Results 151 to 160 of about 2,269,213 (187)

High-plex spatial protein profiling of skeletal muscle biopsies in inflammatory myopathies using the MACSima™ imaging platform: A pilot study. [PDF]

open access: yesActa Neuropathol Commun
Sciacco M   +9 more
europepmc   +1 more source

ZCCHC4 Orchestrates Hepatocellular Carcinoma Metastasis by Regulating Lipid biosynthesis and TMEM97/LCN2/Twist1 Pathway. [PDF]

open access: yesInt J Biol Sci
Ye J   +14 more
europepmc   +1 more source

Anti-HMGCR and anti-DFS70 antibodies immunofluorescence patterns

Autoimmunity Reviews, 2017
We have replicated the findings of Alvarado-Cardenas et al. in our cohort of anti-HMGCR myositis patients, confirming the high specificity and sensibility of the rat liver IF pattern, especially when compared to the previously reported HEp-2 anti-HMGCR pattern.
Daniele Cammelli   +2 more
exaly   +3 more sources

Anti-HMGCR antibodies demonstrate high diagnostic value in the diagnosis of immune-mediated necrotizing myopathy following statin exposure

Immunologic Research, 2016
Anti-HMGCR antibodies represent a characteristic serological feature of statin-exposed and statin-unexposed patients with immune-mediated necrotizing myopathy (IMNM). We assessed anti-HMGCR antibodies in patients with suspected IMNM following statin exposure and patients with other autoimmune rheumatic diseases.
Miri Blank, M Mahler
exaly   +3 more sources

Cutaneous involvement in anti-HMGCR positive necrotizing myopathy [PDF]

open access: yesJournal of Autoimmunity, 2021
OBJECTIVE Anti-3-Hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) positive immune-mediated necrotizing myopathy (IMNM) is a rare disease. It is induced by exogenous substances, most often by statins. Little is known about cutaneous manifestations
Laurence Feldmeyer   +2 more
exaly   +3 more sources

Statin-induced immune-mediated necrotizing myopathy with concomitant increase of anti-HMGCR and anti-ACHR antibodies

Rheumatology International
Statin-induced immune-mediated necrotizing myopathy (IMNM) is a rare systemic neuromuscular condition. We present a case of a patient with a severe phenotype of the disease that was found to have an increase in anti-HMGCR and anti-ACHR antibodies. A potential association between these antibodies have not been previously described.
Sanjeev Herr, Razmig Garabet
exaly   +3 more sources

The prevalence and clinical characteristics of anti-HMGCR (anti-3-hydroxy-3-methyl-glutaryl-coenzyme A reductase) antibodies in idiopathic inflammatory myopathy: an analysis from the MyoCite registry

open access: yesRheumatology International, 2022
This study aimed to determine the prevalence and clinical characteristics of anti-HMGCR antibodies in idiopathic inflammatory myositis (IIM) at a tertiary care centre in northern India.
Ritu Verma, Arvind Nune, Vikas Agarwal
exaly   +2 more sources

CHARACTERISATION OF UK ANTI-HMGCR+ ANTIBODY ASSOCIATED MYOSITIS

Journal of Neurology, Neurosurgery & Psychiatry, 2016
Introduction Anti-HMG-CoA Reductase (anti-HMGCR) antibodies are associated with an immune-mediated necrotising myopathy related to previous ‘statin’ use. The role of this antibody in pathogenesis is incompletely understood. We have thoroughly characterised a cohort of anti-HMGCR associated myositis patients to increase understanding of the role of ...
Murphy, Sean   +8 more
openaire   +3 more sources

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