230 related articles for article (PubMed ID: 5438972)
1. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].
Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972
[No Abstract] [Full Text] [Related]
2. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies].
Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971
[No Abstract] [Full Text] [Related]
3. Arginase deficiency in Macaca fascicularis. I. Arginase activity and arginine concentration in erythrocytes and liver.
Shih VE; Jones TC; Levy HL; Madigan PM
Pediatr Res; 1972 Jun; 6(6):548-51. PubMed ID: 4625814
[No Abstract] [Full Text] [Related]
4. Hyperargininemia with arginase deficiency.
Cederbaum SD; Shaw KN; Spector EB; Verity MA; Snodgrass PJ; Sugarman GI
Pediatr Res; 1979 Jul; 13(7):827-33. PubMed ID: 481955
[No Abstract] [Full Text] [Related]
5. Use of enzyme-loaded erythrocytes in in-vitro correction of arginase-deficient erythrocytes in familial hyperargininemia.
Adriaenssens K; Karcher D; Lowenthal A; Terheggen HG
Clin Chem; 1976 Mar; 22(3):323-6. PubMed ID: 1253407
[TBL] [Abstract][Full Text] [Related]
6. Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia.
Vockley JG; Tabor DE; Kern RM; Goodman BK; Wissmann PB; Kang DS; Grody WW; Cederbaum SD
Hum Mutat; 1994; 4(2):150-4. PubMed ID: 7981719
[No Abstract] [Full Text] [Related]
7. Ammonia metabolism in a family affected by hyperargininemia.
Qureshi IA; Letarte J; Ouellet R; Lelièvre M; Laberge C
Diabete Metab; 1981 Mar; 7(1):5-11. PubMed ID: 7238975
[TBL] [Abstract][Full Text] [Related]
8. Liver fibrosis in arginase deficiency.
Jordá A; Portolés M; Rubio V; Capdevila A; Vilas J; García-Piño J
Arch Pathol Lab Med; 1987 Aug; 111(8):691-2. PubMed ID: 3632278
[No Abstract] [Full Text] [Related]
9. Arginase and free amino acids in hyperargininemia: leukocyte arginine as a diagnostic parameter for heterozygotes.
Marescau B; Pintens J; Lowenthal A; Terheggen HG; Adriaenssens K
J Clin Chem Clin Biochem; 1979 Apr; 17(4):211-7. PubMed ID: 438730
[TBL] [Abstract][Full Text] [Related]
10. Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities.
Sogawa H; Oyanagi K; Nakao T
Pediatr Res; 1977 Sep; 11(9 Pt 1):949-53. PubMed ID: 904980
[No Abstract] [Full Text] [Related]
11. Human hyperargininemia: a mutation not expressed in skin fibroblasts?
Van Elsen AF; Leroy JG
Am J Hum Genet; 1977 Jul; 29(4):350-5. PubMed ID: 879168
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis.
Korman SH; Gutman A; Stemmer E; Kay BS; Ben-Neriah Z; Zeigler M
Prenat Diagn; 2004 Nov; 24(11):857-60. PubMed ID: 15565656
[TBL] [Abstract][Full Text] [Related]
13. Argininemia.
Snyderman SE; Sansaricq C; Chen WJ; Norton PM; Phansalkar SV
J Pediatr; 1977 Apr; 90(4):563-8. PubMed ID: 839367
[TBL] [Abstract][Full Text] [Related]
14. Familial hyperargininemia.
Terheggen HG; Lavinha F; Colombo JP; Van Sande M; Lowenthal A
J Genet Hum; 1972 Mar; 20(1):69-84. PubMed ID: 4643877
[No Abstract] [Full Text] [Related]
15. Clinical and biochemical findings in argininemia.
Terheggen HG; Lowenthal A; Colombo JP
Adv Exp Med Biol; 1982; 153():111-9. PubMed ID: 7164891
[No Abstract] [Full Text] [Related]
16. Hyperargininemia, epilepsy and the metabolism of guanidino compounds.
Wiechert P; Marescau B; De Deyn PP; Lowenthal A
Padiatr Grenzgeb; 1989; 28(2):101-6. PubMed ID: 2657590
[TBL] [Abstract][Full Text] [Related]
17. Absence of erythrocyte arginase protein in Japanese patients with hyperargininemia.
Hayakawa C; Aono S; Keino H; Mizutani N; Watanabe K; Ikemoto M; Totani M; Murachi T; Kashiwamata S
Eur J Pediatr; 1991 Sep; 150(11):800-3. PubMed ID: 1959545
[TBL] [Abstract][Full Text] [Related]
18. Arginase deficiency in multiple tissues in argininemia.
Michels VV; Beaudet AL
Clin Genet; 1978 Jan; 13(1):61-7. PubMed ID: 624188
[TBL] [Abstract][Full Text] [Related]
19. A new case of arginase deficiency in a Spanish male.
Jordá A; Rubio V; Portolés M; Vilas J; García-Piño J
J Inherit Metab Dis; 1986; 9(4):393-7. PubMed ID: 3104676
[TBL] [Abstract][Full Text] [Related]
20. Arginase deficiency in two brothers.
Candito M; Bebin B; Vianey-Saban C; Rabier D; Bekri S; Sebag F; Chambon P; Kamoun P
J Inherit Metab Dis; 1993; 16(6):1054-6. PubMed ID: 8127062
[No Abstract] [Full Text] [Related]
[Next] [New Search]