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Publisher: Wiley-Blackwell

Volume 22, Number 4, 1 December 2017

Maintenance IV immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy
pp. 425-432(8)
Authors: Kuitwaard, Krista; Fokkink, Willem‐Jan R.; Brusse, Esther; Vrancken, Alexander F. J. E.; Eftimov, Filip; Notermans, Nicolette C.; van der Kooi, Anneke J.; Merkies, Ingemar S. J.; Jacobs, Bart C.; van Doorn, Pieter A.

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Markers for Guillain‐Barré syndrome with poor prognosis: a multi‐center study
pp. 433-439(7)
Authors: Yamagishi, Yuko; Suzuki, Hidekazu; Sonoo, Masahiro; Kuwabara, Satoshi; Yokota, Takanori; Nomura, Kyoichi; Chiba, Atsuro; Kaji, Ryuji; Kanda, Takashi; Kaida, Kenichi; Ikeda, Shu‐ichi; Mutoh, Tatsuro; Yamasaki, Ryo; Takashima, Hiroshi; Matsui, Makoto; Nishiyama, Kazutoshi; Sobue, Gen; Kusunoki, Susumu

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Epidemiology of Guillain‐Barré syndrome in Finland 2004–2014
pp. 440-445(6)
Authors: Sipilä, Jussi O.T.; Soilu‐Hänninen, Merja; Ruuskanen, Jori O.; Rautava, Päivi; Kytö, Ville

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Prediction of disease progression in Miller Fisher and overlap syndromes
pp. 446-450(5)
Authors: Verboon, Christine; van Berghem, Heleen; van Doorn, Pieter A.; Ruts, Liselotte; Jacobs, Bart C.

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The role of nutrition as risk factor for polyneuropathy: a case‐control study
pp. 455-459(5)
Authors: Visser, Nora A.; Notermans, Nicolette C.; de Vries, Jeanne H. M.; van den Berg, Leonard H.; Vrancken, Alexander F. J. E.

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A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorder
pp. 460-463(4)
Authors: Tomaselli, Pedro J.; Rossor, Alexander M.; Horga, Alejandro; Laura, Matilde; Blake, Julian C.; Houlden, Henry; Reilly, Mary M.

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Pseudodominant inheritance pattern in a family with CMT2 caused by GDAP1 mutations
pp. 464-467(4)
Authors: van Paassen, Barbara W.; Bronk, Marieke; Verhamme, Camiel; van Ruissen, Fred; Baas, Frank; van Spaendonck‐Zwarts, Karin Y.; de Visser, Marianne

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