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of 247
pro vyhledávání: '"Norman Latov"'
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 06, Pp 001-007 (2024)
Background Patients with anti-MAG neuropathy present with distal demyelinating polyneuropathy, IgM monoclonal gammopathy, and elevated titers of anti-MAG antibodies.
Externí odkaz:
https://doaj.org/article/cf5e6c5391df4520905f166f2df2ed5d
Autor:
Angelica C. Cornejo, Norman Latov
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28870- (2024)
Background: Anti-MAG neuropathy is a slowly progressive demyelinating neuropathy that can lead to disability. The neuropathy is thought to be caused by monoclonal IgM antibodies that target the Myelin Associated Glycoprotein (MAG) in peripheral nerve
Externí odkaz:
https://doaj.org/article/067354de00ac4651808fda3a20663dec
Autor:
Norman Latov
Publikováno v:
Microorganisms, Vol 11, Iss 3, p 640 (2023)
The authors wish to make the following corrections to this paper [...]
Externí odkaz:
https://doaj.org/article/f7efe42a8c414df0951f5343b4649f3a
Autor:
Norman Latov
Publikováno v:
Microorganisms, Vol 10, Iss 11, p 2139 (2022)
Preceding infection with Campylobacter jejuni (Cj) occurs in approximately 30% of patients with Guillain–Barre syndrome (GBS), and the risk of GBS following Cj infection is increased by 77 to 100-fold. GBS is most often of the axonal subtype and is
Externí odkaz:
https://doaj.org/article/650d97c2dda8455a8574d61ced924932
Autor:
Mims Cushing, Norman Latov, MD, PhD
Peripheral neuropathy is one of the most common diseases most people never heard of and yet, upwards of 20 million Americans have it! It is estimated that 60 to 70 percent of people with diabetes have mild to severe neuropathy. That fact alone is sta
Autor:
Norman Latov, MD, PhD
Peripheral neuropathy affects 10 to 20 million people in the U.S, including ten per cent of all people who have diabetes. This condition has numerous causes, but can be associated with diseases such as HIV, alcoholism, and lupus, and may result from
Publikováno v:
Expert Review of Neurotherapeutics. 22:953-962
Introduction: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an autoimmune peripheral nerve disorder that is characterized by subacute onset, progressive or relapsing weakness, and sensory deficits. Proven treatments include intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88134da9c18688f38385d58d8051fa59
https://doi.org/10.1080/14737175.2022.2169134
https://doi.org/10.1080/14737175.2022.2169134
Autor:
Norman Latov
Publikováno v:
Expert Review of Clinical Immunology. 17:1269-1281
Introduction Autoimmune neuropathies have diverse presentations and underlying immune mechanisms. Demonstration of efficacy of therapeutic agents that inhibit the complement cascade would confirm the role of complement activation. D A review of the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245b4294851553216abb7c99c2b8564a
https://doi.org/10.1080/1744666x.2021.2002147
https://doi.org/10.1080/1744666x.2021.2002147
Autor:
Norman Latov
Publikováno v:
Current Opinion in Neurology. 34:625-630
PURPOSE OF REVIEW The diagnosis of Myelin-Associated Glycoprotein (MAG) neuropathy is based on the presence of elevated titers of IgM anti-MAG antibodies, which are typically associated with IgM monoclonal gammopathy, and a slowly progressive, distal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29ba0f0cdea89bb8282d2bdf6700cc34
https://doi.org/10.1097/wco.0000000000000975
https://doi.org/10.1097/wco.0000000000000975
Autor:
Ashwin Malhotra, Norman Latov
Publikováno v:
Journal of Clinical Neuromuscular Disease. 21:225-229
Bickerstaff brainstem encephalitis, widely considered to be associated with Miller Fisher and Guillain-Barré syndromes, is a rare disease state defined by the triad of ophthalmoplegia, ataxia, and decreased consciousness. The presence of central ner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c02ca11cda1531fa82209079eec3eca2
https://doi.org/10.1097/cnd.0000000000000282
https://doi.org/10.1097/cnd.0000000000000282