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Journal Abstract Search

179 related items for PubMed ID: 533302

  • 1. Treatment of a neonate with propionic acidaemia and severe hyperammonaemia by peritoneal dialysis.
    Robert MF, Schultz DJ, Wolf B, Cochran WD, Schwartz AL.
    Arch Dis Child; 1979 Dec; 54(12):962-5. PubMed ID: 533302
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  • 3. The glutamine paradox in a neonate with propionic acidaemia and severe hyperammonaemia.
    Ierardi-Curto L, Kaplan P, Saitta S, Mazur A, Berry GT.
    J Inherit Metab Dis; 2000 Feb; 23(1):85-6. PubMed ID: 10682312
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  • 4. Efficacy of peritoneal dialysis in neonates presenting with hyperammonaemia due to urea cycle defects and organic acidaemia.
    Celik M, Akdeniz O, Ozgun N.
    Nephrology (Carlton); 2019 Mar; 24(3):330-335. PubMed ID: 29356227
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  • 6. Absence of acidosis in the initial presentation of propionic acidaemia.
    Walter JH, Wraith JE, Cleary MA.
    Arch Dis Child Fetal Neonatal Ed; 1995 May; 72(3):F197-9. PubMed ID: 7796239
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  • 10. A simple isotopic technique for assessing vitamin responsiveness in vivo in propionic acidaemia.
    Thompson GN, Bresson JL, Bonnefont JP, Walter JH, Read MA, Saudubray JM, Leonard JV, Halliday D.
    J Inherit Metab Dis; 1990 May; 13(3):349-51. PubMed ID: 2122099
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  • 11. [Therapy of hyperammonemia in carbamyl phosphate synthase deficiency with peritoneal dialysis and venovenous hemofiltration].
    Lettgen B, Bonzel KE, Colombo JP, Fuchs B, Kordass U, Wendel K, Rascher W.
    Monatsschr Kinderheilkd; 1991 Sep; 139(9):612-7. PubMed ID: 1745252
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  • 13. An unusual late-onset case of propionic acidaemia: biochemical investigations, neuroradiological findings and mutation analysis.
    Pérez-Cerdá C, Merinero B, Martí M, Cabrera JC, Peña L, García MJ, Gangoiti J, Sanz P, Rodríguez-Pombo P, Hoenicka J, Richard E, Muro S, Ugarte M.
    Eur J Pediatr; 1998 Jan; 157(1):50-2. PubMed ID: 9461363
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  • 14. Propionic acidemia with severe hyperammonemia and defective glycine metabolism.
    Shafai T, Sweetman L, Weyler W, Goodman SI, Fennessey PV, Nyhan WL.
    J Pediatr; 1978 Jan; 92(1):84-6. PubMed ID: 619088
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  • 15. [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
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  • 16. 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 May; 5(2):121-4. PubMed ID: 6820422
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  • 17. Late onset type of propionic acidaemia: case report and biochemical studies.
    Merinero B, DelValle JA, Jiménez A, Garcia MJ, Ugarte M, Solaguren R, López O, Condado I.
    J Inherit Metab Dis; 1981 May; 4(2):71-2. PubMed ID: 6790853
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  • 18. Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects.
    Corbeel L, Tada K, Colombo JP, Eeckels R, Eggermont E, Jaeken J, Den Tandt W, Harvengt L, Delhaye J, Deloecker W.
    Arch Dis Child; 1975 Feb; 50(2):103-9. PubMed ID: 236734
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  • 19. Erythematous skin lesions and partial deficiency of 3-methylcrotonyl-CoA carboxylase in peripheral lymphocytes in a patient with propionic acidaemia.
    Yoshino M, Aramaki S, Yamashita F, Sato K, Inoue Y, Kuhara T, Matsumoto I.
    J Inherit Metab Dis; 1991 Feb; 14(5):839-40. PubMed ID: 1779636
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  • 20. Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria.
    Purkiss P, Chalmers RA, Borud O.
    J Inherit Metab Dis; 1980 Feb; 3(3):85-6. PubMed ID: 6775144
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