Results 31 to 40 of about 15,538 (160)

Basic requirements to establish a neuromuscular laboratory

Indian Journal of Pathology and Microbiology, 2022
Histopathological analysis of muscle biopsy is a prerequisite in the evaluation of neuromuscular disorders, particularly inflammatory myopathies, metabolic myopathies, congenital myopathies, muscular dystrophies and differentiating myopathies and ...
Bevinahalli N Nandeesh, Gayathri Narayanappa, T C Yasha   +2 more
doaj   +1 more source

Failure of daratumumab in the treatment of anti-synthetase syndrome: A case report

SAGE Open Medical Case Reports
Anti-synthetase syndrome is a subset of idiopathic inflammatory myopathies, for which refractory disease can be difficult to treat. Daratumumab, an anti-CD38 monoclonal antibody primarily used in hematologic malignancies, has recently shown promise in ...
Nam Nguyen, Valérie Leclair, Rayan Kaedbey, Marie Hudson   +3 more
doaj   +1 more source

Idiopathic inflammatory myopathies and the lung

European Respiratory Review, 2015
Idiopathic inflammatory myositis (IIM) is a group of rare connective tissue diseases (CTDs) characterised by muscular and extramuscular signs, in which lung involvement is a challenging issue.
Jean-Christophe Lega, Quitterie Reynaud, Alexandre Belot, Nicole Fabien, Isabelle Durieu, Vincent Cottin   +5 more
doaj   +1 more source

Imaging biomarkers in the idiopathic inflammatory myopathies

Frontiers in Neurology, 2023
Idiopathic inflammatory myopathies (IIMs) are a group of acquired muscle diseases with muscle inflammation, weakness, and other extra-muscular manifestations.
Adeel S. Zubair, Sharfaraz Salam, Mazen M. Dimachkie, Pedro M. Machado, Pedro M. Machado, Bhaskar Roy   +5 more
doaj   +1 more source

Ryanodine receptor type 1 content decrease‐induced endoplasmic reticulum stress is a hallmark of myopathies

Journal of Cachexia, Sarcopenia and Muscle, 2023
Background Decreased ryanodine receptor type 1 (RyR1) protein levels are a well‐described feature of recessive RYR1‐related myopathies. The aim of the present study was twofold: (1) to determine whether RyR1 content is also decreased in other myopathies ...
Jeremy Vidal, Eric A. Fernandez, Martin Wohlwend, Pirkka‐Pekka Laurila, Andrea Lopez‐Mejia, Julien Ochala, Alexander J. Lobrinus, Bengt Kayser, Isabel C. Lopez‐Mejia, Nicolas Place, Nadège Zanou   +10 more
doaj   +1 more source

Miopatías inflamatorias

Revista Médica Clínica Las Condes, 2018
RESUMEN: Las miopatías inflamatorias son un grupo heterogéneo de enfermedades adquiridas del músculo estriado esquelético que comparten la injuria muscular inmunomediada como característica común.
Jorge A. Bevilacqua, MD, PhD, Nicholas Earle, MD   +1 more
doaj   +1 more source

Antiangiogenic VEGF Isoform in Inflammatory Myopathies

Mediators of Inflammation, 2013
Objective. To investigate expression of vascular endothelial growth factor (VEGF) antiangiogenic isoform A-165b on human muscle in idiopathic inflammatory myopathies (IIM) and to compare distribution of angiogenic/antiangiogenic VEGFs, as isoforms shifts
Nila Volpi, Alessandra Pecorelli, Paola Lorenzoni, Francesco Di Lazzaro, Giuseppe Belmonte, Margherita Aglianò, Luca Cantarini, Fabio Giannini, Giovanni Grasso, Giuseppe Valacchi   +9 more
doaj   +1 more source

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

Acta Neuropathologica Communications
Inflammatory myopathies represent a heterogeneous group of autoimmune disorders affecting skeletal muscle, with distinct pathological features. While muscle biopsy remains a key diagnostic tool, conventional immunohistochemical approaches are limited in ...
Monica Sciacco, Daniele Velardo, Letizia Bertolasi, Patrizia Ciscato, Giuseppe Castellano, Deborah Mattinzoli, Masami Ikehata, Stefania Corti, Giacomo Pietro Comi, Simona Zanotti   +9 more
doaj   +1 more source

Top ten discoveries of the year: Neuromuscular disease

Free Neuropathology, 2020
This review highlights ten important advances in the neuromuscular disease field that either were first reported in 2019, or have reached a broad consensus during that year.
Marta Margeta
doaj   +1 more source

Sporadic inclusion body myositis in the rheumatology clinic

Indian Journal of Rheumatology, 2020
Sporadic inclusion body myositis (sIBM) is a progressive and insidious skeletal muscle disorder characterized classically by the quadriceps, wrist, and finger flexor weakness.
Fernando Henrique Carlos de Souza, Gustavo Luiz Behrens Pinto, Jean Marcos de Souza, Pablo Arturo Olivo Pallo, Leonardo Santos Hoff, Samuel Katsuyuki Shinjo   +5 more
doaj   +1 more source