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Publisher: Wiley-Blackwell

Volume 21, Number 1, 1 March 2016

“Red‐flag” symptom clusters in transthyretin familial amyloid polyneuropathy
pp. 5-9(5)
Authors: Conceição, Isabel; González‐Duarte, Alejandra; Obici, Laura; Schmidt, Hartmut H.‐J.; Simoneau, Damien; Ong, Moh‐Lim; Amass, Leslie

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Long‐term efficacy of rituximab in IgM anti‐myelin‐associated glycoprotein neuropathy: RIMAG follow‐up study
pp. 10-14(5)
Authors: Iancu Ferfoglia, Ruxandra; Guimarães‐Costa, Raquel; Viala, Karine; Musset, Lucile; Neil, Jean; Marin, Benoit; Léger, Jean‐Marc

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Small and large fiber neuropathy in those with type 1 and type 2 diabetes: a 5‐year follow‐up study
pp. 15-21(7)
Authors: Løseth, Sissel; Stålberg, Erik V.; Lindal, Sigurd; Olsen, Edel; Jorde, Rolf; Mellgren, Svein I.

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Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?
pp. 22-26(5)
Authors: Potulska‐Chromik, Anna; Ryniewicz, Barbara; Aragon‐Gawinska, Karolina; Kabzinska, Dagmara; Seroka, Andrzej; Lipowska, Marta; Kaminska, Anna M.; Kostera‐Pruszczyk, Anna

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Cerebrospinal fluid profile and seroprevalence of antiganglioside reactivity in patients with neuralgic amyotrophy
pp. 27-32(6)
Authors: Stich, Oliver; Glos, Daniela; Brendle, Marie; Dersch, Rick; Rauer, Sebastian

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A proposed dosing algorithm for the individualized dosing of human immunoglobulin in chronic inflammatory neuropathies
pp. 33-37(5)
Authors: Lunn, Michael P.; Ellis, Lauren; Hadden, Robert D.; Rajabally, Yusuf A.; Winer, John B.; Reilly, Mary M.

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MFN2‐related genetic and clinical features in a cohort of Chinese CMT2 patients
pp. 38-44(7)
Authors: Xie, Yongzhi; Li, Xiaobo; Liu, Lei; Hu, Zhengmao; Huang, Shunxiang; Zhan, Yajin; Zi, Xiaohong; Xia, Kun; Tang, Beisha; Zhang, Ruxu

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X‐linked Charcot‐Marie‐Tooth disease type 6 (CMTX6) patients with a p.R158H mutation in the pyruvate dehydrogenase kinase isoenzyme 3 gene
pp. 45-51(7)
Authors: Kennerson, Marina L.; Kim, Eun J.; Siddell, Anna; Kidambi, Aditi; Kim, Sung M.; Hong, Young B.; Hwang, Sun H.; Chung, Ki W.; Choi, Byung‐Ok

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Semi‐dominant mutations in MFN2‐related neuropathy and implications for genetic counselling
pp. 52-54(3)
Authors: Tomaselli, Pedro J.; Rossor, Alexander M.; Polke, James M.; Poh, Roy; Blake, Julian; Reilly, Mary M.

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Erratum
pp. 55-55(1)

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