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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

328 related articles for article (PubMed ID: 5709563)

  • 41. Phenylketonuria. Some current problems.
    Komrower GM
    Arch Dis Child; 1970 Feb; 45(239):2-4. PubMed ID: 5440203
    [No Abstract]   [Full Text] [Related]  

  • 42. The current status of newborn screening.
    Levy HL; Mitchell ML
    Hosp Pract (Off Ed); 1982 Jul; 17(7):89-97. PubMed ID: 6809575
    [No Abstract]   [Full Text] [Related]  

  • 43. Cuban neonatal screening of phenylketonuria using an ultramicro-fluorometric test.
    González EC; Frómeta A; del Río L; Castells E; Robaina MS; García SM; Licourt T; Arteaga AL; Martínez L
    Clin Chim Acta; 2009 Apr; 402(1-2):129-32. PubMed ID: 19168043
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Did the change of technique of screening investigations influence on improvement of test credibility in recognizing and differentiating diagnostics of hiperphenylalaninemias?].
    Didycz B; Lemańska D; Słuszniak A
    Przegl Lek; 2009; 66(1-2):11-3. PubMed ID: 19485249
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prospective study of early neonatal screening for phenylketonuria.
    Meryash DL; Levy HL; Guthrie R; Warner R; Bloom S; Carr JR
    N Engl J Med; 1981 Jan; 304(5):294-6. PubMed ID: 7442762
    [No Abstract]   [Full Text] [Related]  

  • 46. On indications for treatment of the hyperphenylalaninemic neonate.
    Güttler F; Wamberg E
    Acta Paediatr Scand; 1977 May; 66(3):339-44. PubMed ID: 868515
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages].
    Simková M; Hyánek J; Karger P; Hoza J; Holub J; Viletová H
    Cesk Pediatr; 1976 Nov; 31(11):619-21. PubMed ID: 1035139
    [No Abstract]   [Full Text] [Related]  

  • 48. [Phenylketonuria, its detection and control with thin layer chromatography].
    Huth E; Klingmüller V
    Monatsschr Kinderheilkd (1902); 1968 Jun; 116(6):294-6. PubMed ID: 5718288
    [No Abstract]   [Full Text] [Related]  

  • 49. Screening program for early detection of phenylketonuria in the newborn in Israel.
    Cohen BE; Szeinberg A; Peled I; Szeinberg B; Bar-Or R
    Isr J Med Sci; 1966; 2(2):156-64. PubMed ID: 5912550
    [No Abstract]   [Full Text] [Related]  

  • 50. [The early diagnosis of phenylketonuria].
    Bernat K
    Pieleg Polozna; 1989; (6):4, 23. PubMed ID: 2608742
    [No Abstract]   [Full Text] [Related]  

  • 51. Detection of phenylketonuria in the very early newborn blood specimen.
    Doherty LB; Rohr FJ; Levy HL
    Pediatrics; 1991 Feb; 87(2):240-4. PubMed ID: 1987536
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Neonatal screening for phenylketonuria. Comparison of 3 methods for mass screening].
    Poncini L; Caramello S; Poncini D
    Minerva Pediatr; 1979 Sep; 31(18):1309-14. PubMed ID: 545128
    [No Abstract]   [Full Text] [Related]  

  • 53. Elevated phenylalanine on newborn screening: follow-up testing may reveal undiagnosed galactosaemia.
    Shakespeare L; Downing M; Allen J; Casbolt AM; Ellin S; Maloney M; Race G; Bonham J
    Ann Clin Biochem; 2010 Nov; 47(Pt 6):567-9. PubMed ID: 20947531
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Ion-exchange thin-layer chromatographic screening test for phenylketonuria and other aminoacidaemias.
    Kovács J
    Acta Paediatr Acad Sci Hung; 1973; 14(3):165-9. PubMed ID: 4785695
    [No Abstract]   [Full Text] [Related]  

  • 55. An evaluation of routine follow-up blood screening of infants for phenylketonuria.
    Sepe SJ; Levy HL; Mount FW
    N Engl J Med; 1979 Mar; 300(11):606-9. PubMed ID: 33334
    [No Abstract]   [Full Text] [Related]  

  • 56. Population screening by Guthrie test for phenylketonuria in South-east Scotland. Report by the consultant paediatricians and medical officers of health of the S.E. Scotland Hospital Region.
    Br Med J; 1968 Mar; 1(5593):674-6. PubMed ID: 5640647
    [No Abstract]   [Full Text] [Related]  

  • 57. [Mass testing of infants for prevention of phenylpyruvic oligophrenia (phenylketonuria)].
    Menne F
    Hippokrates; 1966 Aug; 37(15):601-5. PubMed ID: 5927426
    [No Abstract]   [Full Text] [Related]  

  • 58. Neonatal screening for phenylketonuria.
    Pediatrics; 1984 May; 73(5):737-40. PubMed ID: 6718135
    [No Abstract]   [Full Text] [Related]  

  • 59. Austria newborn screening programme for inborn errors of metabolism.
    Thalhammer O
    Acta Univ Carol Med Monogr; 1973; 56():79-82. PubMed ID: 4791784
    [No Abstract]   [Full Text] [Related]  

  • 60. Newborn screening for phenylketonuria: predictive validity as a function of age.
    McCabe ER; McCabe L; Mosher GA; Allen RJ; Berman JL
    Pediatrics; 1983 Sep; 72(3):390-8. PubMed ID: 6889045
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.