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 *

129 related articles for article (PubMed ID: 20385941)

  • 21. Clinical and genetic analysis of Indian patients with NDP-related retinopathies.
    Sudha D; Ganapathy A; Mohan P; Mannan AU; Krishna S; Neriyanuri S; Swaminathan M; Rishi P; Chidambaram S; Arunachalam JP
    Int Ophthalmol; 2018 Jun; 38(3):1251-1260. PubMed ID: 28602015
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Outcome of eyes developing retinal detachment during the Early Treatment for Retinopathy of Prematurity Study (ETROP).
    Repka MX; Tung B; Good WV; Shapiro M; Capone A; Baker JD; Barr CC; Phelps DL; van Heuven WA
    Arch Ophthalmol; 2006 Jan; 124(1):24-30. PubMed ID: 16401781
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Surgical results of persistent hyperplastic primary vitreous.
    Dass AB; Trese MT
    Ophthalmology; 1999 Feb; 106(2):280-4. PubMed ID: 9951477
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Ocular phenotypes associated with two mutations (R121W, C126X) in the Norrie disease gene.
    Kellner U; Fuchs S; Bornfeld N; Foerster MH; Gal A
    Ophthalmic Genet; 1996 Jun; 17(2):67-74. PubMed ID: 8832723
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prognostic factors in open eye injury managed with vitrectomy: retrospective study.
    Globocnik Petrovic M; Lumi X; Drnovsek Olup B
    Croat Med J; 2004 Jun; 45(3):299-303. PubMed ID: 15185422
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Bilateral persistent fetal vasculature due to a mutation in the Norrie disease protein gene.
    Payabvash S; Anderson JS; Nascene DR
    Neuroradiol J; 2015 Dec; 28(6):623-7. PubMed ID: 26459204
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease.
    Andarva M; Jamshidi J; Ghaedi H; Daftarian N; Emamalizadeh B; Alehabib E; Taghavi S; Pouriran R; Darvish H
    Clin Exp Optom; 2018 Mar; 101(2):255-259. PubMed ID: 28922694
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathy.
    Shastry BS
    Biochem Biophys Res Commun; 1998 May; 246(1):35-8. PubMed ID: 9618247
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [A literature review of Norrie disease].
    Ohba N; Isashiki Y
    Nippon Ganka Gakkai Zasshi; 1996 Feb; 100(2):101-10. PubMed ID: 8851148
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel missense Norrie disease mutation associated with a severe ocular phenotype.
    Khan AO; Shamsi FA; Al-Saif A; Kambouris M
    J Pediatr Ophthalmol Strabismus; 2004; 41(6):361-3. PubMed ID: 15609522
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
    Sandberg MA; Rosner B; Weigel-DiFranco C; Dryja TP; Berson EL
    Invest Ophthalmol Vis Sci; 2007 Mar; 48(3):1298-304. PubMed ID: 17325176
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pars plana lensectomy, pars plana vitrectomy, and silicone oil tamponade as initial management of cataract and combined traction/rhegmatogenous retinal detachment involving the macula associated with severe proliferative diabetic retinopathy.
    Douglas MJ; Scott IU; Flynn HW
    Ophthalmic Surg Lasers Imaging; 2003; 34(4):270-8. PubMed ID: 12875454
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Inversion (X)(p11.4q22) associated with Norrie disease in a four generation family.
    Pettenati MJ; Rao PN; Weaver RG; Thomas IT; McMahan MR
    Am J Med Genet; 1993 Mar; 45(5):577-80. PubMed ID: 8456827
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The importance of biochemical and genetic findings in the diagnosis of atypical Norrie disease.
    Rodríguez-Muñoz A; García-García G; Menor F; Millán JM; Tomás-Vila M; Jaijo T
    Clin Chem Lab Med; 2018 Jan; 56(2):229-235. PubMed ID: 28742514
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Combined pars plana lensectomy-vitrectomy with open-loop flexible anterior chamber intraocular lens (AC IOL) implantation for subluxated lenses.
    Kazemi S; Wirostko WJ; Sinha S; Mieler WF; Koenig SB; Sheth BP
    Trans Am Ophthalmol Soc; 2000; 98():247-51; discussion 251-3. PubMed ID: 11190027
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Differential diagnosis of Norrie disease and X-linked familial exudative vitreoretinopathy (XL-FEVR) based on clinical and molecular evaluation.
    Wawrocka A; Niedziela Z; Skorczyk-Werner A; Krawczynski MR
    Klin Oczna; 2016; 118(3):231-4. PubMed ID: 30088388
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Risk factors for postoperative complications in lensectomy-vitrectomy with or without intraocular lens placement in ectopia lentis associated with Marfan syndrome.
    Fan F; Luo Y; Liu X; Lu Y; Zheng T
    Br J Ophthalmol; 2014 Oct; 98(10):1338-42. PubMed ID: 24831716
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hereditary subluxated lenses: visual performances and long-term follow-up after surgery.
    Anteby I; Isaac M; BenEzra D
    Ophthalmology; 2003 Jul; 110(7):1344-8. PubMed ID: 12867389
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Long-term visual outcomes following lens-sparing vitrectomy for retinopathy of prematurity.
    Singh R; Reddy DM; Barkmeier AJ; Holz ER; Ram R; Carvounis PE
    Br J Ophthalmol; 2012 Nov; 96(11):1395-8. PubMed ID: 22923456
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial cases of Norrie disease detected by copy number analysis.
    Arai E; Fujimaki T; Yanagawa A; Fujiki K; Yokoyama T; Okumura A; Shimizu T; Murakami A
    Jpn J Ophthalmol; 2014 Sep; 58(5):448-54. PubMed ID: 25023092
    [TBL] [Abstract][Full Text] [Related]  

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