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3. [Suspected clinical diagnosis of genetic metabolic disorders in prevention and daily practice]. Grosser V; Knapp A Z Arztl Fortbild (Jena); 1973 Dec; 67(24):1233-8. PubMed ID: 4791811 [No Abstract] [Full Text] [Related]
4. Screening for inborn errors of metabolism. Report of a WHO Scientific Group. World Health Organ Tech Rep Ser; 1968; 401():1-57. PubMed ID: 4973455 [No Abstract] [Full Text] [Related]
5. Inborn errors of metabolism: the essentials of clinical diagnosis. Roth KS Clin Pediatr (Phila); 1991 Mar; 30(3):183-90. PubMed ID: 2009725 [No Abstract] [Full Text] [Related]
6. Inherited metabolic disease and the eye. Eichhorn MM Sight Sav Rev; 1971; 41(2):55-64. PubMed ID: 4937807 [No Abstract] [Full Text] [Related]
11. [Hereditary amino acid metabolism disorders. Indications for early diagnosis]. Kroll S; Zebisch P; Toussaint W Fortschr Med; 1972 Apr; 90(11):423-8. PubMed ID: 4680607 [No Abstract] [Full Text] [Related]
12. Study of hereditary metabolic diseases using in vitro techniques. Hsia DY Metabolism; 1970 Apr; 19(4):309-39. PubMed ID: 4190983 [No Abstract] [Full Text] [Related]
13. [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 [TBL] [Abstract][Full Text] [Related]
14. Laboratory approaches for inherited neurometabolic diseases. Kolodny EH; Yatziv S Dev Med Child Neurol; 1985 Apr; 27(2):252-7. PubMed ID: 3996782 [No Abstract] [Full Text] [Related]
15. Ocular manifestations in aminoacidopathies. François J Monogr Hum Genet; 1972; 6():99-113. PubMed ID: 4541412 [No Abstract] [Full Text] [Related]
16. [Ocular manifestations of homocystinuria, report of two cases]. Mukuno K; Matsui K; Haraguchi H Nippon Ganka Gakkai Zasshi; 1967 Jan; 71(1):66-73. PubMed ID: 6068744 [No Abstract] [Full Text] [Related]
17. [Detection of metabolic diseases]. Adriaenssens K; Van Sande M Acta Neurol Psychiatr Belg; 1968 Oct; 68(10):719-28. PubMed ID: 4976725 [No Abstract] [Full Text] [Related]
18. [Biochemical diagnosis of rare hereditary metabolic disorders. Experiences from a patient sample of the Innsbruck University Pediatric Clinic 1984-1987]. Sperl W Padiatr Padol; 1990; 25(3):157-67. PubMed ID: 2381732 [TBL] [Abstract][Full Text] [Related]