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Journal Abstract Search

255 related items for PubMed ID: 856539

  • 1. An approach to the diagnosis of overwhelming metabolic disease in early infancy.
    Nyhan WL.
    Curr Probl Pediatr; 1977 Apr; ():1-20. PubMed ID: 856539
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  • 3. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V.
    Physiologie; 1978 Apr; 15(4):239-43. PubMed ID: 106407
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  • 6. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia.
    Yahya NA, Ismail Z, Embong KH, Mohamad SA.
    Southeast Asian J Trop Med Public Health; 1995 Apr; 26 Suppl 1():130-3. PubMed ID: 8629091
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  • 8. [Combined use of tandem mass spectrometry with urine gas chromatography/mass spectrometry is useful for diagnosis of inborn errors of metabolism in children].
    Xie LJ, Zhu JX, Zhu XD, Li HJ, Han LS, Gu XF.
    Zhongguo Dang Dai Er Ke Za Zhi; 2008 Feb; 10(1):31-4. PubMed ID: 18289467
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  • 11. Diagnosis and treatment: some diseases, syndromes, and conditions associated with an unusual odor.
    Cone TE.
    Pediatrics; 1968 May; 41(5):993-5. PubMed ID: 5654847
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  • 14. [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)].
    Koepp P, Grüttner R.
    Klin Padiatr; 1975 Jan; 187(1):14-9. PubMed ID: 1168276
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  • 17. 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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  • 19. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968 Mar; 401():1-57. PubMed ID: 4973455
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  • 20. A sensitive chromatographic technique for screening of amino acid metabolic defects in the newborn.
    Lato M, Rufini S, Ghebregzabher M, Ciuffini G, Mezzetti T.
    Clin Chim Acta; 1974 Jun 28; 53(3):273-80. PubMed ID: 4858769
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