Search Results

There are 12573 results for: content related to: Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

  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. Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas

    Human Mutation

    Volume 29, Issue 2, February 2008, Pages: 227–231, Roberta Sestini, Costanza Bacci, Aldesia Provenzano, Maurizio Genuardi and Laura Papi

    Version of Record online : 10 DEC 2007, DOI: 10.1002/humu.20679

  3. Molecular Genetics of Schwannomatosis

    Standard Article

    eLS

    Theo JM Hulsebos

    Published Online : 15 NOV 2017, DOI: 10.1002/9780470015902.a0021427.pub2

  4. SWI/SNF chromatin remodeling complexes and cancer

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 166, Issue 3, September 2014, Pages: 350–366, Jaclyn A. Biegel, Tracy M. Busse and Bernard E. Weissman

    Version of Record online : 28 AUG 2014, DOI: 10.1002/ajmg.c.31410

  5. Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

    Clinical Genetics

    Volume 74, Issue 4, October 2008, Pages: 358–366, C Boyd, MJ Smith, L Kluwe, A Balogh, M MacCollin and SR Plotkin

    Version of Record online : 21 JUL 2008, DOI: 10.1111/j.1399-0004.2008.01060.x

  6. Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cells

    Genes, Chromosomes and Cancer

    Volume 55, Issue 4, April 2016, Pages: 350–354, Theo J.M. Hulsebos, Susan Kenter, Frank Baas, Eline A. Nannenberg, Fonnet E. Bleeker, Rick van Minkelen, Ans M.W. van den Ouweland, Pieter Wesseling and Uta Flucke

    Version of Record online : 22 JAN 2016, DOI: 10.1002/gcc.22338

  7. Immunohistochemical Analysis Supports a Role for INI1/SMARCB1 in Hereditary Forms of Schwannomas, but Not in Solitary, Sporadic Schwannomas

    Brain Pathology

    Volume 18, Issue 4, October 2008, Pages: 517–519, Sushama Patil, Arie Perry, Mia MacCollin, Shumin Dong, Rebecca A. Betensky, Tu-Hsueh Yeh, David H. Gutmann and Anat O. Stemmer-Rachamimov

    Version of Record online : 15 APR 2008, DOI: 10.1111/j.1750-3639.2008.00155.x

  8. You have full text access to this OnlineOpen article
    Oncogenic roles of SMARCB1/INI1 and its deficient tumors

    Cancer Science

    Volume 108, Issue 4, April 2017, Pages: 547–552, Kenichi Kohashi and Yoshinao Oda

    Version of Record online : 12 APR 2017, DOI: 10.1111/cas.13173

  9. 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

  10. Use of clinical next-generation sequencing to identify melanomas harboring SMARCB1 mutations

    Journal of Cutaneous Pathology

    Volume 42, Issue 5, May 2015, Pages: 308–317, David L. Stockman, Jonathan L. Curry, Carlos A. Torres-Cabala, Ian R. Watson, Alan E. Siroy, Roland L. Bassett, Lihua Zou, Keyur P. Patel, Rajyalakshmi Luthra, Michael A. Davies, Jennifer A. Wargo, Mark A. Routbort, Russell R. Broaddus, Victor G. Prieto, Alexander J. Lazar and Michael T. Tetzlaff

    Version of Record online : 24 MAR 2015, DOI: 10.1111/cup.12481

  11. Genetic insights into familial tumors of the nervous system

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 129C, Issue 1, 15 August 2004, Pages: 74–84, German Melean, Roberta Sestini, Franco Ammannati and Laura Papi

    Version of Record online : 6 JUL 2004, DOI: 10.1002/ajmg.c.30022

  12. Frequent co-inactivation of the SWI/SNF subunits SMARCB1, SMARCA2 and PBRM1 in malignant rhabdoid tumours

    Histopathology

    Volume 67, Issue 1, July 2015, Pages: 121–129, Qiu Rao, Qiu-yuan Xia, Zi-yu Wang, Li Li, Qin Shen, Shan-shan Shi, Xuan Wang, Biao Liu, Yan-fen Wang, Qun-li Shi, Heng-hui Ma, Zhen-feng Lu, Yan He, Ru-song Zhang, Bo Yu and Xiao-jun Zhou

    Version of Record online : 5 FEB 2015, DOI: 10.1111/his.12632

  13. SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis

    Clinical Genetics

    Volume 77, Issue 1, January 2010, Pages: 86–91, TJM Hulsebos, SB Kenter, ME Jakobs, F Baas, B Chong and MB Delatycki

    Version of Record online : 11 NOV 2009, DOI: 10.1111/j.1399-0004.2009.01249.x

  14. Report of a patient with a constitutional missense mutation in SMARCB1, Coffin–Siris phenotype, and schwannomatosis

    American Journal of Medical Genetics Part A

    Volume 167, Issue 12, December 2015, Pages: 3186–3191, Nathan Gossai, Jaclyn A. Biegel, Ludwine Messiaen, Susan A. Berry and Christopher L. Moertel

    Version of Record online : 14 SEP 2015, DOI: 10.1002/ajmg.a.37356

  15. Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 215–219, Miriam J. Smith, Anjana Kulkarni, Cecilie Rustad, Naomi L. Bowers, Andrew J. Wallace, Susan E. Holder, Arvid Heiberg, Richard T. Ramsden and D. Gareth Evans

    Version of Record online : 21 NOV 2011, DOI: 10.1002/ajmg.a.34376

  16. You have free access to this content
    Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors

    Pediatric Blood & Cancer

    Volume 56, Issue 1, January 2011, Pages: 7–15, Katherine W. Eaton, Laura S. Tooke, Luanne M. Wainwright, Alexander R. Judkins and Jaclyn A. Biegel

    Version of Record online : 24 NOV 2010, DOI: 10.1002/pbc.22831

  17. Creation of an international registry to support discovery in schwannomatosis

    American Journal of Medical Genetics Part A

    Volume 173, Issue 2, February 2017, Pages: 407–413, K. L. Ostrow, A. L. Bergner, J. Blakeley, D. G. Evans, R. Ferner, J. M. Friedman, G. J. Harris, J. T. Jordan, B. Korf, S. Langmead, G. Leschziner, V. Mautner, V. L. Merker, L. Papi, S. R. Plotkin, J. M. Slopis, M. J. Smith, A. Stemmer-Rachamimov, K. Yohay and A. J. Belzberg

    Version of Record online : 19 OCT 2016, DOI: 10.1002/ajmg.a.38024

  18. Syndrome-associated soft tissue tumours

    Histopathology

    Volume 64, Issue 1, January 2014, Pages: 68–87, Cheryl M Coffin, Jessica L Davis and Scott C Borinstein

    Version of Record online : 18 NOV 2013, DOI: 10.1111/his.12280

  19. Glial papillary tumour of the spinal cord with SMARCB1/INI1-loss and favourable long-term outcome

    Neuropathology and Applied Neurobiology

    Accepted manuscript online: 20 FEB 2017, Martin Hasselblatt, Anastasia Dewi Kurniawan, Stephanie Rozsnoki, Pascal D. Johann, Susanne Bens, Florian Oyen, Reinhard Schneppenheim, Reiner Siebert, David Capper, Marcel Kool, Christoph Schul and Werner Paulus

    DOI: 10.1111/nan.12395

  20. Multifocal nerve lesions and LZTR1 germline mutations in segmental schwannomatosis

    Annals of Neurology

    Volume 80, Issue 4, October 2016, Pages: 625–628, Said Farschtschi, Victor-Felix Mautner, Mirko Pham, Rosa Nguyen, Hildegard Kehrer-Sawatzki, Sonja Hutter, Reinhard E. Friedrich, Alexander Schulz, Helen Morrison, David T. W. Jones, Martin Bendszus and Philipp Bäumer

    Version of Record online : 13 AUG 2016, DOI: 10.1002/ana.24753