143 related articles for article (PubMed ID: 6076999)
1. Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients.
Kekomäki M; Visakorpi JK; Perheentupa J; Saxén L
Acta Paediatr Scand; 1967 Nov; 56(6):617-30. PubMed ID: 6076999
[No Abstract] [Full Text] [Related]
2. Lysinuric protein intolerance.
Simell O; Perheentupa J; Rapola J; Visakorpi JK; Eskelin LE
Am J Med; 1975 Aug; 59(2):229-40. PubMed ID: 1155480
[TBL] [Abstract][Full Text] [Related]
3. Enzymes of urea synthesis in familial protein intolerance with deficient transport of basic amino acids.
Kekomäki M; Räihä NC; Perheentupa J
Acta Paediatr Scand; 1967 Nov; 56(6):631-6. PubMed ID: 6077000
[No Abstract] [Full Text] [Related]
4. Hyperdibasicaminoaciduria and hyperammonemia in familial protein intolerance.
Kato T; Tanaka E; Horisawa S
Am J Dis Child; 1976 Dec; 130(12):1340-4. PubMed ID: 998577
[TBL] [Abstract][Full Text] [Related]
5. Familial protein intolerance with deficient transport of basic amino acids. Report on an adult patient with chronic hyperammonemia.
Kekomäki M; Toivakka E; Häkkinen V; Salaspuro M
Acta Med Scand; 1968 Apr; 183(4):357-9. PubMed ID: 5666624
[No Abstract] [Full Text] [Related]
6. Citrullinemia: investigation and treatment over a four-year period.
Buist NR; Kennaway NG; Hepburn CA; Strandholm JJ; Ramberg DA
J Pediatr; 1974 Aug; 85(2):208-14. PubMed ID: 4842795
[No Abstract] [Full Text] [Related]
7. Familial protein intolerance. Possible nature of enzyme defect.
Malmquist J; Jagenburg R; Lindstedt G
N Engl J Med; 1971 May; 284(18):997-1002. PubMed ID: 5553484
[No Abstract] [Full Text] [Related]
8. [DISEASES CAUSED BY METABOLIC DISORDER OF THE KREBS-HENSELEIT CYCLE].
LEDERER J
Scalpel (Brux); 1964 Mar; 117():263-8. PubMed ID: 14142236
[No Abstract] [Full Text] [Related]
9. Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism.
Perheentupa J; Visakorpi JK
Lancet; 1965 Oct; 2(7417):813-6. PubMed ID: 4158034
[No Abstract] [Full Text] [Related]
10. Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.
Oyanagi K; Miura R; Yamanouchi T
J Pediatr; 1970 Aug; 77(2):259-66. PubMed ID: 5431208
[No Abstract] [Full Text] [Related]
11. 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]
12. Lysinuric protein intolerance presenting deficiency of argininosuccinate synthetase.
Ono N; Kishida K; Tokumoto K; Watanabe M; Shimada Y; Yoshinaga J; Fujii M
Intern Med; 1992 Jan; 31(1):55-9. PubMed ID: 1568044
[TBL] [Abstract][Full Text] [Related]
13. Severe neonatal citrullinaemia.
Danks DM; Tippett P; Zentner G
Arch Dis Child; 1974 Jul; 49(7):579-81. PubMed ID: 4854268
[No Abstract] [Full Text] [Related]
14. Treatment of hyperammonemia.
Levin B; Russell A
Am J Dis Child; 1967 Jan; 113(1):142-5. PubMed ID: 6015891
[No Abstract] [Full Text] [Related]
15. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
Brusilow SW
J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918
[TBL] [Abstract][Full Text] [Related]
16. [A family with pyroglutamic aciduria (author's transl)].
Porath U; Schreier K
Dtsch Med Wochenschr; 1978 Jun; 103(22):939-42. PubMed ID: 657978
[No Abstract] [Full Text] [Related]
17. [Physiological and pathological aminoacidurias].
Brodehl J
Monatsschr Kinderheilkd (1902); 1973 May; 121(5):190-200. PubMed ID: 4713389
[No Abstract] [Full Text] [Related]
18. The congenital hyperammonemic syndrome.
Berenberg W; Kang ES
Dev Med Child Neurol; 1971 Jun; 13(3):355-61. PubMed ID: 5093296
[No Abstract] [Full Text] [Related]
19. Cystathioninuria and renal iminoglycinuria in a pedigree.
Whelan DT; Scriver CR
N Engl J Med; 1968 Apr; 278(17):924-7. PubMed ID: 5644557
[No Abstract] [Full Text] [Related]
20. [Indications of renal and intestinal amino acid malabsorption in Lowe's syndrome].
Colombo JP
Schweiz Med Wochenschr; 1971 Jul; 101(26):968-72. PubMed ID: 5143472
[No Abstract] [Full Text] [Related]
[Next] [New Search]
