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2. [The early recognition of congenital metabolic diseases]. Steuber W. Munch Med Wochenschr; 1971 Mar 26; 113(13):463-7. PubMed ID: 5108281 [No Abstract] [Full Text] [Related]
3. [Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2]. Menne F, Enzenauer J, Matz D. Med Klin; 1976 Apr 30; 71(18):779-85. PubMed ID: 178988 [No Abstract] [Full Text] [Related]
4. Some inborn errors of metabolism. Barbor P. Nurs Mirror; 1978 Jul 20; 147(3):21-2. PubMed ID: 248774 [No Abstract] [Full Text] [Related]
5. [Early diagnosis of mental deficiency caused by metabolic diseases in children]. Bickel H. Landarzt; 1965 May 10; 41(13):548-9. PubMed ID: 5827014 [No Abstract] [Full Text] [Related]
6. [Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests]. Schmid-Rüter E. Fortschr Med; 1978 Jun 22; 96(24):1289-93. PubMed ID: 96002 [Abstract] [Full Text] [Related]
7. [Current views on therapy of some dysmetabolic oligophrenias]. Giovannini M. Minerva Pediatr; 1967 Dec 22; 19(51):2286-90. PubMed ID: 5607848 [No Abstract] [Full Text] [Related]
8. [Screening and therapy of 6 metabolic diseases of hereditary nature which are possible causes of mental retardation: screening of 1,900,000 newborn infants since the year 1965]. Menne F. Clin Ter; 1979 Mar 15; 88(5):445-59. PubMed ID: 466967 [No Abstract] [Full Text] [Related]
9. Screening for inborn errors of metabolism in infancy. Hudson FP. Nurs Mirror Midwives J; 1975 Aug 28; 141(9):64-6. PubMed ID: 1041391 [No Abstract] [Full Text] [Related]
10. Screening for inborn errors of metabolism. Report of a WHO Scientific Group. World Health Organ Tech Rep Ser; 1968 Aug 28; 401():1-57. PubMed ID: 4973455 [No Abstract] [Full Text] [Related]
11. [Test program for the earlydetection of inborn errors of metabolism]. Thlhamer O. Monatsschr Kinderheilkd (1902); 1969 Jan 28; 117(1):37-8. PubMed ID: 5398916 [No Abstract] [Full Text] [Related]
12. Neonatal screening tests. Mamunes P. Pediatr Clin North Am; 1980 Nov 28; 27(4):733-51. PubMed ID: 7005846 [No Abstract] [Full Text] [Related]
13. [Combined forms of metabolic errors detected in newborn infants]. Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V. Physiologie; 1978 Nov 28; 15(4):239-43. PubMed ID: 106407 [No Abstract] [Full Text] [Related]
14. [Screening of the Westphalia-Lippe newborns of 1977 for phenylketonuria, histidinemia, homocystinuria and maple syrup disease. Furthermore a pilot study of galactosemia and galactokinase deficiency disease]. Menne F, Otte HJ, Krüger M, Winterhoff D. MMW Munch Med Wochenschr; 1979 Jun 22; 121(25):833-4. PubMed ID: 111089 [No Abstract] [Full Text] [Related]
15. Screening for metabolic disorders. How are we doing? Irons M. Pediatr Clin North Am; 1993 Oct 22; 40(5):1073-85. PubMed ID: 8414711 [Abstract] [Full Text] [Related]
16. Laboratory approaches for inherited neurometabolic diseases. Kolodny EH, Yatziv S. Dev Med Child Neurol; 1985 Apr 22; 27(2):252-7. PubMed ID: 3996782 [No Abstract] [Full Text] [Related]
17. Newborn screening: the role of the obstetrician. Larsson A, Therrell BL. Clin Obstet Gynecol; 2002 Sep 22; 45(3):697-710; discussion 730-2. PubMed ID: 12370609 [No Abstract] [Full Text] [Related]
18. [Diagnosis of inborn errors of metabolism. (principles and results of investigation of 3,000 persons)]. Farriaux JP, Adam E, Fontaine G, Delecour M. Lille Med; 1968 Oct 22; 13(8):864-72. PubMed ID: 5743598 [No Abstract] [Full Text] [Related]
19. [Screening for congenital metabolic disorders. Indication and results]. Bickel H. Monatsschr Kinderheilkd; 1983 Jun 22; 131(6):323-7. PubMed ID: 6888386 [No Abstract] [Full Text] [Related]
20. [Dietetics in hereditary enzyme deficiencies]. Royer P. Sem Hop; 1970 Feb 26; 46(10):653-9. PubMed ID: 4314674 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]