BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

288 related articles for article (PubMed ID: 18766994)

  • 1. Combined retinal hamartomas leading to the diagnosis of neurofibromatosis type 2.
    Grant EA; Trzupek KM; Reiss J; Crow K; Messiaen L; Weleber RG
    Ophthalmic Genet; 2008 Sep; 29(3):133-8. PubMed ID: 18766994
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bilateral combined hamartomas of the retina and retinal pigment epithelium as the presenting feature of neurofibromatosis type 2 (Wishart Type).
    Firestone BK; Arias JD; Shields CL; Shields JA
    J Pediatr Ophthalmol Strabismus; 2014; 51 Online():doi: 10.3928/01913913-20140521-02. PubMed ID: 25922868
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Combined hamartomas of the retinal pigment epithelium and retina.
    Palmer ML; Carney MD; Combs JL
    Retina; 1990; 10(1):33-6. PubMed ID: 2343189
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Infantile onset neurofibromatosis type 2 presenting with peripheral facial palsy, skin patches, retinal hamartoma and foot drop.
    Tibussek D; Hübsch S; Berger K; Schaper J; Rosenbaum T; Mayatepek E
    Klin Padiatr; 2009; 221(4):247-50. PubMed ID: 19629903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Astrocytic hamartoma of the optic disc and multiple café-au-lait macules in a child with neurofibromatosis type 2.
    Sachdeva R; Rothner DA; Traboulsi EI; Hayden BC; Rychwalski PJ
    Ophthalmic Genet; 2010 Dec; 31(4):209-14. PubMed ID: 21067482
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic significance of unilateral Lisch nodules.
    Ceuterick SD; Van Den Ende JJ; Smets RM
    Bull Soc Belge Ophtalmol; 2005; (295):49-53. PubMed ID: 15849989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Combined hamartoma of the retina and retinal pigment epithelium as the presenting sign of neurofibromatosis-1.
    Tsai P; O'Brien JM
    Ophthalmic Surg Lasers; 2000; 31(2):145-7. PubMed ID: 10743927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bilateral Combined Hamartomas of the Retina and Retinal Pigment Epithelium as the Presenting Feature of Neurofibromatosis Type 2 (Wishart Type).
    Firestone BK; Arias JD; Shields CL; Shields JA
    J Pediatr Ophthalmol Strabismus; 2014 May; 51 Online():e33-6. PubMed ID: 26900706
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients.
    Ruggieri M; Iannetti P; Polizzi A; La Mantia I; Spalice A; Giliberto O; Platania N; Gabriele AL; Albanese V; Pavone L
    Neuropediatrics; 2005 Feb; 36(1):21-34. PubMed ID: 15776319
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Retinal Astrocytic Hamartoma in Neurofibromatosis Type 2 - Metaanalysis and a Case Report].
    Starosta DA; Lorenz B
    Klin Monbl Augenheilkd; 2018 Mar; 235(3):290-300. PubMed ID: 29534265
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of bilateral, multiple presumed retinal astrocytic proliferations with combined hamartoma of retina and retinal pigment epithelium in a 9-year-old male child with neurofibromatosis type 2.
    Rishi P; Hirawat RS; Verma A
    Indian J Ophthalmol; 2016 Nov; 64(11):850-852. PubMed ID: 27958212
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epiretinal membranes indicate a severe phenotype of neurofibromatosis type 2.
    Sisk RA; Berrocal AM; Schefler AC; Dubovy SR; Bauer MS
    Retina; 2010 Apr; 30(4 Suppl):S51-8. PubMed ID: 20386093
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [NF2: ocular, neural and genetic manifestations].
    Feucht M; Mautner VF; Richard G
    Klin Monbl Augenheilkd; 2005 Apr; 222(4):312-6. PubMed ID: 15844040
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Neurofibromatosis].
    Wolkenstein P; Decq P
    Neurochirurgie; 1998 Nov; 44(4):267-72. PubMed ID: 9864698
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Nonsense mutation 193C>T of neurofibromatosis type 2--a neurosurgical challenge].
    Bobest M; Tóth C; Gyurcsó M; Molnár MJ; Garzuly F
    Ideggyogy Sz; 2007 Jan; 60(1-2):41-5. PubMed ID: 17432093
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A point mutation associated with a severe phenotype of neurofibromatosis 2.
    MacCollin M; Braverman N; Viskochil D; Ruttledge M; Davis K; Ojemann R; Gusella J; Parry DM
    Ann Neurol; 1996 Sep; 40(3):440-5. PubMed ID: 8797533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Concordance of bilateral vestibular schwannoma growth and hearing changes in neurofibromatosis 2: neurofibromatosis 2 natural history consortium.
    Fisher LM; Doherty JK; Lev MH; Slattery WH
    Otol Neurotol; 2009 Sep; 30(6):835-41. PubMed ID: 19704365
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Combined hamartoma of the retina and retinal pigment epithelium associated with neurofibromatosis type-1.
    Vianna RN; Pacheco DF; Vasconcelos MM; de Laey JJ
    Int Ophthalmol; 2001; 24(2):63-6. PubMed ID: 12201346
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Further genotype--phenotype correlations in neurofibromatosis 2.
    Selvanathan SK; Shenton A; Ferner R; Wallace AJ; Huson SM; Ramsden RT; Evans DG
    Clin Genet; 2010 Feb; 77(2):163-70. PubMed ID: 19968670
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurofibromatosis type 2 in an infant with multiple plexiform schwannomas as first symptom.
    Miyakawa T; Kamada N; Kobayashi T; Hirano K; Fujii K; Sasahara Y; Nagai Y; Shinkai H
    J Dermatol; 2007 Jan; 34(1):60-4. PubMed ID: 17204104
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.