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.
70 related articles for article (PubMed ID: 698997)
21. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism. Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719 [TBL] [Abstract][Full Text] [Related]
23. [Screening method for the detection of urine with inherited basic amino acidopathies by thin-layer chromatography (author's transl)]. Fukaya J; Iwase M; Kanno T Rinsho Byori; 1978 Nov; 26(11):979-82. PubMed ID: 731965 [No Abstract] [Full Text] [Related]
24. [Phenylketonuria and hyperphenylalaninemia: clinico-genetic classification of 14 forms]. Annenkov GA Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):351-6. PubMed ID: 6720175 [TBL] [Abstract][Full Text] [Related]
25. [Frequency and prevention of genetic defects and diseases (author's transl)]. Witkowski R; Grossmann P Arztl Jugendkd; 1980 Feb; 71(1):21-6. PubMed ID: 7395643 [No Abstract] [Full Text] [Related]
26. [Screening for aminoacidopathies in newborns by means of an aminoacid analyzer. Reference values and statistical determinations (author's transl)]. Antonozzi I; Del Castello PG; Morisi G; Ceccarelli P Ann Ist Super Sanita; 1978; 14(4):781-91. PubMed ID: 756692 [TBL] [Abstract][Full Text] [Related]
27. Dietary treatment of destructive behavior associated with hyperphenylalaninemia. Baumeister AA; Baumeister AA Clin Neuropharmacol; 1998; 21(1):18-27. PubMed ID: 9579281 [TBL] [Abstract][Full Text] [Related]
28. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism]. Charpentier C; Lemonnier A Ann Biol Clin (Paris); 1969; 27(5):297-323. PubMed ID: 4897889 [No Abstract] [Full Text] [Related]
36. The philosophy and practice of screening for inherited diseases. Komrower GM Pediatrics; 1974 Feb; 53(2):182-8. PubMed ID: 4272866 [No Abstract] [Full Text] [Related]
38. Anomalous phenylalanine loading responses in relation to cleft lip and cleft palate. Tocci PM; Beber B Pediatrics; 1973 Jul; 52(1):109-13. PubMed ID: 4737485 [No Abstract] [Full Text] [Related]
39. [Problems in the detection of hereditary diseases studied in the light of frequent examples]. Vis HL Brux Med; 1972 Feb; 52(2):95-100. PubMed ID: 4551157 [No Abstract] [Full Text] [Related]
40. [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] [Previous] [Next] [New Search]