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72. [Autoanalysis in the biochemical study of metabolic and hereditary diseases]. Lemonnier A; Charpentier C Ann Biol Clin (Paris); 1973; 31(6):509-24. PubMed ID: 4594986 [No Abstract] [Full Text] [Related]
74. [Hereditary metabolic diseases in adults]. Saudubray JM; Nuoffer JM; de Lonlay P; Castelnau P; Touati G Rev Med Interne; 1998; 19 Suppl 3():366S-375S. PubMed ID: 9885858 [No Abstract] [Full Text] [Related]
75. [Screening of congenital metabolic anomalies. High risk screening]. Isshiki G Nihon Rinsho; 1979 Jun; Suppl():1610-5. PubMed ID: 490953 [No Abstract] [Full Text] [Related]
76. Inborn errors of metabolism as a cause of neurological disease in adults: an approach to investigation. Gray RG; Preece MA; Green SH; Whitehouse W; Winer J; Green A J Neurol Neurosurg Psychiatry; 2000 Jul; 69(1):5-12. PubMed ID: 10864596 [No Abstract] [Full Text] [Related]
77. Inborn errors of metabolism: screening for heterozygotes using hair roots. de Bruyn CH; Vermorken AJ; Oei TL; Geerts SJ Br J Dermatol; 1979 Jul; 101(1):111-4. PubMed ID: 475981 [No Abstract] [Full Text] [Related]
78. Autism and inborn errors of metabolism: how much is enough? Asato MR; Goldstein AC; Schiff M Dev Med Child Neurol; 2015 Sep; 57(9):788-9. PubMed ID: 25873003 [No Abstract] [Full Text] [Related]
80. The diagnosis of inborn errors of metabolism by examination of the genotype. Hill RE Clin Chim Acta; 1993 Jul; 217(1):3-14. PubMed ID: 8222281 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]