 118(3):231-47. PubMed ID: 4446691
[No Abstract] [Full Text] [Related]
2. Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency.
van der Heiden C; Bakker HD; Desplanque J; Brink M; de Bree PK; Wadman SK
Eur J Pediatr; 1978 Jul; 128(4):261-72. PubMed ID: 668733
[TBL] [Abstract][Full Text] [Related]
3. Ornithine transcarbamylase deficiency--a cause of bizarre behavior in a man.
DiMagno EP; Lowe JE; Snodgrass PJ; Jones JD
N Engl J Med; 1986 Sep; 315(12):744-7. PubMed ID: 3748082
[No Abstract] [Full Text] [Related]
4. Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency.
Hou JW; Wang TR
J Formos Med Assoc; 1996 Feb; 95(2):144-7. PubMed ID: 9064003
[TBL] [Abstract][Full Text] [Related]
5. Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males.
Campbell AG; Rosenberg LE; Snodgrass PJ; Nuzum CT
N Engl J Med; 1973 Jan; 288(1):1-6. PubMed ID: 4681895
[No Abstract] [Full Text] [Related]
6. Ornithine transcarbamylase deficiency in a boy with normal development.
Yudkoff M; Yang W; Snodgrass PJ; Segal S
J Pediatr; 1980 Mar; 96(3 Pt 1):441-3. PubMed ID: 7188954
[No Abstract] [Full Text] [Related]
7. [Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy].
Saudubray JM; Cathelineau L; Charpentier C; Boisse J; Allaneau C; Le Bont H; Lesage B
Arch Fr Pediatr; 1973 Jan; 30(1):15-27. PubMed ID: 4721585
[No Abstract] [Full Text] [Related]
8. Sodium valproate and ornithine carbamyl transferase deficiency.
Tripp JH; Hargreaves T; Anthony PP; Searle JF; Miller P; Leonard JV; Patrick AD; Oberholzer VG
Lancet; 1981 May; 1(8230):1165-6. PubMed ID: 6112522
[No Abstract] [Full Text] [Related]
9. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R
Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461
[No Abstract] [Full Text] [Related]
10. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
Pridmore CL; Clarke JT; Blaser S
J Child Neurol; 1995 Sep; 10(5):369-74. PubMed ID: 7499756
[TBL] [Abstract][Full Text] [Related]
11. A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet.
Gjessing LR; Lunde HA; Undrum T; Broch H; Alme A; Lie SO
J Inherit Metab Dis; 1986; 9(2):186-92. PubMed ID: 3091924
[TBL] [Abstract][Full Text] [Related]
12. Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.
Kendall BE; Kingsley DP; Leonard JV; Lingam S; Oberholzer VG
J Neurol Neurosurg Psychiatry; 1983 Jan; 46(1):28-34. PubMed ID: 6842197
[TBL] [Abstract][Full Text] [Related]
13. [Congenital hyperammoniemia caused by ornithine carbamoyl-transferase and carbamyl phosphate synthetase deficiency].
Salle B; Levin B; Longin B; Richard P; Andre M; Gauthier J
Arch Fr Pediatr; 1972 May; 29(5):493-504. PubMed ID: 4655647
[No Abstract] [Full Text] [Related]
14. Failure of protein loading tests to identify heterozygosity for ornithine carbamoyltransferase deficiency.
Becroft DM; Barry DM; Webster DR; Simmonds HA
J Inherit Metab Dis; 1984; 7(4):157-9. PubMed ID: 6441862
[TBL] [Abstract][Full Text] [Related]
15. Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.
Wendel U; Wieland J; Bremer HJ; Bachmann C
Eur J Pediatr; 1989 Jan; 148(4):349-52. PubMed ID: 2707281
[TBL] [Abstract][Full Text] [Related]
16. Orotic acid in urine and hyperammonemia.
Bachmann C; Colombo JP
Adv Exp Med Biol; 1982; 153():313-9. PubMed ID: 7164906
[No Abstract] [Full Text] [Related]
17. [Congenital deficiency of ornithine transcarbamylase. Description of 2 clinical cases].
D'Eufemia P; Corrado G; Sabetta G; Castro M; Martino F; Cantani A; Ruberto U
Minerva Pediatr; 1983 Mar; 35(5):219-24. PubMed ID: 6343831
[No Abstract] [Full Text] [Related]
18. Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium.
Oizumi J; Ng WG; Koch R; Shaw KN; Sweetman L; Velazquez A; Donnell GN
Clin Genet; 1984 Jun; 25(6):538-42. PubMed ID: 6733950
[TBL] [Abstract][Full Text] [Related]
19. Hereditary ornithine transcarbamylase deficiency. Report of two male cases with residual enzymatic activity.
Saudubray JM; Cathelineau L; Laugier JM; Charpentier C; Lejeune JA; Mozziconacci P
Acta Paediatr Scand; 1975 May; 64(3):464-72. PubMed ID: 168725
[TBL] [Abstract][Full Text] [Related]
20. [Neonatal hyperammonemia due to ornithine transcarbamylase deficiency (author's transl)].
del Valle JA; Urbón A; García MJ; Cuadrado P; Ugarte M
An Esp Pediatr; 1982 May; 16(5):416-20. PubMed ID: 7114619
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
