BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 531662)

  • 1. [Genetic screening of newborns].
    Vulović D; Vilhar N; Banićević M; Sićević S; Hajduković R
    Srp Arh Celok Lek; 1979 Mar; 107(3):269-81. PubMed ID: 531662
    [No Abstract]   [Full Text] [Related]  

  • 2. Neonatal screening for biochemical disorders.
    Holton JB
    Br J Hosp Med; 1988 Apr; 39(4):317-9, 322-4. PubMed ID: 3164641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [After PKU and hypothyroidism, what other screening?].
    Frézal J; Briard ML; Saudubray JM
    J Genet Hum; 1981 Mar; 29(1):47-57. PubMed ID: 7334341
    [No Abstract]   [Full Text] [Related]  

  • 4. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C
    Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974
    [No Abstract]   [Full Text] [Related]  

  • 5. Neonatal screening for inborn errors of metabolism: update.
    Seashore MR
    Semin Perinatol; 1990 Dec; 14(6):431-8. PubMed ID: 2077663
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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; 10():69-85. PubMed ID: 7349406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Early diagnosis of congenital metabolic diseases].
    Böhles H; Stehr K
    Fortschr Med; 1980 Jul; 98(25):955-7. PubMed ID: 7450633
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening for genetic disorders.
    Berry HK
    Fed Proc; 1975 Nov; 34(12):2134-9. PubMed ID: 1102335
    [No Abstract]   [Full Text] [Related]  

  • 9. Early detection of inborn errors of metabolism in Poland.
    Bozkowa K; Cabalska B; Duczynska N; Grodzka Z; Lenartowska I; Helwich E
    Acta Anthropogenet; 1983; 7(4):373-81. PubMed ID: 6680316
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Newborn screening.
    Sahai I; Marsden D
    Crit Rev Clin Lab Sci; 2009; 46(2):55-82. PubMed ID: 19255915
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progress in screening for inborn errors of metabolism.
    Watts RW
    Experientia; 1978 Feb; 34(2):143-52. PubMed ID: 624338
    [No Abstract]   [Full Text] [Related]  

  • 12. Newborn screening: the role of the obstetrician.
    Larsson A; Therrell BL
    Clin Obstet Gynecol; 2002 Sep; 45(3):697-710; discussion 730-2. PubMed ID: 12370609
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic screening of the newborn in Australia. Results for 1978.
    Pitt D; Connelly J; Francis I; Wilcken B; Brown DA; Hill G; Masters P; Tucker RG; Raby J; McFarlane J
    Med J Aust; 1979 Sep; 2(5):272-3. PubMed ID: 514173
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Newborn screening for metabolic disorders.
    Mamunes P
    Clin Perinatol; 1976 Mar; 3(1):231-50. PubMed ID: 821691
    [No Abstract]   [Full Text] [Related]  

  • 15. Diagnosis of inborn errors of metabolism.
    Wong HB
    J Singapore Paediatr Soc; 1986; 28(1-2):45-53. PubMed ID: 3762077
    [No Abstract]   [Full Text] [Related]  

  • 16. [Current problems in the detection of inborn errors of metabolism using screening tests in newborns].
    Hübschmann K
    Padiatr Grenzgeb; 1971; 10(2):115-25. PubMed ID: 5148734
    [No Abstract]   [Full Text] [Related]  

  • 17. State screening for metabolic disorders in newborns.
    Stevens MB; Rigilano JC; Wilson CC
    Am Fam Physician; 1988 Apr; 37(4):223-8. PubMed ID: 3358346
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rationales for genetic screening.
    Gitzelmann R
    Prog Clin Biol Res; 1982; 103 Pt B():425-36. PubMed ID: 7163237
    [No Abstract]   [Full Text] [Related]  

  • 19. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
    World Health Organ Tech Rep Ser; 1968; 401():1-57. PubMed ID: 4973455
    [No Abstract]   [Full Text] [Related]  

  • 20. Public health explores expanding newborn screening for cystic fibrosis, congenital adrenal hyperplasia, and medium-chain acyl coenzyme A dehydrogenase deficiency (MCAD).
    Rhoades E; King P
    J Okla State Med Assoc; 2001 Apr; 94(4):129-32. PubMed ID: 11392180
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.