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There are 14003 results for: content related to: Multiple Cutaneous Plexiform Schwannomas as Initial Presentation of Neurofibromatosis 2 in a 9-Year-Old

  1. Schwannomas and Their Pathogenesis

    Brain Pathology

    Volume 24, Issue 3, April 2014, Pages: 205–220, David A. Hilton and Clemens Oliver Hanemann

    Version of Record online : 25 FEB 2014, DOI: 10.1111/bpa.12125

  2. Clinical Manifestations of Mutations in the Neurofibromatosis Type 2 Gene in Vestibular Schwannomas (Acoustic Neuromas)

    The Laryngoscope

    Volume 108, Issue 2, February 1998, Pages: 178–189, D. Bradley Welling

    Version of Record online : 4 JAN 2009, DOI: 10.1097/00005537-199802000-00005

  3. You have free access to this content
    Consensus recommendations for current treatments and accelerating clinical trials for patients with neurofibromatosis type 2

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 24–41, Jaishri O. Blakeley, D. Gareth Evans, John Adler, Derald Brackmann, Ruihong Chen, Rosalie E. Ferner, C. Oliver Hanemann, Gordon Harris, Susan M. Huson, Abraham Jacob, Michel Kalamarides, Matthias A. Karajannis, Bruce R. Korf, Victor-Felix Mautner, Andrea I. McClatchey, Harry Miao, Scott R. Plotkin, William Slattery III, Anat O. Stemmer-Rachamimov, D. Bradley Welling, Patrick Y. Wen, Brigitte Widemann, Kim Hunter-Schaedle and Marco Giovannini

    Version of Record online : 2 DEC 2011, DOI: 10.1002/ajmg.a.34359

  4. Calpain-dependent proteolysis of NF2 protein: Involvement in schwannomas and meningiomas

    Neuropathology

    Volume 20, Issue 3, September 2000, Pages: 153–160, Yoriyoshi Kimura, Hideyuki Saya and Mitsuyoshi Nakao

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1440-1789.2000.00326.x

  5. You have free access to this content
    What's new in neurofibromatosis? Proceedings from the 2009 NF Conference: New Frontiers

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Pages: 269–283, Joseph L. Kissil, Jaishri O. Blakeley, Rosalie E. Ferner, Susan M. Huson, Michel Kalamarides, Victor-Felix Mautner, Frank McCormick, Helen Morrison, Roger Packer, Vijaya Ramesh, Nancy Ratner, Katherine A. Rauen, David A. Stevenson, Kim Hunter-Schaedle and Kathryn North

    Version of Record online : 15 JAN 2010, DOI: 10.1002/ajmg.a.33189

  6. CpG island hypermethylation of the neurofibromatosis type 2 (NF2) gene is rare in sporadic vestibular schwannomas

    Neuropathology and Applied Neurobiology

    Volume 36, Issue 6, October 2010, Pages: 505–514, P. J. Kullar, D. M. Pearson, D. S. Malley, V. P. Collins and K. Ichimura

    Version of Record online : 14 MAY 2010, DOI: 10.1111/j.1365-2990.2010.01090.x

  7. Genome-wide methylation analysis in vestibular schwannomas shows putative mechanisms of gene expression modulation and global hypomethylation at the HOX gene cluster

    Genes, Chromosomes and Cancer

    Volume 54, Issue 4, April 2015, Pages: 197–209, Miguel Torres-Martín, Luis Lassaletta, Jose M de Campos, Alberto Isla, Giovanny R. Pinto, Rommel R. Burbano, Bárbara Melendez, Javier S. Castresana and Juan A. Rey

    Version of Record online : 23 DEC 2014, DOI: 10.1002/gcc.22232

  8. Neurofibromatosis Type 2 Clinics and Genetics

    Standard Article

    eLS

    Lan Kluwe and Victor-F Mautner

    Published Online : 15 SEP 2010, DOI: 10.1002/9780470015902.a0022391

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    Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 405–416, Scott R. Plotkin, Jaishri O. Blakeley, D. Gareth Evans, C. Oliver Hanemann, Theo J.M. Hulsebos, Kim Hunter-Schaedle, Ganjam V. Kalpana, Bruce Korf, Ludwine Messiaen, Laura Papi, Nancy Ratner, Larry S. Sherman, Miriam J. Smith, Anat O. Stemmer-Rachamimov, Jeremie Vitte and Marco Giovannini

    Version of Record online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35760

  10. Further genotype – phenotype correlations in neurofibromatosis 2

    Clinical Genetics

    Volume 77, Issue 2, February 2010, Pages: 163–170, SK Selvanathan, A Shenton, R Ferner, AJ Wallace, SM Huson, RT Ramsden and DG Evans

    Version of Record online : 23 NOV 2009, DOI: 10.1111/j.1399-0004.2009.01315.x

  11. Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?

    Clinical Genetics

    Volume 71, Issue 4, April 2007, Pages: 354–358, DGR Evans, RT Ramsden, C Gokhale, N Bowers, SM Huson and A Wallace

    Version of Record online : 25 APR 2007, DOI: 10.1111/j.1399-0004.2007.00778.x

  12. Neuropathology and Molecular Genetics of Neurofibromatosis 2 and Related Tumors

    Brain Pathology

    Volume 5, Issue 2, April 1995, Pages: 163–172, David N. Louis, Vijaya Ramesh and James F. Gusella

    Version of Record online : 28 JAN 2008, DOI: 10.1111/j.1750-3639.1995.tb00590.x

  13. Genetic testing and screening of individuals at risk of NF2

    Clinical Genetics

    Volume 82, Issue 5, November 2012, Pages: 416–424, DG Evans, FL Raymond, JG Barwell and D Halliday

    Version of Record online : 16 DEC 2011, DOI: 10.1111/j.1399-0004.2011.01816.x

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    Regulation of the Neurofibromatosis 2 gene promoter expression during embryonic development

    Developmental Dynamics

    Volume 235, Issue 10, October 2006, Pages: 2771–2785, Elena M. Akhmametyeva, Maria M. Mihaylova, Huijun Luo, Sadeq Kharzai, D. Bradley Welling and Long-Sheng Chang

    Version of Record online : 7 AUG 2006, DOI: 10.1002/dvdy.20883

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    Identification of the cis-acting region in the NF2 gene promoter as a potential target for mutation and methylation-dependent silencing in schwannoma

    Genes to Cells

    Volume 6, Issue 5, May 2001, Pages: 441–454, Takeshi Kino, Hideo Takeshima, Mitsuyoshi Nakao, Toru Nishi, Keizo Yamamoto, Takahiro Kimura, Yoshiki Saito, Masato Kochi, Jun-ichi Kuratsu, Hideyuki Saya and Yukitaka Ushio

    Version of Record online : 20 DEC 2001, DOI: 10.1046/j.1365-2443.2001.00432.x

  16. Neurofibromatosis type 2 in an infant with multiple plexiform schwannomas as first symptom

    The Journal of Dermatology

    Volume 34, Issue 1, January 2007, Pages: 60–64, Takehiko MIYAKAWA, Noriaki KAMADA, Takashi KOBAYASHI, Keiko HIRANO, Katsunori FUJII, Yoshitaro SASAHARA, Yuichiro NAGAI and Hiroshi SHINKAI

    Version of Record online : 20 DEC 2006, DOI: 10.1111/j.1346-8138.2007.00218.x

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    CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapies

    American Journal of Medical Genetics Part A

    Volume 164, Issue 3, March 2014, Pages: 563–578, Brigitte C. Widemann, Maria T. Acosta, Sylvia Ammoun, Allan J. Belzberg, Andre Bernards, Jaishri Blakeley, Antony Bretscher, Karen Cichowski, D. Wade Clapp, Eva Dombi, Gareth D. Evans, Rosalie Ferner, Cristina Fernandez-Valle, Michael J. Fisher, Marco Giovannini, David H. Gutmann, C. Oliver Hanemann, Robert Hennigan, Susan Huson, David Ingram, Joe Kissil, Bruce R. Korf, Eric Legius, Roger J. Packer, Andrea I McClatchey, Frank McCormick, Kathryn North, Minja Pehrsson, Scott R. Plotkin, Vijaya Ramesh, Nancy Ratner, Susann Schirmer, Larry Sherman, Elizabeth Schorry, David Stevenson, Douglas R. Stewart, Nicole Ullrich, Annette C. Bakker and Helen Morrison

    Version of Record online : 17 JAN 2014, DOI: 10.1002/ajmg.a.36312

  18. Multiple unilateral schwannomas: segmental neurofibromatosis type 2 or schwannomatosis?

    British Journal of Dermatology

    Volume 148, Issue 4, April 2003, Pages: 804–809, M. Leverkus, L. Kluwe, E-M. Röll, G. Becker, E-B. Bröcker, V.F. Mautner and H. Hamm

    Version of Record online : 7 MAY 2003, DOI: 10.1046/j.1365-2133.2003.05249.x

  19. Neurofibromatosis type 2 in the elderly population: Clinical and molecular features

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 667–670, Stéphane Goutagny, Alpha B. Bah, Béatrice Parfait, Olivier Sterkers and Michel Kalamarides

    Version of Record online : 15 JAN 2013, DOI: 10.1002/ajmg.a.35851

  20. Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma

    Clinical Genetics

    Volume 81, Issue 1, January 2012, Pages: 82–87, B Zirn, L Arning, I Bartels, M Shoukier, S Hoffjan, B Neubauer and A Hahn

    Version of Record online : 22 DEC 2010, DOI: 10.1111/j.1399-0004.2010.01598.x