Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies-Reference-Cited by-同舟云学术

Correlation between PMP-22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies

Published:1997-12 Issue:6 Volume:42 Page:866-872
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Schenone Angelo,Nobbio Lucilla,Caponnetto Claudia,Abbruzzese Michele,Gherardi Gianfranco,Mancardi Gianluigi,Mandich Paola,Bellone Emilia,Ajmar Franco,Windebank Anthony J.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference34 articles.

1. Inherited recurrent focal neuropathies. In: et al, eds. Peripheral neuropathy. 3rd ed. Philadelphia: WB Saunders, 1993: 1137-1148

2. DNA deletion associated with hereditary neuropathy with liability to pressure palsies

3. Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)

4. Coexpression of PMP22 gene with MBP and P0during de novo myelination and nerve repair

5. DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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1. Efficacy of Spinal Cord Stimulation Using Differential Target Multiplexed Stimulation for Intractable Pain of Hereditary Neuropathy with Liability to Pressure Palsies: A Case Report;NMC Case Report Journal;2023-12-31

2. Clinical characteristics of hereditary neuropathy with liability to pressure palsy presenting with monoparesis in the emergency department;Yeungnam University Journal of Medicine;2020-10-31

3. Elderly‐onset case of hereditary neuropathy with liability to pressure palsies: A case report;Neurology and Clinical Neuroscience;2018-07-11

4. Characterisation of pain in people with hereditary neuropathy with liability to pressure palsy;J NEUROL;2017

5. Peripheral Nerve Neuropathies Including Charcot-Marie-Tooth Disease;Neurodegeneration;2017-02-18