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Journal Abstract Search

264 related items for PubMed ID: 22481200

  • 1. Aminoacidopathies and organic acidurias in Tunisia: a retrospective survey over 23 years.
    Hadj-Taieb S, Nasrallah F, Hammami MB, Elasmi M, Sanhaji H, Moncef F, Kaabachi N.
    Tunis Med; 2012 Mar; 90(3):258-61. PubMed ID: 22481200
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  • 2. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience.
    Karam PE, Habbal MZ, Mikati MA, Zaatari GE, Cortas NK, Daher RT.
    Clin Biochem; 2013 Dec; 46(18):1787-92. PubMed ID: 23994778
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  • 3. [Abnormal findings during newborn period of 160 patients with early-onset methylmalonic aciduria].
    Liu YP, Ma YY, Wu TF, Wang Q, Li XY, Ding Y, Song JQ, Huang Y, Yang YL.
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):410-4. PubMed ID: 22931934
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  • 5. Branched-chain organic acidurias.
    Ogier de Baulny H, Saudubray JM.
    Semin Neonatol; 2002 Feb; 7(1):65-74. PubMed ID: 12069539
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  • 7. Detection of inborn errors of metabolism using GC-MS: over 3 years of experience in southern China.
    Jiang M, Liu L, Mei H, Li X, Cheng J, Cai Y.
    J Pediatr Endocrinol Metab; 2015 Mar; 28(3-4):375-80. PubMed ID: 25781538
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  • 9. Screening newborns for multiple organic acidurias in dried filter paper urine samples: method development.
    Tuchman M, McCann MT, Johnson PE, Lemieux B.
    Pediatr Res; 1991 Oct; 30(4):315-21. PubMed ID: 1956713
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  • 10. 'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry.
    Dionisi-Vici C, Deodato F, Röschinger W, Rhead W, Wilcken B.
    J Inherit Metab Dis; 2006 Oct; 29(2-3):383-9. PubMed ID: 16763906
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  • 11. Selective screening for organic acidemias by urine organic acid GC-MS analysis in Brazil: fifteen-year experience.
    Wajner M, Coelho Dde M, Ingrassia R, de Oliveira AB, Busanello EN, Raymond K, Flores Pires R, de Souza CF, Giugliani R, Vargas CR.
    Clin Chim Acta; 2009 Feb; 400(1-2):77-81. PubMed ID: 18992233
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  • 12. Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period.
    Divry P, Vianey-Liaud C, Cotte J.
    Biomed Environ Mass Spectrom; 1987 Nov; 14(11):663-8. PubMed ID: 2962675
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  • 15. [Metabolic disorders of branched-chain amino acids: most common forms of organic aciduria in the neonatal period].
    Sperl W, Lehnert W.
    Klin Padiatr; 1990 Nov; 202(5):334-9. PubMed ID: 2214593
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  • 18. Selective screening for inborn errors of metabolism and secondary methylmalonic aciduria in pregnancy at high risk district of neural tube defects: a human metabolome study by GC-MS in China.
    Song YZ, Li BX, Hao H, Xin RL, Zhang T, Zhang CH, Kobayashi K, Wang ZN, Zheng XY.
    Clin Biochem; 2008 May; 41(7-8):616-20. PubMed ID: 18291102
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  • 19. Organic acidurias in Egyptian children: The urge for high-risk screening.
    Mehaney DA, Seliem ZS, Selim LA, Khalil MS, Abou-Youssef HS, Elsayed EM, Abdou DM, Rizzo C, Dioniasi-Vici C, Abdelazim AM, Elkady SH.
    Pediatr Int; 2023 Jan; 65(1):e15469. PubMed ID: 36609685
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  • 20. "Classical organic acidurias": diagnosis and pathogenesis.
    Villani GR, Gallo G, Scolamiero E, Salvatore F, Ruoppolo M.
    Clin Exp Med; 2017 Aug; 17(3):305-323. PubMed ID: 27613073
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