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Journal Abstract Search

698 related items for PubMed ID: 19629903

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Ophthalmologic findings and long-term course in patients with neurofibromatosis type 2.
    Bosch MM, Boltshauser E, Harpes P, Landau K.
    Am J Ophthalmol; 2006 Jun; 141(6):1068-1077. PubMed ID: 16765675
    [Abstract] [Full Text] [Related]

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

  • 7. Neurofibromatosis type 2 associated with multiple cranial nerve schwannomas: a case report.
    Halefoğlu AM.
    Kulak Burun Bogaz Ihtis Derg; 2007 Apr; 17(3):171-5. PubMed ID: 17873509
    [Abstract] [Full Text] [Related]

  • 8. [Early type 2 neurofibromatosis and congenital retinal hamartoma].
    Hérissé AL, Poirée M, Boyer C, Soler C, Leloutre B, Geoffray A.
    Arch Pediatr; 2015 Jul; 22(7):729-32. PubMed ID: 26047750
    [Abstract] [Full Text] [Related]

  • 9. Neurofibromatosis 2: two case reports.
    Drsata J, Celakovský P, Vokurka J, Lánský M.
    Int Tinnitus J; 2003 Jul; 9(2):116-8. PubMed ID: 15106286
    [Abstract] [Full Text] [Related]

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

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. [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
    [Abstract] [Full Text] [Related]

  • 13. 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 Mar; 31(2):145-7. PubMed ID: 10743927
    [Abstract] [Full Text] [Related]

  • 14. Neurofibromatosis 2 in the pediatric age group.
    Mautner VF, Tatagiba M, Guthoff R, Samii M, Pulst SM.
    Neurosurgery; 1993 Jul; 33(1):92-6. PubMed ID: 8355853
    [Abstract] [Full Text] [Related]

  • 15. Paediatric presentation of type 2 neurofibromatosis.
    Evans DG, Birch JM, Ramsden RT.
    Arch Dis Child; 1999 Dec; 81(6):496-9. PubMed ID: 10569966
    [Abstract] [Full Text] [Related]

  • 16. Clinical and genetic significance of unilateral Lisch nodules.
    Ceuterick SD, Van Den Ende JJ, Smets RM.
    Bull Soc Belge Ophtalmol; 2005 Dec; (295):49-53. PubMed ID: 15849989
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  • 18. Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity.
    Parry DM, Eldridge R, Kaiser-Kupfer MI, Bouzas EA, Pikus A, Patronas N.
    Am J Med Genet; 1994 Oct 01; 52(4):450-61. PubMed ID: 7747758
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  • 20. 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 01; 30(6):835-41. PubMed ID: 19704365
    [Abstract] [Full Text] [Related]

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