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Journal Abstract Search

120 related items for PubMed ID: 5422739

  • 41. Parenteral nutrition in propionic and methylmalonic acidemia.
    Kahler SG, Millington DS, Cederbaum SD, Vargas J, Bond LD, Maltby DA, Gale DS, Roe CR.
    J Pediatr; 1989 Aug; 115(2):235-41. PubMed ID: 2502611
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  • 44. Hydroxylysinemia; a disorder due to a defect in the metabolism of free hydroxylysine.
    Goodman SI, Browder JA, Hiles RA, Miles ES.
    Biochem Med; 1972 Aug; 6(4):344-54. PubMed ID: 5048993
    [No Abstract] [Full Text] [Related]

  • 45. Dietary therapy in two patients with vitamin B12-unresponsive methylmalonic acidemia.
    Satoh T, Narisawa K, Igarashi Y, Saitoh T, Hayasaka K, Ichinohazama Y, Onodera H, Tada K, Oohara K.
    Eur J Pediatr; 1981 Feb; 135(3):305-12. PubMed ID: 7227387
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  • 46. Biochemical diagnosis and outcome of 2 years treatment in a patient with combined methylmalonic aciduria and homocystinuria.
    Bellini C, Cerone R, Bonacci W, Caruso U, Magliano CP, Serra G, Fowler B, Romano C.
    Eur J Pediatr; 1992 Nov; 151(11):818-20. PubMed ID: 1468456
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  • 47. [Study of a case of methylmalonic acidemia of neonatal onset. Therapeutic value of peritoneal dialysis. Discussion of vitamin B 12 sensitivity].
    Saudubray JM, Boisse J, Charpentier C, Lemonnier A, Mozziconacci P.
    Arch Fr Pediatr; 1972 Nov; 29(6):676-7. PubMed ID: 5078375
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  • 48. [A case of cobalamin-dependent methylmalonic acidemia. Biochemical aspects, diagnosis and possible treatment (author's transl)].
    Schuchmann L, Leupold D, Lehnert W.
    Monatsschr Kinderheilkd (1902); 1978 Apr; 126(4):179-83. PubMed ID: 651892
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  • 49. A guide to screening newborn infants for inborn errors of metabolism.
    Buist NR, Jhaveri BM.
    J Pediatr; 1973 Mar; 82(3):511-22. PubMed ID: 4266933
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  • 51. [Early detection of congenital metabolic anomalies].
    Thalhammer O.
    Klin Padiatr; 1973 Mar; 185(2):81-90. PubMed ID: 4576950
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  • 53. The occurrence of beta-hydroxy-n-valeric acid in a patient with propionic and methylmalonic acidemia.
    Stokke O, Jellum E, Eldjarn L, Schnitler R.
    Clin Chim Acta; 1973 May 30; 45(4):391-401. PubMed ID: 4730209
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  • 54. Age-Specific Cut-off Values of Amino Acids and Acylcarnitines for Diagnosis of Inborn Errors of Metabolism Using Liquid Chromatography Tandem Mass Spectrometry.
    Sarker SK, Islam MT, Biswas A, Bhuyan GS, Sultana R, Sultana N, Rakhshanda S, Begum MN, Rahat A, Yeasmin S, Khanam M, Saha AK, Noor FA, Sajib AA, Islam ABMMK, Qadri SK, Shahidullah M, Mannan MA, Muraduzzaman AKM, Shirin T, Rahman SM, Qadri SS, Saha N, Akhteruzzaman S, Qadri F, Mannoor K.
    Biomed Res Int; 2019 May 30; 2019():3460902. PubMed ID: 30723736
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  • 55. Screening tests and chromatography for the detection of inborn errors of metabolism.
    Stuber A.
    Clin Chim Acta; 1972 Feb 30; 36(2):309-13. PubMed ID: 5008795
    [No Abstract] [Full Text] [Related]

  • 56. Parenteral nutrition in propionic acidemia and methylmalonic acidemia.
    Walter JH, Leonard JV, Thompson GN, Halliday D.
    J Pediatr; 1990 Aug 30; 117(2 Pt 1):338-9. PubMed ID: 2116511
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  • 59. A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.
    Morrow G, Revsin B, Clark R, Lebowitz J, Whelan DT.
    Clin Chim Acta; 1978 Apr 03; 85(1):67-72. PubMed ID: 25730
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  • 60. Serial study of the urinary metabolites in newborn children.
    Tănase I, Ciortoloman H, Grigorescu G, Popescu M.
    Physiologie; 1977 Apr 03; 14(2):101-5. PubMed ID: 405681
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