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Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia

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Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia. / Emsley, Hedley C. A.; Molloy, Jane.
In: Clinical Neurology and Neurosurgery, Vol. 105, No. 1, 12.2002, p. 23-26.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Emsley, HCA & Molloy, J 2002, 'Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia', Clinical Neurology and Neurosurgery, vol. 105, no. 1, pp. 23-26. https://doi.org/10.1016/S0303-8467(02)00087-2

APA

Emsley, H. C. A., & Molloy, J. (2002). Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia. Clinical Neurology and Neurosurgery, 105(1), 23-26. https://doi.org/10.1016/S0303-8467(02)00087-2

Vancouver

Emsley HCA, Molloy J. Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia. Clinical Neurology and Neurosurgery. 2002 Dec;105(1):23-26. Epub 2002 Oct 17. doi: 10.1016/S0303-8467(02)00087-2

Author

Emsley, Hedley C. A. ; Molloy, Jane. / Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia. In: Clinical Neurology and Neurosurgery. 2002 ; Vol. 105, No. 1. pp. 23-26.

Bibtex

@article{44549f742e6546889075d0ee87696fec,
title = "Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia",
abstract = "A 66-year-old man with secondary progressive multiple sclerosis presented with a flaccid areflexic tetraparesis evolving over a 6-week period. Clinical examination and subsequent investigation confirmed a diagnosis of sub-acute inflammatory demyelinating polyradiculoneuropathy (sub-acute IDP). Nephrotic-range proteinuria and thrombocytopaenia were also noted at the time of presentation - histopathological investigation of the former showed membranous glomerulonephritis as the basis for the protein loss. The IDP, glomerulonephritis and thrombocytopaenia recovered over the same time course. There have been previous reports of either glomerulonephritis or thrombocytopaenia occurring in association with IDP - there are no such reports of all three conditions occurring and resolving simultaneously. ",
keywords = "Glomerulonephritis, Inflammatory demyelinating polyradiculoneuropathy, Membranous thrombocytopaenia",
author = "Emsley, {Hedley C. A.} and Jane Molloy",
year = "2002",
month = dec,
doi = "10.1016/S0303-8467(02)00087-2",
language = "English",
volume = "105",
pages = "23--26",
journal = "Clinical Neurology and Neurosurgery",
issn = "0303-8467",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Inflammatory demyelinating polyradiculoneuropathy associated with membranous glomerulonephritis and thrombocytopaenia

AU - Emsley, Hedley C. A.

AU - Molloy, Jane

PY - 2002/12

Y1 - 2002/12

N2 - A 66-year-old man with secondary progressive multiple sclerosis presented with a flaccid areflexic tetraparesis evolving over a 6-week period. Clinical examination and subsequent investigation confirmed a diagnosis of sub-acute inflammatory demyelinating polyradiculoneuropathy (sub-acute IDP). Nephrotic-range proteinuria and thrombocytopaenia were also noted at the time of presentation - histopathological investigation of the former showed membranous glomerulonephritis as the basis for the protein loss. The IDP, glomerulonephritis and thrombocytopaenia recovered over the same time course. There have been previous reports of either glomerulonephritis or thrombocytopaenia occurring in association with IDP - there are no such reports of all three conditions occurring and resolving simultaneously. 

AB - A 66-year-old man with secondary progressive multiple sclerosis presented with a flaccid areflexic tetraparesis evolving over a 6-week period. Clinical examination and subsequent investigation confirmed a diagnosis of sub-acute inflammatory demyelinating polyradiculoneuropathy (sub-acute IDP). Nephrotic-range proteinuria and thrombocytopaenia were also noted at the time of presentation - histopathological investigation of the former showed membranous glomerulonephritis as the basis for the protein loss. The IDP, glomerulonephritis and thrombocytopaenia recovered over the same time course. There have been previous reports of either glomerulonephritis or thrombocytopaenia occurring in association with IDP - there are no such reports of all three conditions occurring and resolving simultaneously. 

KW - Glomerulonephritis

KW - Inflammatory demyelinating polyradiculoneuropathy

KW - Membranous thrombocytopaenia

U2 - 10.1016/S0303-8467(02)00087-2

DO - 10.1016/S0303-8467(02)00087-2

M3 - Journal article

C2 - 12445919

AN - SCOPUS:0036891017

VL - 105

SP - 23

EP - 26

JO - Clinical Neurology and Neurosurgery

JF - Clinical Neurology and Neurosurgery

SN - 0303-8467

IS - 1

ER -