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 *

122 related articles for article (PubMed ID: 1103077)

  • 41. Laboratory aspects of phenylketonuria detection and treatment.
    Cahalane SF
    J Clin Pathol; 1969 Jul; 22(4):509. PubMed ID: 5798649
    [No Abstract]   [Full Text] [Related]  

  • 42. [Screening of 80,000 newborn infants at delivery, for amino acid metabolism].
    Greven-Brauns G; Mulkens E
    Arch Belg Med Soc; 1975 Apr; 33(4):253-7. PubMed ID: 1231644
    [No Abstract]   [Full Text] [Related]  

  • 43. [Newborn infant screening program in Switzerland].
    Gitzelmann R
    Bull Schweiz Akad Med Wiss; 1972 Sep; 28(5):294-301. PubMed ID: 4645587
    [No Abstract]   [Full Text] [Related]  

  • 44. 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]  

  • 45. Neonatal blood quality control program.
    Glick MR; Nordschow CD; Oei TO
    Clin Chem; 1978 Aug; 24(8):1423. PubMed ID: 679468
    [No Abstract]   [Full Text] [Related]  

  • 46. 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]  

  • 47. The Guthrie screening test for phenylketonuria: a report on two years participation in the national programme.
    Becroft DM; Horn CR
    N Z Med J; 1969 Apr; 69(443):212-5. PubMed ID: 5254295
    [No Abstract]   [Full Text] [Related]  

  • 48. [Early diagnosis of congenital disorders].
    Méhes K
    Orv Hetil; 1978 Jul; 119(30):1819-23. PubMed ID: 353640
    [No Abstract]   [Full Text] [Related]  

  • 49. Neonatal screening in France.
    Pollitt RJ
    J Inherit Metab Dis; 1983; 6(2):49-50. PubMed ID: 6410117
    [No Abstract]   [Full Text] [Related]  

  • 50. An overview of newborn screening.
    Levy PA
    J Dev Behav Pediatr; 2010 Sep; 31(7):622-31. PubMed ID: 20814260
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The Oregon program of screening for inborn errors of metabolism.
    Ashley CG
    Northwest Med; 1971 Apr; 70(4):268-9. PubMed ID: 5550115
    [No Abstract]   [Full Text] [Related]  

  • 52. Phenylketonuria.
    Br Med J; 1970 Jun; 2(5709):553. PubMed ID: 5526605
    [No Abstract]   [Full Text] [Related]  

  • 53. 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]  

  • 54. [Methods and results of screening newborn infants for aminoacidopathies].
    Bickel H
    Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):650-3. PubMed ID: 979984
    [No Abstract]   [Full Text] [Related]  

  • 55. Results of routine screening for phenylketonuria in early infancy, Northern Ireland (1960-67).
    Carson NA; Carré IJ; Neill DW
    Arch Dis Child; 1968 Apr; 43(228):145-6. PubMed ID: 5645687
    [No Abstract]   [Full Text] [Related]  

  • 56. Phenylketonuria.
    Hudson FP
    Proc R Soc Med; 1967 Nov; 60(11 Part 1):1152-5. PubMed ID: 6060715
    [No Abstract]   [Full Text] [Related]  

  • 57. [Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1].
    Menne F; Enzenauer J; Matz D
    Med Klin; 1976 Apr; 71(17):724-8. PubMed ID: 775276
    [No Abstract]   [Full Text] [Related]  

  • 58. 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]  

  • 59. Prenatal diagnosis of genetic disease.
    Friedmann T
    Sci Am; 1971 Nov; 225(5):34-42. PubMed ID: 5106886
    [No Abstract]   [Full Text] [Related]  

  • 60. Legal and social issues in medical genetics.
    Turner JH; Hayashi TT; Pogoloff DD
    Am J Obstet Gynecol; 1979 May; 134(1):83-99. PubMed ID: 375738
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.