Clinical, electrophysiological, genetic, and imaging features of six Chinese Han patients with hereditary neuropathy with liability to pressure palsies (HNPP)
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery
Reference19 articles.
1. Guidelines for diagnosis of hereditary neuropathywith liability to pressure palsies;Dubourg;Neuromuscul Disord,2000
2. Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study;Chanson;Neurol Neurosurg Psychiatry,2013
3. Hereditary neuropathy with liability to pressure palsies in childhood: case series and literature update;Chrestian;Neuromuscul Disord,2015
4. Hereditary recurrent focal neuropathies: clinical and molecular features;Stogbauer;Neurology,2000
5. Charcot-marie-tooth disease in Northern England;Foley;J Neurol Neurosurg Psychiatry,2012
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1. Multiple tendon transfer for a case of radial nerve palsy in hereditary neuropathy with liability to pressure palsy;NAGOYA J MED SCI;2023
2. Hereditary neuropathy with liability to pressure palsies misdiagnosed as Guillain–Barré Syndrome: A case report;Medicine;2022-09-23
3. Two Novel Myelin Protein Zero Mutations in a Group of Chinese Patients;Frontiers in Neurology;2021-12-02
4. A New Point Mutation in the PMP22 Gene in a Family Suffering From Atypical HNPP;Journal of Neuromuscular Diseases;2020-09-18
5. Comparison of clinical and electrophysiological features of patients with hereditary neuropathy with liability to pressure palsies with or without pain;Journal of the Neurological Sciences;2020-02
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