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 *

125 related articles for article (PubMed ID: 18050122)

  • 1. Assessment of the contribution of insulin-like growth factor I receptor 3174 G-->A polymorphism to the progression of advanced retinopathy of prematurity.
    Shastry BS
    Eur J Ophthalmol; 2007; 17(6):950-3. PubMed ID: 18050122
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lack of association between insulin-like growth factor I receptor G(+3174)A polymorphism and retinopathy of prematurity.
    Balogh A; Derzbach L; Vannay A; Vásárhelyi B
    Graefes Arch Clin Exp Ophthalmol; 2006 Aug; 244(8):1035-8. PubMed ID: 16362313
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lack of association of the VEGF gene promoter (-634 G-->C and -460 C-->T) polymorphism and the risk of advanced retinopathy of prematurity.
    Shastry BS; Qu X
    Graefes Arch Clin Exp Ophthalmol; 2007 May; 245(5):741-3. PubMed ID: 17119993
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A C597-->A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in premature Kuwaiti infants.
    Haider MZ; Devarajan LV; Al-Essa M; Kumar H
    J Biomed Sci; 2002; 9(4):365-70. PubMed ID: 12145535
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphisms of Vascular Endothelial Growth Factor and Retinopathy of Prematurity.
    Ali AA; Hussien NF; Samy RM; Husseiny KA
    J Pediatr Ophthalmol Strabismus; 2015; 52(4):245-53. PubMed ID: 25992764
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Retinopathy of prematurity: mutations in the Norrie disease gene and the risk of progression to advanced stages.
    Haider MZ; Devarajan LV; Al-Essa M; Srivastva BS; Kumar H; Azad R; Rashwan N
    Pediatr Int; 2001 Apr; 43(2):120-3. PubMed ID: 11285060
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity.
    Kwinta P; Bik-Multanowski M; Mitkowska Z; Tomasik T; Pietrzyk JJ
    Graefes Arch Clin Exp Ophthalmol; 2008 Oct; 246(10):1467-75. PubMed ID: 18546007
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Published genetic variants in retinopathy of prematurity: random forest analysis suggests a negligible contribution to risk and severity.
    Dunai G; Vásárhelyi B; Szabó M; Hajdú J; Mészáros G; Tulassay T; Treszl A
    Curr Eye Res; 2008 May; 33(5):501-5. PubMed ID: 18568888
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Postnatal serum insulin-like growth factor I deficiency is associated with retinopathy of prematurity and other complications of premature birth.
    Hellström A; Engström E; Hård AL; Albertsson-Wikland K; Carlsson B; Niklasson A; Löfqvist C; Svensson E; Holm S; Ewald U; Holmström G; Smith LE
    Pediatrics; 2003 Nov; 112(5):1016-20. PubMed ID: 14595040
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Longitudinal postnatal weight and insulin-like growth factor I measurements in the prediction of retinopathy of prematurity.
    Löfqvist C; Andersson E; Sigurdsson J; Engström E; Hård AL; Niklasson A; Smith LE; Hellström A
    Arch Ophthalmol; 2006 Dec; 124(12):1711-8. PubMed ID: 17159030
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity.
    Shastry BS; Pendergast SD; Hartzer MK; Liu X; Trese MT
    Arch Ophthalmol; 1997 May; 115(5):651-5. PubMed ID: 9152134
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Associations of VEGF/VEGF-receptor and HGF/c-Met promoter polymorphisms with progression/regression of retinopathy of prematurity.
    Kaya M; Çokakli M; Berk AT; Yaman A; Yesilirmak D; Kumral A; Atabey N
    Curr Eye Res; 2013 Jan; 38(1):137-42. PubMed ID: 23094709
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Retinopathy of prematurity and serum level of insulin-like growth factor-1.
    Banjac L; Bokan V
    Acta Clin Croat; 2012 Jun; 51(2):209-13. PubMed ID: 23115944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The pathophysiology of retinopathy of prematurity: an update of previous and recent knowledge.
    Cavallaro G; Filippi L; Bagnoli P; La Marca G; Cristofori G; Raffaeli G; Padrini L; Araimo G; Fumagalli M; Groppo M; Dal Monte M; Osnaghi S; Fiorini P; Mosca F
    Acta Ophthalmol; 2014 Feb; 92(1):2-20. PubMed ID: 23617889
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Validation of WINROP for detecting retinopathy of prematurity in a North American cohort of preterm infants.
    Jung JL; Wagner BD; McCourt EA; Palestine AG; Cerda A; Cao JH; Enzenauer RW; Singh JK; Braverman RS; Wymore E; Lynch AM
    J AAPOS; 2017 Jun; 21(3):229-233. PubMed ID: 28506724
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Angiotensin-converting enzyme gene insertion/deletion polymorphism in Kuwaiti children with retinopathy of prematurity.
    Haider MZ; Devarajan LV; Al-Essa M; Kumar H
    Biol Neonate; 2002 Aug; 82(2):84-8. PubMed ID: 12169829
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frizzled-4 Variations Associated with Retinopathy and Intrauterine Growth Retardation: A Potential Marker for Prematurity and Retinopathy.
    Dailey WA; Gryc W; Garg PG; Drenser KA
    Ophthalmology; 2015 Sep; 122(9):1917-23. PubMed ID: 26119001
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic polymorphisms and retinopathy of prematurity.
    Cooke RW; Drury JA; Mountford R; Clark D
    Invest Ophthalmol Vis Sci; 2004 Jun; 45(6):1712-5. PubMed ID: 15161830
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.
    Hutcheson KA; Paluru PC; Bernstein SL; Koh J; Rappaport EF; Leach RA; Young TL
    Mol Vis; 2005 Jul; 11():501-8. PubMed ID: 16052165
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Endothelial nitric oxide synthase genotypes in the etiology of retinopathy of prematurity in premature infants.
    Yanamandra K; Napper D; Pramanik A; Bocchini JA; Dhanireddy R
    Ophthalmic Genet; 2010 Dec; 31(4):173-7. PubMed ID: 20809776
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.