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There are 31845 results for: content related to: Bilateral hand amyotrophy with PMP-22 gene deletion

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  1. Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

    Annals of Neurology

    Volume 42, Issue 6, December 1997, Pages: 866–872, Dr. Angelo Schenone, Lucilla Nobbio, Claudia Caponnetto, Michele Abbruzzese, Gianfranco Gherardi, Gianluigi Mancardi, Paola Mandich, Emilia Bellone, Franco Ajmar and Anthony J. Windebank

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410420607

  2. Peripheral Myelin Protein-22 is Expressed in Rat and Mouse Brain and Spinal Cord Motoneurons

    European Journal of Neuroscience

    Volume 7, Issue 5, May 1995, Pages: 1080–1088, E. Parmantier, F. Cabon, C. Braun, D. D'Urso, H. W. Müller and B. Zalc

    Article first published online : 7 APR 2006, DOI: 10.1111/j.1460-9568.1995.tb01095.x

  3. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A

    Annals of Neurology

    Volume 35, Issue 4, April 1994, Pages: 445–450, Dr. Hiroo Yoshikawa, Tomoya Nishimura, Yuji Nakatsuji, Harutoshi Fujimura, Masato Himoro, Kiyoshi Hayasaka, Saburo Sakoda and Takehiko Yanagihara

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410350412

  4. Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies

    Annals of Neurology

    Volume 36, Issue 4, October 1994, Pages: 650–655, Dr. E. C. M. Mariman, A. A. W. M. Gabreëls-Festen, S. E. C. van Beersum, L. J. Valentijn, F. Baas, P. A. Bolhuis, P. J. H. Jongen, H. H. Ropers and F. J. M. Gabreëls

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410360415

  5. The 17p11.2 locus in hereditary neuropathy with liability to pressure palsies, in juvenile and familial carpal tunnel syndrome and in hereditary neuralgic amyotrophy

    European Journal of Neurology

    Volume 3, Issue 6, November 1996, Pages: 588–593, J. Kownacki, J. V. Fellenberg, K. Rösier, V. Schneider, T. Bettecken, H. Moser and J.-M. Burgunder

    Article first published online : 20 JAN 2011, DOI: 10.1111/j.1468-1331.1996.tb00277.x

  6. Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication

    Muscle & Nerve

    Volume 18, Issue 6, June 1995, Pages: 628–635, Dr. Antonio Uncini, Dr. Giovanni Di Guglielmo, Dr. Antonio Di Muzio, Dr. Domenico Gambi, Dr. Mario Sabatelli, Dr. Teresa Mignogna, Dr. Pietro Tonali, Dr. Rosalia Marzella, Dr. Palma Finelli, Dr. Nicoletta Archidiacono and Dr. Mariano Rocchi

    Article first published online : 13 OCT 2004, DOI: 10.1002/mus.880180610

  7. PMP-22 expression in the central nervous system of the embryonic mouse defines potential transverse segments and longitudinal columns

    Journal of Comparative Neurology

    Volume 378, Issue 2, 10 February 1997, Pages: 159–172, Eric Parmantier, Christine Braun, Jean-Léon Thomas, Fabienne Peyron, Salvador Martinez and Bernard Zalc

    Article first published online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-9861(19970210)378:2<159::AID-CNE1>3.0.CO;2-2

  8. The pathology of Charcot-Marie-Tooth disease and related disorders

    Neuropathology and Applied Neurobiology

    Volume 22, Issue 4, August 1996, Pages: 269–284, P. K. Thomas, R. H. M. King, J. R. Small and A. M. Robertson

    Article first published online : 12 MAY 2008, DOI: 10.1111/j.1365-2990.1996.tb01105.x

  9. Widespread expression of the peripheral myelin protein-22 gene (pmp22) in neural and non-neural tissues during murine development

    Journal of Neuroscience Research

    Volume 42, Issue 6, 15 December 1995, Pages: 733–741, D. Baechner, T. Liehr, H. Hameister, H. Altenberger, H. Grehl, U. Suter and Dr. B. Rautenstrauss

    Article first published online : 11 OCT 2004, DOI: 10.1002/jnr.490420602

  10. Hereditary neuropathy with liability to pressure palsies: Association with central nervous system demyelination

    Muscle & Nerve

    Volume 19, Issue 6, June 1996, Pages: 770–773, Anthony A. Amato and Richard J. Barohn

    Article first published online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4598(199606)19:6<770::AID-MUS13>3.0.CO;2-P

  11. Tomaculous neuropathy: A clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p<11.2

    Muscle & Nerve

    Volume 19, Issue 1, January 1996, Pages: 16–22, Anthony A. Amato, Gary S. Gronseth, Kevin J. Callerame, Kathleen S. Kagan-Hallet, Wilson W. Bryan and Richard J. Barohn

    Article first published online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4598(199601)19:1<16::AID-MUS3>3.0.CO;2-B

  12. Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies

    Muscle & Nerve

    Volume 24, Issue 8, August 2001, Pages: 1093–1096, Kristin Ørstavik, Mona Skard Heier, Peter Young and Florian Stögbauer

    Article first published online : 29 JUN 2001, DOI: 10.1002/mus.1116

  13. Neuropathic scapuloperoneal syndrome (Davidenkow's syndrome) with chromosome 17p11.2 deletion

    Muscle & Nerve

    Volume 32, Issue 5, November 2005, Pages: 668–671, Ashok Verma

    Article first published online : 8 JUL 2005, DOI: 10.1002/mus.20402

  14. Many facets of the peripheral myelin protein PMP22 in myelination and disease

    Microscopy Research and Technique

    Volume 41, Issue 5, 1 June 1998, Pages: 359–371, Roland Naef and Ueli Suter

    Article first published online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-0029(19980601)41:5<359::AID-JEMT3>3.0.CO;2-L

  15. Recurrent polyradiculoneuropathy with the 17p11.2 deletion

    Muscle & Nerve

    Volume 20, Issue 9, September 1997, Pages: 1184–1186, Nadine Le Forestier, Eric LeGuern, Philippe Coullin, Nazha Birouk, Thierry Maisonobe, Alexis Brice, Jean Marc Léger and Pierre Bouche

    Article first published online : 7 DEC 1998, DOI: 10.1002/(SICI)1097-4598(199709)20:9<1184::AID-MUS16>3.0.CO;2-T

  16. SR13/PMP-22 expression in rat nervous system, in PC12 cells, and C6 glial cell lines

    Journal of Neuroscience Research

    Volume 38, Issue 2, 1 June 1994, Pages: 167–181, Dr. M. De León, R. L. Nahin, M. E. Mendoza and M. A. Ruda

    Article first published online : 11 OCT 2004, DOI: 10.1002/jnr.490380207

  17. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies

    Annals of Neurology

    Volume 35, Issue 6, June 1994, Pages: 704–708, D. Verhalle, A. Löfgren, E. Nelis, I. Dehaene, P. Theys, M. Lammens, R. Dom, C. Van Broeckhoven and Dr. W. Robberecht

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410350611

  18. Deletions of chromosome 17p11.2 in multifocal neuropathies

    Annals of Neurology

    Volume 39, Issue 2, February 1996, Pages: 180–186, J. Tyson, Dr. S. Malcolm, P. K. Thomas and A. E. Harding

    Article first published online : 8 OCT 2004, DOI: 10.1002/ana.410390207

  19. Peripheral Neuropathies

    Brain Pathology

    Volume 7, Issue 4, October 1997, Pages: 1299–1302,

    Article first published online : 28 JAN 2008, DOI: 10.1111/j.1750-3639.1997.tb01035.x

  20. Immunoreactivity of PMP-22, P0, and other 19 to 28 kDa glycoprotens in peripheral nerve myelin of mammals and fish with HNK1 and related antibodies

    Journal of Neuroscience Research

    Volume 35, Issue 5, 1 August 1993, Pages: 546–558, Dr. J. A. Hammer, D. J. O'Shannessy, M. De Leon, R. Gould, D. Zand, G. Daune and R. H. Quarles

    Article first published online : 11 OCT 2004, DOI: 10.1002/jnr.490350511

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