Rapidly progressive amyotrophic lateral sclerosis in a young patient with hereditary neuropathy with liability to pressure palsies-Reference-Cited by-同舟云学术

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Rapidly progressive amyotrophic lateral sclerosis in a young patient with hereditary neuropathy with liability to pressure palsies

Published:2010-01 Issue:3 Volume:11 Page:335-336
ISSN:1748-2968
Container-title:Amyotrophic Lateral Sclerosis
language:en
Short-container-title:Amyotrophic Lateral Sclerosis

Author:

Canali Elena,Chiari Annalisa,Sola Patrizia,Fioravanti Valentina,Valzania Franco,Pentore Roberta,Nichelli Paolo,Mandrioli Jessica

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/17482960902964440

Reference12 articles.

1. Tomaculous neuropathy: A clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p<11.2

2. Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

3. Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland

4. ALS in a patient with hereditary neuropathy with liability to pressure palsy

5. Hereditary neuropathy with liability to pressure palsies associated with central nervous system myelin lesions

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sensory neuropathy in amyotrophic lateral sclerosis: a systematic review;Journal of Neurology;2023-08-23

2. Thr124Met myelin protein zero mutation mimicking motor neuron disease;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2021-07-01

3. Case of hereditary neuropathy with liability to pressure palsies presenting progressive muscular atrophy with lower motor neuron degeneration in the spinal cord and the brainstem;Neurology and Clinical Neuroscience;2015-08-11

4. An autopsy case of coexisting Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyradiculoneuropathy, later associated with amyotrophic lateral sclerosis;Rinsho Shinkeigaku;2012

5. Sural nerve pathology in ALS patients: a single-centre experience;Neurological Sciences;2011-12-28

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