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There are 442254 results for: content related to: Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsies

  1. Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2

    European Journal of Neurology

    Volume 4, Issue 3, May 1997, Pages: 274–286, A. Cruz-Martínez, S. Bort, J. Arpa, J. Duarte and F. Palau

    Article first published online : 20 JAN 2011, DOI: 10.1111/j.1468-1331.1997.tb00347.x

  2. 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

  3. Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy

    Muscle & Nerve

    Volume 21, Issue 12, December 1998, Pages: 1686–1691, Davide Pareyson, Alessandra Solari, Franco Taroni, Sara Botti, Elisa Fallica, Vidmer Scaioli, Claudia Ciano and Angelo Sghirlanzoni

    Article first published online : 12 DEC 1998, DOI: 10.1002/(SICI)1097-4598(199812)21:12<1686::AID-MUS10>3.0.CO;2-Z

  4. Lesion of the anterior branch of axillary nerve in a patient with hereditary neuropathy with liability to pressure palsies

    European Journal of Neurology

    Volume 7, Issue 5, September 2000, Pages: 577–579, S. Simonetti

    Article first published online : 25 NOV 2003, DOI: 10.1046/j.1468-1331.2000.t01-1-00121.x

  5. Bilateral hand amyotrophy with PMP-22 gene deletion

    European Journal of Neurology

    Volume 14, Issue 1, January 2007, Pages: 115–116, A. Gochard, A. M. Guennoc, J. Praline, M. C. Malinge, B. De Toffol and P. Corcia

    Article first published online : 2 NOV 2006, DOI: 10.1111/j.1468-1331.2006.01576.x

  6. Hereditary neuropathy with liability to pressure palsies associated with central nervous system myelin lesions

    European Journal of Neurology

    Volume 8, Issue 6, November 2001, Pages: 689–692, J. Dac˘ković, V. Rakoc˘ević-Stojanović, S. Pavlović, N. Zamurović, N. Dragašević, S. Romac and S. Apostolski

    Article first published online : 21 DEC 2001, DOI: 10.1046/j.1468-1331.2001.00306.x

  7. 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

  8. Fulminant case of hereditary neuropathy with liability to pressure palsy

    Muscle & Nerve

    Volume 23, Issue 6, June 2000, Pages: 979–983, Brian A. Crum, Eric J. Sorenson, Gregorio A. Abad and P. James B. Dyck

    Article first published online : 23 MAY 2000, DOI: 10.1002/(SICI)1097-4598(200006)23:6<979::AID-MUS23>3.0.CO;2-0

  9. 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

  10. 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

  11. Charcot–Marie–Tooth disease and related neuropathies: Molecular basis for distinction and diagnosis

    Muscle & Nerve

    Volume 22, Issue 11, November 1999, Pages: 1498–1509, Davide Pareyson

    Article first published online : 7 OCT 1999, DOI: 10.1002/(SICI)1097-4598(199911)22:11<1498::AID-MUS4>3.0.CO;2-9

  12. Sonographic and electrodiagnostic features of hereditary neuropathy with liability to pressure palsies

    Journal of the Peripheral Nervous System

    Volume 17, Issue 4, December 2012, Pages: 391–398, Federica Ginanneschi, Georgios Filippou, Fabio Giannini, Maria A. Carluccio, Antonella Adinolfi, Bruno Frediani, Maria T. Dotti and Alessandro Rossi

    Article first published online : 21 DEC 2012, DOI: 10.1111/j.1529-8027.2012.00437.x

  13. 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

  14. Sonographic detection of diffuse peripheral nerve enlargement in hereditary neuropathy with liability to pressure palsies

    Journal of Clinical Ultrasound

    Volume 30, Issue 7, September 2002, Pages: 433–436, Roy Beekman and Leo H. Visser

    Article first published online : 16 AUG 2002, DOI: 10.1002/jcu.10090

  15. Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion

    Muscle & Nerve

    Volume 24, Issue 9, September 2001, Pages: 1149–1155, Jon Infante, Antonio García, Onofre Combarros, José I. Mateo, José Berciano, María J. Sedano, Eduardo J. Gutiérrez-Rivas and Francesc Palau

    Article first published online : 2 AUG 2001, DOI: 10.1002/mus.1126

  16. Axonal dysfunction, dysmyelination, and conduction failure in hereditary neuropathy with liability to pressure palsies

    Muscle & Nerve

    Volume 49, Issue 6, June 2014, Pages: 858–865, Michelle A. Farrar, Susanna B. Park, Arun V. Krishnan, Matthew C. Kiernan and Cindy S.-Y. Lin

    Article first published online : 17 MAY 2014, DOI: 10.1002/mus.24085

  17. 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

  18. Overview of Hereditary Neuropathy with Liability to Pressure Palsies

    Annals of the New York Academy of Sciences

    Volume 883, Issue 1, October 1999, Pages: 14–21, PHILIP F. CHANCE

    Article first published online : 6 FEB 2006, DOI: 10.1111/j.1749-6632.1999.tb08562.x

  19. Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies

    Muscle & Nerve

    Volume 29, Issue 2, February 2004, Pages: 205–210, Jun Li, Karen Krajewski, Richard A. Lewis and Michael E. Shy

    Article first published online : 24 NOV 2003, DOI: 10.1002/mus.10521

  20. DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations

    Acta Neurologica Scandinavica

    Volume 92, Issue 4, October 1995, Pages: 313–318, P. M. Gonnaud, F. Sturtz, V. Fourbil, C. Bonnebouche, C. Tranchant, J. M. Warter, G. Chazot, B. Bady, C. Vial, A. S. Brechard and A. Vandenberghe

    Article first published online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1995.tb00135.x