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PUBMED FOR HANDHELDS

Journal Abstract Search


168 related items for PubMed ID: 691356

  • 1. [Methylmalonic aciduria].
    Onishi S.
    Nihon Rinsho; 1978 May; Suppl():1362-3. PubMed ID: 691356
    [No Abstract] [Full Text] [Related]

  • 2. Methylmalonic aciduria (1 case report).
    Yuan LF, Zhao SM, Luo HY, Huang XH, Guo YZ, Xu JZ, Xu YY.
    Proc Chin Acad Med Sci Peking Union Med Coll; 1987 May; 2(3):183-5. PubMed ID: 3444838
    [No Abstract] [Full Text] [Related]

  • 3. [Methylmalonic aciduria - diagnosis and therapy using as example 2 cases of this genetic metabolic disorder].
    Lubs H, Seidlitz G, Pfau E.
    Padiatr Grenzgeb; 1982 May; 21(4):319-26. PubMed ID: 7177670
    [No Abstract] [Full Text] [Related]

  • 4. [Pharmacologic and dietetic treatment of 2 siblings with atypical methylmalonic aciduria].
    Duillo MT, Poggi L, Cortese M, de Toni T, Di Rocco M.
    Minerva Pediatr; 1984 Oct 31; 36(20):999-1002. PubMed ID: 6531009
    [No Abstract] [Full Text] [Related]

  • 5. Corneal involvement in methylmalonic aciduria.
    Haney ML, Jeffrey CP, Cavanagh HD.
    Ann Ophthalmol; 1981 Jan 31; 13(1):81-3. PubMed ID: 7247163
    [No Abstract] [Full Text] [Related]

  • 6. [Carnitine in the treatment of methylmalonic aciduria (MMA)].
    Penn D, Schmidt H, Otten A, Schmidt-Sommerfeld E.
    Monatsschr Kinderheilkd; 1986 Oct 31; 134(10):758-61. PubMed ID: 2879226
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  • 13. B12-unresponsive methylmalonic aciduria in a female infant.
    Vecchio F, Carnevale F, Paganetti G, di Bitonto G, Penza R, Francioso G.
    J Inherit Metab Dis; 1980 Oct 31; 3(3):91-2. PubMed ID: 6775146
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  • 14. Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduria.
    Linnell JC, Matthews DM, Mudd SH, Uhlendorf BW, Wise IJ.
    Pediatr Res; 1976 Mar 31; 10(3):179-83. PubMed ID: 2896
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  • 16. Methylmalonic aciduria in a black female child with congenital short femur on the right side.
    Meiring JL, Strydom AJ.
    J Inherit Metab Dis; 1981 Mar 31; 4(2):107-8. PubMed ID: 6790839
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  • 18. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy.
    Shinnar S, Singer HS.
    N Engl J Med; 1984 Aug 16; 311(7):451-4. PubMed ID: 6749192
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  • 20. [A case of metabolic encephalopathy caused by vitamin B 12-dependent methylmalonicoaciduria].
    Capece G, Giliberti P, Militerni R, Pignero A.
    Acta Neurol (Napoli); 1981 Feb 16; 3(1):254-9. PubMed ID: 6965256
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