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1991 1
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23 results

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Page 1
Chronic inflammatory demyelinating polyneuropathy: update on diagnosis, immunopathogenesis and treatment.
Lehmann HC, Burke D, Kuwabara S. Lehmann HC, et al. J Neurol Neurosurg Psychiatry. 2019 Sep;90(9):981-987. doi: 10.1136/jnnp-2019-320314. Epub 2019 Apr 16. J Neurol Neurosurg Psychiatry. 2019. PMID: 30992333 Review.
However, there are several 'atypical' subtypes, such as multifocal acquired demyelinating sensory and motor neuropathy (Lewis-Sumner syndrome) and 'distal acquired demyelinating symmetric neuropathy', possibly having different immunopathogenesis and treatment …
However, there are several 'atypical' subtypes, such as multifocal acquired demyelinating sensory and motor neuropathy (Lewis-Sumn …
Lewis-sumner syndrome of pure upper-limb onset: diagnostic, prognostic, and therapeutic features.
Rajabally YA, Chavada G. Rajabally YA, et al. Muscle Nerve. 2009 Feb;39(2):206-20. doi: 10.1002/mus.21199. Muscle Nerve. 2009. PMID: 19145651 Review.
Lewis-Sumner syndrome (L-SS) represents the asymmetric variant of chronic inflammatory demyelinating polyneuropathy (CIDP). ...
Lewis-Sumner syndrome (L-SS) represents the asymmetric variant of chronic inflammatory demyelinating polyneuropathy (CI …
Inflammatory neuropathies.
Whitesell J. Whitesell J. Semin Neurol. 2010 Sep;30(4):356-64. doi: 10.1055/s-0030-1267279. Epub 2010 Oct 12. Semin Neurol. 2010. PMID: 20941668 Review.
The most common example of an acute inflammatory neuropathy is acute inflammatory demyelinating polyradiculoneuropathy (AIDP), which is part of the Guillain-Barre syndrome (GBS). The most common chronic inflammatory neuropathy is chronic inflammatory demyelinating polyradi …
The most common example of an acute inflammatory neuropathy is acute inflammatory demyelinating polyradiculoneuropathy (AIDP), which is part …
Clinical neurophysiology of demyelinating polyneuropathy.
Bowley MP, Chad DA. Bowley MP, et al. Handb Clin Neurol. 2019;161:241-268. doi: 10.1016/B978-0-444-64142-7.00052-7. Handb Clin Neurol. 2019. PMID: 31307604 Review.
They present with phenotypes that range from an indolent disorder that begins in childhood and progresses slowly over decades (as might be seen in an inherited form) and leads to weakness but preserved ambulation, to a neuropathy with fulminant onset and rapid progression culmina …
They present with phenotypes that range from an indolent disorder that begins in childhood and progresses slowly over decades (as might be s …
Atypical chronic inflammatory demyelinating polyradiculoneuropathy: recent advances on classification, diagnosis, and pathogenesis.
Doneddu PE, Dentoni M, Nobile-Orazio E. Doneddu PE, et al. Curr Opin Neurol. 2021 Oct 1;34(5):613-624. doi: 10.1097/WCO.0000000000000979. Curr Opin Neurol. 2021. PMID: 34267052 Free PMC article. Review.
Recent studies suggest that patients with typical CIDP have an antibody-mediated mechanism of neuropathy whereas in those with Lewis--Sumner syndrome (LSS) neuropathy is preferentially mediated by macrophages and T cells. ...
Recent studies suggest that patients with typical CIDP have an antibody-mediated mechanism of neuropathy whereas in those with Lewis- …
Treatment of chronic immune-mediated neuropathies: chronic inflammatory demyelinating polyradiculoneuropathy, multifocal motor neuropathy, and the Lewis-Sumner syndrome.
Sederholm BH. Sederholm BH. Semin Neurol. 2010 Sep;30(4):443-56. doi: 10.1055/s-0030-1267289. Epub 2010 Oct 12. Semin Neurol. 2010. PMID: 20941678 Review.
Current treatment approaches for the management of chronic immune-mediated peripheral neuropathies are reviewed, including chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), multifocal motor neuropathy (MMN), and the Lewis-Sumner syndrome (LSS) …
Current treatment approaches for the management of chronic immune-mediated peripheral neuropathies are reviewed, including chronic inflammat …
Acquired inflammatory demyelinating neuropathies.
Ensrud ER, Krivickas LS. Ensrud ER, et al. Phys Med Rehabil Clin N Am. 2001 May;12(2):321-34, ix. Phys Med Rehabil Clin N Am. 2001. PMID: 11345010 Review.
The acquired demyelinating neuropathies can be divided into those with an acute onset and course and those with a more chronic course. The acute neuropathies present as Guillain-Barre syndrome and include acute inflammatory demyelinating polyradiculoneuropathy (AIDP), Mill …
The acquired demyelinating neuropathies can be divided into those with an acute onset and course and those with a more chronic course. The a …
[Lewis-Sumner syndrome].
Higashi T, Tashiro K. Higashi T, et al. Ryoikibetsu Shokogun Shirizu. 2000;(31):39-43. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11269115 Review. Japanese. No abstract available.
Neuromuscular Mimics of Entrapment Neuropathies of Upper Extremities.
Gilchrist JM, Dandapat S. Gilchrist JM, et al. Hand (N Y). 2020 Sep;15(5):599-607. doi: 10.1177/1558944719898801. Epub 2020 Feb 5. Hand (N Y). 2020. PMID: 32020820 Free PMC article. Review.
Introduction: Carpal tunnel syndrome and ulnar neuropathy are such common maladies affecting the upper extremties that they often become the default diagnosis when patients complain of numbness, pain, or weakness of the hands. While often correct, there are a number of oth …
Introduction: Carpal tunnel syndrome and ulnar neuropathy are such common maladies affecting the upper extremties that they often bec …
Neuropathies associated with conduction block.
Lewis RA. Lewis RA. Curr Opin Neurol. 2007 Oct;20(5):525-30. doi: 10.1097/WCO.0b013e3282efa143. Curr Opin Neurol. 2007. PMID: 17885439 Review.
PURPOSE OF REVIEW: Two disorders, Lewis-Sumner syndrome and multifocal motor neuropathy, are defined by the demonstration of conduction block. ...Evidence suggests that Lewis-Sumner syndrome is a multifocal variant of chronic inflammatory …
PURPOSE OF REVIEW: Two disorders, Lewis-Sumner syndrome and multifocal motor neuropathy, are defined by the demonstrati …
23 results