These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 5438972)

  • 21. [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]  

  • 22. Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissues.
    Endres W; Schaller R; Shin YS
    J Inherit Metab Dis; 1984; 7(1):8. PubMed ID: 6429443
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Hyperargininemia.
    Cederbaum SD; Shaw KN; Valente M
    J Pediatr; 1977 Apr; 90(4):569-73. PubMed ID: 839368
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Intravenous loading with arginine-hydrochloride and ornithine-aspartate in siblings of two families, presenting a familial neurological syndrome associated with cystinuria.
    Strauven T; Mardens Y; Clara R; Terheggen H
    Biomedicine; 1976 Jun; 24(3):191-9. PubMed ID: 990372
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Lethal familial neonatal ketotic hyperammonemia].
    Pauli A; Huguet J; Rollet M; Cousin J; Farriaux JP; Fournier A; Navarro J; Cathelineau L; Aymard P; Saudubray JM; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):699-712. PubMed ID: 4644460
    [No Abstract]   [Full Text] [Related]  

  • 29. Arginase deficiency presenting with convulsions.
    Patel JS; van't Hoff WV; Leonard JV
    J Inherit Metab Dis; 1994; 17(2):254. PubMed ID: 7967487
    [No Abstract]   [Full Text] [Related]  

  • 30. A new French-Canadian family affected by hyperargininaemia.
    Qureshi IA; Letarte J; Ouellet R; Larochelle J; Lemieux B
    J Inherit Metab Dis; 1983; 6(4):179-82. PubMed ID: 6422160
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Further investigations in hyperargininemia.
    Van Sande M; Terheggen HG; Colombo JP; Lowenthal A; Rogers S; Schwenk A
    Monogr Hum Genet; 1972; 6():143. PubMed ID: 4663887
    [No Abstract]   [Full Text] [Related]  

  • 32. [Argininemia (arginase deficiency)].
    Haraguchi Y; Mori M
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):514-7. PubMed ID: 2908396
    [No Abstract]   [Full Text] [Related]  

  • 33. [Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies].
    Thiriar MJ; Szliwowski HB; Vis HL
    Acta Neurol Psychiatr Belg; 1968 Mar; 68(3):216-27. PubMed ID: 4972603
    [No Abstract]   [Full Text] [Related]  

  • 34. Hyperdibasicaminoaciduria in a mentally retarded homozygote with a peculiar response to phenothiazines.
    Kihara H; Valente M; Porter MT; Fluharty AL
    Pediatrics; 1973 Feb; 51(2):223-9. PubMed ID: 4144453
    [No Abstract]   [Full Text] [Related]  

  • 35. Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy.
    Marescau B; De Deyn PP; Lowenthal A; Qureshi IA; Antonozzi I; Bachmann C; Cederbaum SD; Cerone R; Chamoles N; Colombo JP
    Pediatr Res; 1990 Mar; 27(3):297-303. PubMed ID: 1690873
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Special course of arginine succinic acid disease].
    Porath U; Liebler G; Schreier K
    Arch Kinderheilkd; 1969 Sep; 179(3):283-8. PubMed ID: 5356533
    [No Abstract]   [Full Text] [Related]  

  • 37. [Physiopathological considerations on the limits of detection of certain metabolic syndromes of the cystinuria-cystinosis type. Possibilities of rapid diagnosis].
    Pâtea P; Tănase-Mogos I; Ciortoloman H; Petrescu L; Ciucă C; Orăşeanu D; Jemna M; Meila P
    Physiologie; 1980; 17(2):113-20. PubMed ID: 6770383
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Hyperargininemia: the rat as a model for the human disease and the comparative response to enzyme replacement therapy with free arginase and arginase-loaded erythrocytes in vivo.
    Adriaenssens K; Karcher D; Marescau B; Van Broeckhoven C; Lowenthal A; Terheggen HC
    Int J Biochem; 1984; 16(7):779-86. PubMed ID: 6468738
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Type I hyperprolinemia. Study of a familial case].
    Fontaine G; Farriaux JP; Dautrevaux M
    Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.