Nerve conduction velocity in CMT 1A: what else can we tell?-Reference-Cited by-同舟云学术

Nerve conduction velocity in CMT 1A: what else can we tell?

Published:2016-07-14 Issue:10 Volume:23 Page:1566-1571
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Manganelli F.¹,Pisciotta C.¹,Reilly M. M.²,Tozza S.¹,Schenone A.³,Fabrizi G. M.⁴,Cavallaro T.⁵,Vita G.⁶,Padua L.⁷⁸,Gemignani F.⁹,Laurà M.²,Hughes R. A. C.²,Solari A.¹⁰,Pareyson D.¹⁰,Santoro L.¹,Nolano Maria,Iodice Rosa,Grandis Marina,Cabrini Ilaria,Bertolasi Laura,Mazzeo Anna,Majorana Giovanni,Vitetta Francesca,Scaioli Vidmer,Ciano Claudia,Calabrese Daniela,Quattrone Aldo,Blake Julian,

Affiliation:

1. Department of Neurosciences, Reproductive Sciences and Odontostomatology University Federico II of Naples Naples Italy

2. MRC Centre for Neuromuscular Diseases Institute of Neurology University College London London UK

3. Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences University of Genoa GenoaItaly

4. Department of Neuroscience, Biomedicine and Movement Sciences University of Verona VeronaItaly

5. Department of Neuroscience AOUI VeronaItaly

6. Department of Clinical and Experimental Medicine School of Neurosciences University of Messina MessinaItaly

7. Department of Geriatrics, Neurosciences and Orthopaedics Università Cattolica del Sacro Cuore RomeItaly

8. Don Carlo Gnocchi Foundation MilanItaly

9. Department of Neurosciences University of Parma ParmaItaly

10. Carlo Besta Neurological Institute IRCCS Foundation Milan Italy

Funder

Telethon

Muscular Dystrophy UK

Department of Health's National Institute for Health Research Biomedical Research Centres funding scheme

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.13079

Reference25 articles.

1. Hereditary Motor and Sensory Neuropathies: An Overview of Clinical, Genetic, Electrophysiologic, and Pathologic Features

2. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

3. Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A

4. Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: A longitudinal clinical and electrophysiologic study

5. Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot–Marie–Tooth disease 1A duplication

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