Results 191 to 200 of about 15,772 (257)

Presurgical miR‐675‐5p Associates With the Inflammatory Response Following Surgery and Increases Inflammatory Gene Expression In Vitro

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 4, August 2026.
ABSTRACT Background A loss of muscle mass and strength is a marker of poor outcomes following surgery. Changes in muscle gene expression following surgery are likely to contribute to postsurgical muscle loss, but the mechanisms controlling these changes are not known. We have previously shown that miRNAs associate with muscle loss in disease, including
Narmin Akhundova, Richard Paul, Benjamin Fletcher, Martin Connolly, Mark J. Griffiths, Paul R. Kemp   +5 more
wiley   +1 more source

CN-macroEMG does not provide additional support for diagnosing inflammatory myopathies. [PDF]

Eur J Transl Myol
Finsterer J.
europepmc   +1 more source

Repercussions of Diagnostic Delay in Rare Diseases

Journal of Genetic Counseling, Volume 35, Issue 4, August 2026.
ABSTRACT Rare diseases (RDs) are often subject to diagnostic delays due to their low prevalence, clinical variability, and limited professional awareness. This scoping review aimed to map the literature on these delays, examining their clinical, emotional, and socioeconomic consequences.
Luisa Rezende Batista, Luiza Fernandes Valente, Fernando Spina, Davi Said Gonçalves Celso, Israel Gomy, Christiane Mariotini‐Moura   +5 more
wiley   +1 more source

Myxovirus Resistance A Protein Expression in Idiopathic Inflammatory Myopathies and Hereditary Muscle Diseases with Inflammatory Cell Infiltration: A North African Study. [PDF]

Int J Mol Sci
Farhat E, Zamali I, Younes TB, Klaa H, Stenzel W, Samoud S, Ben Rhouma H, Galai Y, Ben Youssef-Turki I, Kraoua I, Ben Ahmed M, Ben Hmid A.   +11 more
europepmc   +1 more source

Psychosocial Determinants of Pain in Muscle Biopsy

Muscle &Nerve, Volume 74, Issue 2, Page 383-389, August 2026.
ABSTRACT Introduction/Aims Open muscle biopsy (OMB) is a key diagnostic tool for neuromuscular diseases, though patients often worry about risks and discomfort. This study aimed to assess pain during and after OMB, factors influencing pain perception, and adverse events.
Beatrice Labella, Emmanuelle Lacene, Maud Beuvin, Anaïs Chanut, Angeline Madelaine, Favienne Levy‐Borsato, Guy Brochier, Clémence Labasse, Guillaume Bassez, Danielle Seilhean, Sarah Leonard‐Louis, Teresinha Evangelista   +11 more
wiley   +1 more source

Identification of Novel Risk Loci for Common B-Cell Lymphoma Subtypes Through Cross-Trait Analysis with Idiopathic Inflammatory Myopathies. [PDF]

Cancers (Basel)
Che WI, Jarvis JN, International Lymphoma Epidemiology Consortium InterLymph, Imacs Genetics Group Myogen, Lundberg IE, Smedby KE, Lamb JA, Holmqvist M.   +7 more
europepmc   +1 more source

Quantitative Guanidinium CEST‐Based pH Mapping at 3 T in Healthy and Pathological Muscle

NMR in Biomedicine, Volume 39, Issue 8, August 2026.
Chemical exchange saturation transfer (CEST) enables high‐resolution pH mapping by measuring the exchange rate between guanidinium and water protons. The current method is based on the Z‐spectra fitting with Bloch–McConnell (BM) equations and allows us to detect pH variations on the order of 0.02 pH units in the very restrained pathophysiological pH ...
Valentin Henriet, Pierre‐Yves Baudin, Benjamin Marty, Marc Lapert, Harmen Reyngoudt   +4 more
wiley   +1 more source

Idiopathic inflammatory myopathies: new therapeutic horizons [PDF]

ARP Rheumatology
Raquel Campanilho Marques
doaj  

HLA loci heterozygosity modulates genetic risk in idiopathic inflammatory myopathies. [PDF]

Ann Rheum Dis
Chen G, Zhu C, Chinoy H, Amos CI, Morris AP, Lamb JA, International Myositis Assessment & Clinical Studies Group (IMACS) Myositis Genetics Scientific Interest Group (MYOGEN).   +6 more
europepmc   +1 more source

Review of nutrition management of pediatric intestinal pseudo‐obstruction

Nutrition in Clinical Practice, Volume 41, Issue 4, Page 1048-1060, August 2026.
Abstract Chronic intestinal pseudo‐obstruction (CIPO) is a rare, heterogeneous, and debilitating disorder characterized by profound intestinal dysmotility and severe nutrition challenges. Its presentation resembles that of mechanical bowel obstruction, but CIPO occurs in the absence of luminal obstruction.
Senthilkumar Sankararaman, Raisa Rani James, Bushra El‐Amaireh, Andrea Adler, Kadakkal Radhakrishnan, Sujithra Velayuthan   +5 more
wiley   +1 more source