Journal of the Peripheral Nervous System

Cover image for Vol. 17 Issue 2

June 2012

Volume 17, Issue 2

Pages 141–282

  1. RESEARCH REPORTS

    1. Top of page
    2. RESEARCH REPORTS
    3. CASE REPORTS
    4. LETTER TO THE EDITOR
    5. PROCEEDINGS
    1. Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H) (pages 141–146)

      Cécile Baudot, Clothilde Esteve, Christel Castro, Yannick Poitelon, Camille Mas, Tarik Hamadouche, Maryam El-Rajab, Nicolas Lévy, André Megarbané and Valérie Delague

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00405.x

    2. Mitochondrial loss indicates early axonal damage in small fiber neuropathies (pages 147–157)

      Jordi Casanova-Molla, Merche Morales, Glòria Garrabou, Núria Solà-Valls, Alex Soriano, Maria Calvo, Josep Maria Grau and Josep Valls-Solé

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00396.x

    3. Clinical and serological features of acute sensory ataxic neuropathy with antiganglioside antibodies (pages 158–168)

      Ricard Rojas-García, Luis Querol, Eduard Gallardo, Noemi De Luna Salva, Cándido Juarez, Mercedes Garces, Eva Fages, Carlos Casasnovas and Isabel Illa

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00407.x

    4. Amyloid-like IgM deposition neuropathy: a distinct clinico-pathologic and proteomic profiled disorder (pages 182–190)

      Juan J. Figueroa, E. Peter Bosch, P. James B. Dyck, Wolfgang Singer, Julie A. Vrana, Jason D. Theis, Ahmet Dogan and Christopher J. Klein

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00406.x

    5. Plasma homocysteine levels are independently associated with the severity of peripheral polyneuropathy in type 2 diabetic subjects (pages 191–196)

      Ricardo González, Teresa Pedro, Sergio Martinez-Hervas, Miguel Civera, Maria Antonia Priego, Miguel Catalá, F. Javier Chaves, Juan F. Ascaso, Rafael Carmena and Jose T. Real

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00408.x

  2. CASE REPORTS

    1. Top of page
    2. RESEARCH REPORTS
    3. CASE REPORTS
    4. LETTER TO THE EDITOR
    5. PROCEEDINGS
    1. Phenotypic presentation of the Ser63Del MPZ mutation (pages 197–200)

      Lindsey J. Miller, Agnes Patzko, Richard A. Lewis and Michael E. Shy

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00398.x

    2. A novel p.Glu175X premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2 (pages 201–205)

      Alexander M. Rossor, Gabrielle L. Davidson, Julian Blake, James M. Polke, Sinéad M. Murphy, Henry Houlden, Amy Innes, Bernadett Kalmar, Linda Greensmith and Mary M. Reilly

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00400.x

    3. A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease (pages 206–209)

      Kensuke Shiga, Yuichi Noto, Ikuko Mizuta, Akihiro Hashiguchi, Hiroshi Takashima and Masanori Nakagawa

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00403.x

    4. BAG3 mutations: another cause of giant axonal neuropathy (pages 210–216)

      Fatima Jaffer, Sinéad M. Murphy, Mariacristina Scoto, Estelle Healy, Alexander M. Rossor, Sebastian Brandner, Rahul Phadke, Duygu Selcen, Heinz Jungbluth, Francesco Muntoni and Mary M. Reilly

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00409.x

  3. LETTER TO THE EDITOR

    1. Top of page
    2. RESEARCH REPORTS
    3. CASE REPORTS
    4. LETTER TO THE EDITOR
    5. PROCEEDINGS
    1. BIOHYBRID – Biohybrid templates for peripheral nerve regeneration (pages 220–222)

      Claudia Grothe, Kirsten Haastert-Talini, Thomas Freier, Xavier Navarro, Lars B. Dahlin, Antonio Salgado, Shimon Rochkind, Abraham Shahar, Luis Filipe V. Pinto, Martin Hildebrandt and Stefano Geuna

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00399.x

    2. Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion (pages 223–225)

      Nicol C. Voermans, Tjitske Kleefstra, Anneke A. Gabreëls-Festen, Brigitte H. W. Faas, Erik-Jan Kamsteeg, Henry Houlden, Matilde Laurá, James M. Polke, Amelie Pandraud, Fred van Ruissen, Baziel G. van Engelen and Mary M. Reilly

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00402.x

    3. A case of multifocal motor neuropathy with conduction block associated with gastric and lung adenocarcinoma (pages 226–228)

      Andrea Rigamonti, Giuseppe Lauria, Lorenzo Stanzani, Francesca Piamarta and Elio Agostoni

      Article first published online: 27 JUN 2012 | DOI: 10.1111/j.1529-8027.2012.00401.x

  4. PROCEEDINGS

    1. Top of page
    2. RESEARCH REPORTS
    3. CASE REPORTS
    4. LETTER TO THE EDITOR
    5. PROCEEDINGS

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