Classification and management of adult inflammatory myopathies

A Selva-O'Callaghan, I Pinal-Fernandez… - The Lancet …, 2018 - thelancet.com
Inflammatory myopathies, collectively known as myositis, are heterogeneous disorders
characterised by muscle inflammation, and frequently accompanied by extramuscular …

Statin-induced myalgia and myositis: an update on pathogenesis and clinical recommendations

A Selva-O'Callaghan… - Expert review of …, 2018 - Taylor & Francis
Introduction: Musculoskeletal manifestations are well-recognized side effects of treatment
with statins. New advances in this field have appeared in recent years. This review focuses …

Machine learning algorithms reveal unique gene expression profiles in muscle biopsies from patients with different types of myositis

I Pinal-Fernandez, M Casal-Dominguez… - Annals of the …, 2020 - ard.bmj.com
Objectives Myositis is a heterogeneous family of diseases that includes dermatomyositis
(DM), antisynthetase syndrome (AS), immune-mediated necrotising myopathy (IMNM) …

Tumour TIF1 mutations and loss of heterozygosity related to cancer-associated myositis

I Pinal-Fernandez, B Ferrer-Fabregas… - …, 2018 - academic.oup.com
Objectives To analyse the influence of genetic alterations and differential expression of
transcription intermediary factor 1 (TIF1) genes in the pathophysiology of cancer-associated …

Whole-body MRI and pathological findings in adult patients with myopathies

X Tomas, JC Milisenda, AI Garcia-Diez… - Skeletal Radiology, 2019 - Springer
Magnetic resonance imaging (MRI) is considered the most sensitive and specific imaging
technique for the detection of muscle diseases related to myopathies. Since 2008, the use of …

Transcriptomic profiling reveals distinct subsets of immune checkpoint inhibitor induced myositis

I Pinal-Fernandez, A Quintana, JC Milisenda… - Annals of the …, 2023 - ard.bmj.com
Objectives Inflammatory myopathy or myositis is a heterogeneous family of immune-
mediated diseases including dermatomyositis (DM), antisynthetase syndrome (AS), immune …

Mitochondrial DNA disturbances and deregulated expression of oxidative phosphorylation and mitochondrial fusion proteins in sporadic inclusion body myositis

M Catalán-García, G Garrabou, C Morén… - Clinical …, 2016 - portlandpress.com
Sporadic inclusion body myositis (sIBM) is one of the most common myopathies in elderly
people. Mitochondrial abnormalities at the histological level are present in these patients …

Coexisting autoantibodies against transcription factor Sp4 are associated with decreased cancer risk in patients with dermatomyositis with anti-TIF1γ autoantibodies

Y Hosono, B Sie, I Pinal-Fernandez, K Pak… - Annals of the …, 2023 - ard.bmj.com
Objectives In dermatomyositis (DM), autoantibodies are associated with unique clinical
phenotypes. For example, anti-TIF1γ autoantibodies are associated with an increased risk of …

[HTML][HTML] Exhaustion of mitochondrial and autophagic reserve may contribute to the development of LRRK2 G2019S -Parkinson's disease

DL Juárez-Flores, I González-Casacuberta… - Journal of translational …, 2018 - Springer
Background Mutations in leucine rich repeat kinase 2 (LRRK2) are the most common cause
of familial Parkinson's disease (PD). Mitochondrial and autophagic dysfunction has been …

[HTML][HTML] Identification of Unique microRNA Profiles in Different Types of Idiopathic Inflammatory Myopathy

S Muñoz-Braceras, I Pinal-Fernandez… - Cells, 2023 - mdpi.com
Dermatomyositis (DM), antisynthetase syndrome (AS), immune-mediated necrotizing
myopathy (IMNM), and inclusion body myositis (IBM) are four major types of idiopathic …