These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. [Simultaneous thin-layer chromatography of blood and urine samples for the diagnosis of hereditary amino acid metabolism disorders]. Peters WH; Lubs H; Knapp A Z Arztl Fortbild (Jena); 1974 Jul; 68(14):716-25. PubMed ID: 4216183 [No Abstract] [Full Text] [Related]
5. [The early recognition of congenital metabolic diseases]. Steuber W Munch Med Wochenschr; 1971 Mar; 113(13):463-7. PubMed ID: 5108281 [No Abstract] [Full Text] [Related]
6. Some inborn errors of metabolism. Barbor P Nurs Mirror; 1978 Jul; 147(3):21-2. PubMed ID: 248774 [No Abstract] [Full Text] [Related]
7. 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]
9. [Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests]. Schmid-Rüter E Fortschr Med; 1978 Jun; 96(24):1289-93. PubMed ID: 96002 [TBL] [Abstract][Full Text] [Related]
10. The value of screening in paediatrics. Carter RA J R Coll Physicians Lond; 1976 Jan; 10(2):153-60. PubMed ID: 54421 [No Abstract] [Full Text] [Related]
11. Screening for inborn errors of metabolism in infancy. Hudson FP Nurs Mirror Midwives J; 1975 Aug; 141(9):64-6. PubMed ID: 1041391 [No Abstract] [Full Text] [Related]
12. Screening for metabolic disorders. How are we doing? Irons M Pediatr Clin North Am; 1993 Oct; 40(5):1073-85. PubMed ID: 8414711 [TBL] [Abstract][Full Text] [Related]
13. [Test program for the earlydetection of inborn errors of metabolism]. Thlhamer O Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):37-8. PubMed ID: 5398916 [No Abstract] [Full Text] [Related]
14. [Dietetics in hereditary enzyme deficiencies]. Royer P Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674 [No Abstract] [Full Text] [Related]
15. Newborn screening: the role of the obstetrician. Larsson A; Therrell BL Clin Obstet Gynecol; 2002 Sep; 45(3):697-710; discussion 730-2. PubMed ID: 12370609 [No Abstract] [Full Text] [Related]
16. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl]. Menne F; Otte HJ; Krüger M; Winterhoff D MMW Munch Med Wochenschr; 1978 May; 120(18):619-22. PubMed ID: 306535 [TBL] [Abstract][Full Text] [Related]
17. 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 [No Abstract] [Full Text] [Related]
18. [A screening test for phenylketonuria using a paper chromatography method]. Halvorsen S; Skjelkvåle L Lakartidningen; 1974 Mar; 71(12):1166-7. PubMed ID: 4821497 [No Abstract] [Full Text] [Related]
19. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods]. Kroll S; Zebisch P; Toussaint W Fortschr Med; 1972 Apr; 90(11):430-1. PubMed ID: 4681731 [No Abstract] [Full Text] [Related]
20. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report]. Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466 [No Abstract] [Full Text] [Related] [Next] [New Search]