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Journal Abstract Search

164 related items for PubMed ID: 1133651

  • 21. [Hyperglycinemia in clinical-laboratory practice].
    Ciani F, Pasquini E, Ciardetti A, Donati MA, Zammarchi E.
    Pediatr Med Chir; 1997; 19(2):109-12. PubMed ID: 9312744
    [Abstract] [Full Text] [Related]

  • 22. [Blood propionic acid with hyperammonemic coma].
    Stöckler S, Kastner U, Pokits B, Müller W, Roscher A.
    Klin Padiatr; 1987; 199(5):348-50. PubMed ID: 3682709
    [Abstract] [Full Text] [Related]

  • 23. Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiency.
    DelValle JA, Merinero B, Jiménez A, García MJ, Ugarte M, Omeñaca F, Neustadt G, Quero J.
    J Inherit Metab Dis; 1982; 5(2):121-4. PubMed ID: 6820422
    [Abstract] [Full Text] [Related]

  • 24. A Rare Case of Propionic Acidemia in a Six Months Female Child.
    Irum S, Rehman A, Aamir M, Haroon ZH, Chaudhry N, Bibi A.
    J Coll Physicians Surg Pak; 2022 Aug; 32(8):S180-S182. PubMed ID: 36210688
    [Abstract] [Full Text] [Related]

  • 25. Propionic acidaemia presenting with pancytopaenia in infancy.
    Sweetman L, Nyhan WL, Cravens J, Zomer Y, Plunket DC.
    J Inherit Metab Dis; 1980 Aug; 2(3):65-9. PubMed ID: 6796762
    [Abstract] [Full Text] [Related]

  • 26. Propionic acidemia: unusual course with late onset and fatal outcome.
    Lücke T, Pérez-Cerdá C, Baumgartner M, Fowler B, Sander S, Sasse M, Scholl S, Ugarte M, Das AM.
    Metabolism; 2004 Jun; 53(6):809-10. PubMed ID: 15164333
    [Abstract] [Full Text] [Related]

  • 27. [Propionicacidemia. A report on two cases (author's transl)].
    Costil J, Debard A, Guilhaume A, Charpentier C, Pousset JL, Brissaud HE.
    Ann Pediatr (Paris); 1979 May; 26(5):283-8. PubMed ID: 555851
    [No Abstract] [Full Text] [Related]

  • 28. Inherited propionyl-Coa carboxylase deficiency in "ketotic hyperglycinemia".
    Hsia YE, Scully KJ, Rosenberg LE.
    J Clin Invest; 1971 Jan; 50(1):127-30. PubMed ID: 5101292
    [Abstract] [Full Text] [Related]

  • 29. Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome".
    Hillman RE, Keating JP.
    Pediatrics; 1974 Feb; 53(2):221-5. PubMed ID: 4812006
    [No Abstract] [Full Text] [Related]

  • 30. Importance of the single case.
    N Engl J Med; 1968 Jun 13; 278(24):1347. PubMed ID: 5648602
    [No Abstract] [Full Text] [Related]

  • 31. Effect of valine on propionate metabolism in control and hyperglycinemic fibroblasts and in rat liver.
    Revsin B, Lebowitz J, Morrow G.
    Pediatr Res; 1977 Jun 13; 11(6):749-53. PubMed ID: 17092
    [Abstract] [Full Text] [Related]

  • 32. Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria.
    Weyler W, Sweetman L, Maggio DC, Nyhan WL.
    Clin Chim Acta; 1977 May 02; 76(3):321-8. PubMed ID: 858206
    [Abstract] [Full Text] [Related]

  • 33. Mild form of methylmalonic aciduria misdiagnosed as propionic acidaemia during a ketotic crisis.
    de Almeida IT, Duran M, Silva MF, Portela R, Cabral A, Tasso T, Eusébio F, Silveira C.
    J Inherit Metab Dis; 1991 May 02; 14(2):259-62. PubMed ID: 1886409
    [No Abstract] [Full Text] [Related]

  • 34. Neurologic nonmetabolic presentation of propionic acidemia.
    Nyhan WL, Bay C, Beyer EW, Mazi M.
    Arch Neurol; 1999 Sep 02; 56(9):1143-7. PubMed ID: 10488817
    [Abstract] [Full Text] [Related]

  • 35. 3-hydroxypropionate: significance of -oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia.
    Ando T, Rasmussen K, Nyhan WL, Hull D.
    Proc Natl Acad Sci U S A; 1972 Oct 02; 69(10):2807-11. PubMed ID: 4507604
    [Abstract] [Full Text] [Related]

  • 36. Localisation of enzymic defect in propionicacidaemia.
    Gompertz D, Storrs CN, Bau DC, Peters TJ, Hughes EA.
    Lancet; 1970 May 30; 1(7657):1140-3. PubMed ID: 4192098
    [No Abstract] [Full Text] [Related]

  • 37. Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.
    Przyrembel H, Bremer HJ, Duran M, Bruinvis L, Ketting D, Wadman SK, Baumgartner R, Irle U, Bachmann C.
    Eur J Pediatr; 1979 Jan 18; 130(1):1-14. PubMed ID: 759179
    [Abstract] [Full Text] [Related]

  • 38. Propionic acidemia without acidemia: a case report.
    Ramachandran R, Pietz J.
    J Perinatol; 1995 Jan 18; 15(1):71-3. PubMed ID: 7650559
    [Abstract] [Full Text] [Related]

  • 39. A Rare Cause of Life-Threatening Ketoacidosis: Novel Compound Heterozygous OXCT1 Mutations Causing Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency.
    Kim YA, Kim SH, Cheon CK, Kim YM.
    Yonsei Med J; 2019 Mar 18; 60(3):308-311. PubMed ID: 30799594
    [Abstract] [Full Text] [Related]

  • 40. Beta-ketothiolase deficiency. A case report.
    Altintaş B, Teziç T, Coşkun T, Ozalp I, Kükner S, Kaya A.
    Turk J Pediatr; 1992 Mar 18; 34(1):43-6. PubMed ID: 1509529
    [Abstract] [Full Text] [Related]

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