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Journal Abstract Search

276 related items for PubMed ID: 22613102

  • 1. [Clinical analysis of organic acidemia in neonates from neonatal intensive care units].
    Xu FL, Fan T, Duan JJ, Chen D.
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 May; 14(5):336-9. PubMed ID: 22613102
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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
    [Abstract] [Full Text] [Related]

  • 4. [Metabolic disorders of branched-chain amino acids: most common forms of organic aciduria in the neonatal period].
    Sperl W, Lehnert W.
    Klin Padiatr; 1990 Jun; 202(5):334-9. PubMed ID: 2214593
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  • 5. [Diagnosis of inborn errors of metabolism using tandem mass spectrometry and gas chromatography mass spectrometry].
    Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Jin J, Gu XF.
    Zhonghua Yi Xue Za Zhi; 2008 Aug 05; 88(30):2122-6. PubMed ID: 19080473
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  • 7. Branched-chain organic acidurias.
    Ogier de Baulny H, Saudubray JM.
    Semin Neonatol; 2002 Feb 05; 7(1):65-74. PubMed ID: 12069539
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  • 8. An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand.
    Thiboonboon K, Leelahavarong P, Wattanasirichaigoon D, Vatanavicharn N, Wasant P, Shotelersuk V, Pangkanon S, Kuptanon C, Chaisomchit S, Teerawattananon Y.
    PLoS One; 2015 Feb 05; 10(8):e0134782. PubMed ID: 26258410
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  • 9. Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
    Bower A, Imbard A, Benoist JF, Pichard S, Rigal O, Baud O, Schiff M.
    Sci Rep; 2019 Oct 01; 9(1):14098. PubMed ID: 31575911
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  • 11. Clinical characteristics of neonates with inborn errors of metabolism detected by Tandem MS analysis in Oman.
    Joshi SN, Venugopalan P.
    Brain Dev; 2007 Oct 01; 29(9):543-6. PubMed ID: 17314022
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  • 12. Maple syrup urine disease in Thai infants.
    Pangkanon S, Charoensiriwatana W, Sangtawesin V.
    J Med Assoc Thai; 2008 Oct 01; 91 Suppl 3():S41-4. PubMed ID: 19255991
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  • 16. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease].
    Raven EJ.
    Ned Tijdschr Geneeskd; 1969 Oct 18; 113(42):1850-3. PubMed ID: 5344645
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  • 17. [Disease spectrum analysis of children with inherited metabolic diseases detected by gas chromatography-mass spectrometry of urinary organic acids].
    Bu XX, Qiu WJ, Zhang HW, Gao XL, Zhan X, Chen T, Xu F, Liu YC, Gu XF, Han LS.
    Zhonghua Er Ke Za Zhi; 2022 Jun 02; 60(6):522-526. PubMed ID: 35658356
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  • 18. Pancreatitis in patients with organic acidemias.
    Kahler SG, Sherwood WG, Woolf D, Lawless ST, Zaritsky A, Bonham J, Taylor CJ, Clarke JT, Durie P, Leonard JV.
    J Pediatr; 1994 Feb 02; 124(2):239-43. PubMed ID: 8301430
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  • 19. Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosis.
    Ma X, Zhang Y, Yang Y, Liu X, Yang Z, Bao X, Qin J, Wu X.
    Brain Dev; 2011 Oct 02; 33(9):790-5. PubMed ID: 21764232
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