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2. [Amino acid composition in blood and urine from healthy newborn infants: screening test for the detection of enxymopathies]. Adrienne S. Orv Hetil; 1969 Jun 08; 110(23):1315-20. PubMed ID: 5794637 [No Abstract] [Full Text] [Related]
3. [Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)]. Lubs H, Baumann H, Kluge G, Machill G. Laryngol Rhinol Otol (Stuttg); 1974 Sep 08; 53(9):648-51. PubMed ID: 4419508 [No Abstract] [Full Text] [Related]
4. [Studies of inborn errors of amino acid metabolism and urinary excretion of -phenylethylamine, using screening methods]. Berio A. Minerva Pediatr; 1972 Jun 23; 24(32):937-41. PubMed ID: 5050421 [No Abstract] [Full Text] [Related]
5. [Results of screening for inborn errors of aminoacid metabolism in adult and infant patients from psychiatric institutions (author's transl)]. Hyánek J, Turek S, Kríz J, Trísková J, Homolka J, Kopejtková H. Cas Lek Cesk; 1975 Mar 14; 114(10-11):307-8. PubMed ID: 1139573 [No Abstract] [Full Text] [Related]
6. [Screening for amino acid diseases: column chromatography of amino acids from a paper sampling]. Castets JC, Jérome H. Arch Fr Pediatr; 1972 Mar 14; 29(6):675-6. PubMed ID: 5078374 [No Abstract] [Full Text] [Related]
7. Quantitative evaluation of thin-layer ion-exchange chromatograms by video-densitometry II. Screening test for amino-acidaemias in blood samples dried on filter paper. Pongor S, Kovács J, Dévényi T. Acta Biochim Biophys Acad Sci Hung; 1978 Mar 14; 13(3):117-21. PubMed ID: 754443 [No Abstract] [Full Text] [Related]
8. [Routine screening for inborn errors using urine filterpaper specimens at age 4-5 weeks (author's transl)]. Schön R, Thalhammer O. Padiatr Padol; 1976 Mar 14; 11(1):319-25. PubMed ID: 1250631 [Abstract] [Full Text] [Related]
9. [Progress in the early detection of inborn errors of metabolism]. Bozkowa K, Cabalska B, Duczyńska N, Grodzka Z, Sendecka E, Nowakowska A, Lenartowska I, Kasperska-Dworak A, Helwich E. Probl Med Wieku Rozwoj; 1981 Mar 14; 10():69-85. PubMed ID: 7349406 [Abstract] [Full Text] [Related]
10. [A system of early screening for inborn errors of metabolism: methods and results for hereditary tyrosinemia]. Bélanger M, Saint-Hilaire B, Bélanger L. Union Med Can; 1973 Feb 14; 102(2):294-302. PubMed ID: 4709460 [No Abstract] [Full Text] [Related]
11. [Thin layer chromatography studies of capillary blood in newborn infants. Evaluation of utility for mass screening]. Coradello H. Klin Padiatr; 1972 Sep 14; 184(5):358-66. PubMed ID: 4673723 [No Abstract] [Full Text] [Related]
12. Chemical diagnosis of amino acid abnormalities. Possibilities and desirabilities. Wadman SK. Acta Univ Carol Med Monogr; 1977 Sep 14; (77 Pt 1):49-69. PubMed ID: 615451 [No Abstract] [Full Text] [Related]
13. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism]. Charpentier C, Lemonnier A. Ann Biol Clin (Paris); 1969 Sep 14; 27(5):297-323. PubMed ID: 4897889 [No Abstract] [Full Text] [Related]
14. [Clinical studies of histidinemia (author's transl)]. Anakura M. Hokkaido Igaku Zasshi; 1981 Jan 14; 56(1):1-15. PubMed ID: 6790399 [Abstract] [Full Text] [Related]
15. Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosis. Hyánek J, Trnka V, Homolka J, Seemanová E, Macek M, Dolezal A, Wünschová N, Hoza J, Kapras J, Kunová V, Tauchmanová H. Acta Univ Carol Med Monogr; 1977 Jan 14; (79 Pt 3):15-21. PubMed ID: 615475 [Abstract] [Full Text] [Related]
16. [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 Jan 14; 14(4):781-91. PubMed ID: 756692 [Abstract] [Full Text] [Related]
17. [Detection of amino acid metabolism inborn errors in neonatal age]. Stoppoloni G. Pediatria (Napoli); 1974 Mar 31; 82(1):79-95. PubMed ID: 4848445 [No Abstract] [Full Text] [Related]
18. [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)]. Koepp P, Grüttner R. Klin Padiatr; 1975 Jan 31; 187(1):14-9. PubMed ID: 1168276 [Abstract] [Full Text] [Related]
19. A review of newborn screening in the era of tandem mass spectrometry: what's new for the pediatric neurologist? Copeland S. Semin Pediatr Neurol; 2008 Sep 31; 15(3):110-6. PubMed ID: 18708000 [Abstract] [Full Text] [Related]
20. [Early detection of inborne errors of metabolism in Switzerland: the problems of hyperphenylanalinemia (author's transl)]. Colombo JP. Ther Umsch; 1974 Aug 31; 31(8):545-52. PubMed ID: 4848540 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]