167 related articles for article (PubMed ID: 7981719)
1. 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]
2. Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemia.
Cardoso ML; Martins E; Vasconcelos R; Vilarinho L; Rocha J
Hum Mutat; 1999 Oct; 14(4):355-6. PubMed ID: 10502833
[TBL] [Abstract][Full Text] [Related]
3. Molecular basis of argininemia. Identification of two discrete frame-shift deletions in the liver-type arginase gene.
Haraguchi Y; Aparicio JM; Takiguchi M; Akaboshi I; Yoshino M; Mori M; Matsuda I
J Clin Invest; 1990 Jul; 86(1):347-50. PubMed ID: 2365823
[TBL] [Abstract][Full Text] [Related]
4. Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase.
Ash DE; Scolnick LR; Kanyo ZF; Vockley JG; Cederbaum SD; Christianson DW
Mol Genet Metab; 1998 Aug; 64(4):243-9. PubMed ID: 9758714
[TBL] [Abstract][Full Text] [Related]
5. [Hyperargininemia. Clinical aspects and molecular basis of the defect].
Konarska L
Pediatr Pol; 1987 Apr; 62(4):261-72. PubMed ID: 3670917
[No Abstract] [Full Text] [Related]
6. [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]
7. 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]
8. The human arginases and arginase deficiency.
Iyer R; Jenkinson CP; Vockley JG; Kern RM; Grody WW; Cederbaum S
J Inherit Metab Dis; 1998; 21 Suppl 1():86-100. PubMed ID: 9686347
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Molecular basis of phenotypic variation in patients with argininemia.
Uchino T; Snyderman SE; Lambert M; Qureshi IA; Shapira SK; Sansaricq C; Smit LM; Jakobs C; Matsuda I
Hum Genet; 1995 Sep; 96(3):255-60. PubMed ID: 7649538
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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]
15. 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]
16. 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]
17. Immunologic studies of arginase in tissues of normal human adult and arginase-deficient patients.
Spector EB; Rice SC; Cederbaum SD
Pediatr Res; 1983 Dec; 17(12):941-4. PubMed ID: 6419196
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. [Argininemia (arginase deficiency)].
Haraguchi Y; Mori M
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):514-7. PubMed ID: 2908396
[No Abstract] [Full Text] [Related]
[Next] [New Search]
