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3. [Diagnostic methods for the detection of amino acid metabolism disorders]. Lutz P Monatsschr Kinderheilkd (1902); 1973 May; 121(5):184-9. PubMed ID: 4197345 [No Abstract] [Full Text] [Related]
4. [Chromatographic analysis in the diagnosis of metabolic aminoacidopathies]. Sietti C Minerva Pediatr; 1971 Dec; 23(51):2125-8. PubMed ID: 5136312 [No Abstract] [Full Text] [Related]
5. [Personal experience with chromatographic methods of demonstrating aminated substances (amino acids and amines)]. Berio A Minerva Pediatr; 1968 Mar; 20(10):536-45. PubMed ID: 5739013 [No Abstract] [Full Text] [Related]
6. [Hyperaminoacidemia and hyperaminoaciduria of benign nature and their diagnostic values]. Hyánek J; Homolka J; Tauchmanová H; Soukupová Z; Kunová V Cesk Pediatr; 1977 Feb; 32(2):85-9. PubMed ID: 862120 [No Abstract] [Full Text] [Related]
7. [Our preliminary experiences with a unidimensional paper-chromatographic technic for the study of aminoacidopathies and pathological infantile aminoacidurias]. Scorza PA; Berni M; Cicognani A Clin Pediatr (Bologna); 1967 May; 49(5):246-56. PubMed ID: 6083020 [No Abstract] [Full Text] [Related]
8. A sensitive chromatographic technique for screening of amino acid metabolic defects in the newborn. Lato M; Rufini S; Ghebregzabher M; Ciuffini G; Mezzetti T Clin Chim Acta; 1974 Jun; 53(3):273-80. PubMed ID: 4858769 [No Abstract] [Full Text] [Related]
9. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms]. Boisse J Presse Med (1893); 1968 Apr; 76(19):903-6. PubMed ID: 5645352 [No Abstract] [Full Text] [Related]
10. [Organized detection of hereditary metabolic diseases. Amino acidopathies and organic acidurias]. Kaabachi N; Mebazaa A; Hamza L; Ben Miled S; Abdelmoula J Tunis Med; 1989 Nov; 67(11):697-701. PubMed ID: 2595818 [No Abstract] [Full Text] [Related]
11. Selective newborn screening of inborn errors of amino acids, organic acids and fatty acids metabolism in the Kingdom of Bahrain. Golbahar J; Al-Jishi EA; Altayab DD; Carreon E; Bakhiet M; Alkhayyat H Mol Genet Metab; 2013; 110(1-2):98-101. PubMed ID: 23916421 [TBL] [Abstract][Full Text] [Related]
12. [Screening on aminoacid opathies in newborn infants]. Stoppoloni G; Santinelli R Pediatria (Napoli); 1976 Dec; 84(4):604-16. PubMed ID: 1035798 [No Abstract] [Full Text] [Related]
13. Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males. Campbell AG; Rosenberg LE; Snodgrass PJ; Nuzum CT N Engl J Med; 1973 Jan; 288(1):1-6. PubMed ID: 4681895 [No Abstract] [Full Text] [Related]
15. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles]. Plöchl E Wien Med Wochenschr; 1970 Oct; 120(41):707-11. PubMed ID: 4918107 [No Abstract] [Full Text] [Related]
16. [Amino-aciduria and amino-acidemia as a clinical and diagnostic problem in child neuropsychiatry]. Milovanović D; Radojcić B Srp Arh Celok Lek; 1976 Jun; 104(6):457-62. PubMed ID: 1025761 [No Abstract] [Full Text] [Related]