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Recurrent sensory and motor neuropathy.

作者信息

Geranmayeh Fatemeh, Pritchard Jane, Janssen John C

机构信息

Department of Neurology, Chelsea and Westminster Hospital, London, UK.

出版信息

Pract Neurol. 2012 Aug;12(4):253-6. doi: 10.1136/practneurol-2011-000100.

DOI:10.1136/practneurol-2011-000100

PMID:22869770

Abstract

摘要

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Recurrent sensory and motor neuropathy.

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Recurrent sensory and motor neuropathy.

作者信息

Geranmayeh Fatemeh, Pritchard Jane, Janssen John C

机构信息

Department of Neurology, Chelsea and Westminster Hospital, London, UK.

出版信息

Pract Neurol. 2012 Aug;12(4):253-6. doi: 10.1136/practneurol-2011-000100.

DOI:10.1136/practneurol-2011-000100

PMID:22869770

Abstract

摘要

相似文献

Recurrent sensory and motor neuropathy.

Pract Neurol. 2012 Aug;12(4):253-6. doi: 10.1136/practneurol-2011-000100.

Hereditary neuropathy with liability to pressure palsies. Diagnosis in the first family (1947) confirmed.

J Peripher Nerv Syst. 2012 Dec;17(4):412-3. doi: 10.1111/j.1529-8027.2012.00440.x.

Hereditary neuropathy with liability to pressure palsy: a brief review with a case report.

Int J Neurosci. 2012 Mar;122(3):119-23. doi: 10.3109/00207454.2011.633719. Epub 2011 Nov 30.

Four novel point mutations in the PMP22 gene with phenotypes of HNPP and Dejerine-Sottas neuropathy.

Muscle Nerve. 2011 Nov;44(5):819-22. doi: 10.1002/mus.22189.

Hereditary neuropathy with liability to pressure palsies occurring during military training.

J R Army Med Corps. 2012 Mar;158(1):47-9. doi: 10.1136/jramc-158-01-12.

Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.

Neuromuscul Disord. 2014 Jan;24(1):56-62. doi: 10.1016/j.nmd.2013.09.005. Epub 2013 Sep 13.

Bell's palsy and hereditary neuropathy with liability to pressure palsy (HNPP): is there a common genetic background?

J Clin Neurosci. 2013 Jul;20(7):1042. doi: 10.1016/j.jocn.2012.10.017. Epub 2013 Apr 29.

Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.

J Clin Neuromuscul Dis. 2013 Sep;15(1):28-33. doi: 10.1097/CND.0b013e31829e22fe.

Asymptomatic Retinal Vein Occlusion in a 13-Year-Old With Heterozygous Deletion of the PMP22 Gene and a Diagnosis of Hereditary Neuropathy With Liability to Pressure Palsies.

J Neuroophthalmol. 2022 Mar 1;42(1):e367-e370. doi: 10.1097/WNO.0000000000001233. Epub 2021 Apr 14.

Coexistence of transthyretin familial amyloid polyneuropathy and hereditary neuropathy with liability to pressure palsy.

Clin Neurol Neurosurg. 2012 Dec;114(10):1355-7. doi: 10.1016/j.clineuro.2012.03.023. Epub 2012 Apr 20.