BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 6434849)

  • 1. Pyruvate carboxylase deficiency.
    Bartlett K; Ghneim HK; Stirk JH; Dale G; Alberti KG
    J Inherit Metab Dis; 1984; 7 Suppl 1():74-8. PubMed ID: 6434849
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lactic acidaemia.
    Robinson BH; Sherwood WG
    J Inherit Metab Dis; 1984; 7 Suppl 1():69-73. PubMed ID: 6434848
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylase.
    Van Biervliet JP; Duran M; Wadman SK; Koster JF; van Rossum A
    J Inherit Metab Dis; 1980; 2(1):15-8. PubMed ID: 6796755
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defective biotin absorption in multiple carboxylase deficiency.
    Munnich A; Saudubray JM; Carré G; Coudé FX; Ogier H; Charpentier C; Frézal J
    Lancet; 1981 Aug; 2(8240):263. PubMed ID: 6114319
    [No Abstract]   [Full Text] [Related]  

  • 5. [Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency].
    Merinero Cortés B; del Valle Martínez J; Pérez-Cerdá Silvestre C; García Muñoz MJ; Cortés Coto MT; García Aparicio J; Sáez Pérez E; Ugarte Pérez M
    An Esp Pediatr; 1988 Jul; 29(1):57-60. PubMed ID: 3142324
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings.
    Saudubray JM; Marsac C; Cathelineau CL; Besson Leaud M; Leroux JP
    Acta Paediatr Scand; 1976 Nov; 65(6):717-24. PubMed ID: 826106
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Organic aciduria in late-onset biotin-responsive multiple carboxylase deficiency.
    Erasmus C; Mienie LJ; Reinecke CJ; Wadman SK
    J Inherit Metab Dis; 1985; 8 Suppl 2():105-6. PubMed ID: 3930851
    [No Abstract]   [Full Text] [Related]  

  • 8. Lactic acidosis in paediatrics: clinical and laboratory evaluation.
    Stern HJ
    Ann Clin Biochem; 1994 Sep; 31 ( Pt 5)():410-9. PubMed ID: 7832568
    [No Abstract]   [Full Text] [Related]  

  • 9. Prenatal treatment of biotin responsive multiple carboxylase deficiency.
    Packman S; Cowan MJ; Golbus MS; Caswell NM; Sweetman L; Burri BJ; Nyhan WL; Baker H
    Lancet; 1982 Jun; 1(8287):1435-8. PubMed ID: 6123722
    [No Abstract]   [Full Text] [Related]  

  • 10. [A case of congenital lactic acidosis caused by deficiency of pyruvate dehydrogenase].
    Salti R; Galluzzi F; Liguri GF; Marianelli L; Zammarchi E; La Cauza C
    Minerva Pediatr; 1979 Nov; 31(21):1539-46. PubMed ID: 118331
    [No Abstract]   [Full Text] [Related]  

  • 11. The measurement of propionyl-CoA carboxylase and pyruvate carboxylase activity in hair roots: its use in the diagnosis of inherited biotin-dependent enzyme deficiencies.
    Wolf B; Raetz H
    Clin Chim Acta; 1983 May; 130(1):25-30. PubMed ID: 6851181
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and biochemical findings on a child with multiple biotin-responsive carboxylase deficiencies.
    Narisawa K; Arai N; Igarashi Y; Satoh T; Tada K; Hirooka Y
    J Inherit Metab Dis; 1982; 5(2):67-8. PubMed ID: 6133032
    [No Abstract]   [Full Text] [Related]  

  • 13. Pyruvate-carboxylase deficiency with urea cycle impairment.
    Greter J; Gustafsson J; Holme E
    Acta Paediatr Scand; 1985 Nov; 74(6):982-6. PubMed ID: 3937431
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis.
    Robinson BH; Taylor J; Sherwood WG
    Pediatr Res; 1980 Aug; 14(8):956-62. PubMed ID: 6775276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.
    Oizumi J; Donnell GN; Ng WG; Mulivor RA; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1984; 38(1):80. PubMed ID: 6705569
    [No Abstract]   [Full Text] [Related]  

  • 16. Report of a patient with severe, chronic lactic acidaemia and pyruvate carboxylase deficiency.
    Van Biervliet JP; Bruinvis L; van der Heiden C; Ketting D; Wadman SK; Willemse JL; Monnens LA
    Dev Med Child Neurol; 1977 Jun; 19(3):392-401. PubMed ID: 407120
    [No Abstract]   [Full Text] [Related]  

  • 17. Organic acids in urine of patients with congenital lactic acidoses: an aid to differential diagnosis.
    Chalmers RA
    J Inherit Metab Dis; 1984; 7 Suppl 1():79-89. PubMed ID: 6434850
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lactic acidosis due to pyruvate carboxylase deficiency.
    Haworth JC; Robinson BH; Perry TL
    J Inherit Metab Dis; 1981; 4(2):57-8. PubMed ID: 6790846
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biochemical and histologic pathology in an infant with cross-reacting material (negative) pyruvate carboxylase deficiency.
    Wong LT; Davidson AG; Applegarth DA; Dimmick JE; Norman MG; Toone JR; Pirie G; Wong J
    Pediatr Res; 1986 Mar; 20(3):274-9. PubMed ID: 3085060
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of pyruvate carboxylase deficiency.
    Robinson BH; Toone JR; Benedict RP; Dimmick JE; Oei J; Applegarth DA
    Prenat Diagn; 1985; 5(1):67-71. PubMed ID: 3919380
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.