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Publisher: Wiley-Blackwell

Volume 17, Number 2, 1 June 2012

Two novel missense mutations in FGD4/FRABIN cause Charcot‐Marie‐Tooth type 4H (CMT4H)
pp. 141-146(6)
Authors: Baudot, Cécile; Esteve, Clothilde; Castro, Christel; Poitelon, Yannick; Mas, Camille; Hamadouche, Tarik; El‐Rajab, Maryam; Lévy, Nicolas; Megarbané, André; Delague, Valérie

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Mitochondrial loss indicates early axonal damage in small fiber neuropathies
pp. 147-157(11)
Authors: Casanova‐Molla, Jordi; Morales, Merche; Garrabou, Glòria; Solà‐Valls, Núria; Soriano, Alex; Calvo, Maria; Maria Grau, Josep; Valls‐Solé, Josep

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Clinical and serological features of acute sensory ataxic neuropathy with antiganglioside antibodies
pp. 158-168(11)
Authors: Rojas‐García, Ricard; Querol, Luis; Gallardo, Eduard; De Luna Salva, Noemi; Juarez, Cándido; Garces, Mercedes; Fages, Eva; Casasnovas, Carlos; Illa, Isabel

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Suppression of neurokinin‐1 receptor in trigeminal ganglia attenuates central sensitization following inflammation
pp. 169-181(13)
Authors: Takeda, Mamoru; Takahashi, Masayuki; Matsumoto, Shigeji

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Amyloid‐like IgM deposition neuropathy: a distinct clinico‐pathologic and proteomic profiled disorder
pp. 182-190(9)
Authors: Figueroa, Juan J.; Peter Bosch, E.; Dyck, P. James B.; Singer, Wolfgang; Vrana, Julie A.; Theis, Jason D.; Dogan, Ahmet; Klein, Christopher J.

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Plasma homocysteine levels are independently associated with the severity of peripheral polyneuropathy in type 2 diabetic subjects
pp. 191-196(6)
Authors: González, Ricardo; Pedro, Teresa; Martinez‐Hervas, Sergio; Civera, Miguel; Antonia Priego, Maria; Catalá, Miguel; Javier Chaves, F.; Ascaso, Juan F.; Carmena, Rafael; Real, Jose T.

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Phenotypic presentation of the Ser63Del MPZ mutation
pp. 197-200(4)
Authors: Miller, Lindsey J.; Patzko, Agnes; Lewis, Richard A.; Shy, Michael E.

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A novel p.Glu175X premature stop mutation in the C‐terminal end of HSP27 is a cause of CMT2
pp. 201-205(5)
Authors: Rossor, Alexander M.; Davidson, Gabrielle L.; Blake, Julian; Polke, James M.; Murphy, Sinéad M.; Houlden, Henry; Innes, Amy; Kalmar, Bernadett; Greensmith, Linda; Reilly, Mary M.

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A novel EGR2 mutation within a family with a mild demyelinating form of Charcot‐Marie‐Tooth disease
pp. 206-209(4)
Authors: Shiga, Kensuke; Noto, Yuichi; Mizuta, Ikuko; Hashiguchi, Akihiro; Takashima, Hiroshi; Nakagawa, Masanori

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BAG3 mutations: another cause of giant axonal neuropathy
pp. 210-216(7)
Authors: Jaffer, Fatima; Murphy, Sinéad M.; Scoto, Mariacristina; Healy, Estelle; Rossor, Alexander M.; Brandner, Sebastian; Phadke, Rahul; Selcen, Duygu; Jungbluth, Heinz; Muntoni, Francesco; Reilly, Mary M.

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Retrospective analysis of Slovenian patients with Guillain‐Barré syndrome
pp. 217-219(3)
Authors: Omejec, Gregor; Podnar, Simon

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BIOHYBRID – Biohybrid templates for peripheral nerve regeneration
pp. 220-222(3)
Authors: Grothe, Claudia; Haastert‐Talini, Kirsten; Freier, Thomas; Navarro, Xavier; Dahlin, Lars B.; Salgado, Antonio; Rochkind, Shimon; Shahar, Abraham; Pinto, Luis Filipe V.; Hildebrandt, Martin; Geuna, Stefano

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Severe Dejerine‐Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion
pp. 223-225(3)
Authors: Voermans, Nicol C.; Kleefstra, Tjitske; Gabreëls‐Festen, Anneke A.; Faas, Brigitte H. W.; Kamsteeg, Erik‐Jan; Houlden, Henry; Laurá, Matilde; Polke, James M.; Pandraud, Amelie; van Ruissen, Fred; van Engelen, Baziel G.; Reilly, Mary M.

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A case of multifocal motor neuropathy with conduction block associated with gastric and lung adenocarcinoma
pp. 226-228(3)
Authors: Rigamonti, Andrea; Lauria, Giuseppe; Stanzani, Lorenzo; Piamarta, Francesca; Agostoni, Elio

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