A.‐R. Moslemi

A Local Antigen-Driven Humoral Response Is Present in the Inflammatory Myopathies

Sporadic inclusion body myositis—diagnosis, pathogenesis and therapeutic strategies

Inclusion body myositis and myopathies

Estrogen receptors and human disease

Paraneoplastic Syndromes Involving the Nervous System

Upregulated inducible co-stimulator (ICOS) and ICOS-ligand in inclusion body myositis muscle: significance for CD8+ T cell cytotoxicity

Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy

Emerging roles of tRNA in adaptive translation, signalling dynamics and disease

Inflammatory myopathies: Clinical, diagnostic and therapeutic aspects

Are mitochondria critical in the pathogenesis of Alzheimer's disease?

Dynamic RNA Modifications in Gene Expression Regulation

Inclusion body myositis with human immunodeficiency virus infection: Four cases with clonal expansion of viral‐specific T cells

Alzheimer's disease

Liquid chromatography-tandem mass spectrometry-based fragmentation analysis of glycopeptides

A Pragmatic Guide to Enrichment Strategies for Mass Spectrometry–Based Glycoproteomics

Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis

Oxidative stress and neurodegeneration: where are we now?

Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches

Inflammatory Muscle Diseases

Oxidative stress, mitochondrial damage and neurodegenerative diseases.

Estrogen Receptor Mutations in Human Disease

Chemical Glycoproteomics

Inclusion-body myositis

Leigh Syndrome with Cytochrome-c Oxidase Deficiency and a Single T Insertion nt 5537 in the Mitochondrial tRNA^TrpGene

Inclusion Body Myositis: Clonal Expansions of Muscle‐Infiltrating T Cells Persist Over Time

Limited T‐Cell Receptor V Gene Usage in Inclusion Body Myositis

P4.46 Molecular pathogenesis of a new glycogenosis caused by a mutation in glycogenin-1

Estrogen receptor alpha in giant cell arteritis: a molecular genetic study.

Mitochondrial abnormalities in inclusion-body myositis