Results 101 to 110 of about 37,874 (304)

Otoneurological findings in an inflammatory myopathy case [PDF]

open access: yes, 2012
BACKGROUND: polymyositis is an idiopathic systematic disease characterized by a non-suppurative inflammatory process which attacks the skeletal musculature and manifests itself clinically by proximal and symmetrical muscular debility. It shows a variable
Klagenberg, Karlin Fabianne   +4 more
core   +1 more source

Successful Management of Presumed Reactivation of Neospora caninum Following Immunosuppression for Immune Thrombocytopenia in an Adult Doberman

open access: yesVeterinary Medicine and Science, Volume 11, Issue 4, July 2025.
Positive serology titres for Neospora caninum in the absence of appropriate clinical signs is not diagnostic for protozoal disease. Acute deterioration while immunosuppressed should raise concerns over reactivation of encysted protozoa, particularly in dogs with a history of raw feeding. Successful management of N. caninum appears possible but requires
Perrine Henry   +3 more
wiley   +1 more source

Dysferlinopathy: A Case Report and Literature Update

open access: yesİstanbul Medical Journal, 2016
Dysferlinopathy is a rare autosomal recessive myopathy, resulting in the lack or absence of dysferlin production caused by mutations in the encoding gene.
Orkide Kutlu   +7 more
doaj   +1 more source

Acute heart failure and rhabdomyolysis: a clue for the diagnosis of polymyositis with cardiac involvement

open access: yesReumatismo, 2017
Polymyositis is an idiopathic inflammatory myopathy, characterized by proximal muscle weakness and sometimes extramuscular manifestations. We report the case of a 51-year-old male, with history of complete heart block, which required pacemaker ...
P. Pinto-Lopes   +5 more
doaj   +1 more source

Rituximab in the treatment of inflammatory myopathies: a review [PDF]

open access: yes, 2017
Several uncontrolled studies have encouraged the use of rituximab (RTX) in patients with myositis. Unfortunately, the first placebo-phase trial to assess the efficacy of RTX in refractory myositis did not show a significant difference between the two ...
Fasano, S   +4 more
core  

First Phosphonic‐Type Inhibitors and Activity‐Based Probes Specific to the O'nyong‐nyong Virus Capsid Protease

open access: yesChemMedChem, Volume 20, Issue 12, June 17, 2025.
The serine capsid protease (CP) catalyzes a crucial process of the alphaviral replication cycle; therefore, it constitutes an interesting therapy target. Herein, the O'nyong‐nyong virus CP profile activity with a specific fluorogenic substrate is analyzed and examines the inhibitory activity of a new series of phosphonic analogs of tryptophan and ...
Karolina Torzyk‐Jurowska   +5 more
wiley   +1 more source

Ultrastructural muscle and neuro-muscular junction alterations in polymyositis

open access: yesНервно-мышечные болезни, 2015
Ultrastructural analysis of 7 biopsies from m.palmaris longus and m.deltoideus in patients with confirmed polymyositis revealed alterationand degeneration of muscle fibers and anomalies of neuro-muscular junction (NMJ).
L. L. Babakova, O. M. Pozdnyakov
doaj   +1 more source

Manual muscle testing and hand-held dynamometry in people with inflammatory myopathy : an intra- and interrater reliability and validity study [PDF]

open access: yes, 2018
Manual muscle testing (MMT) and hand-held dynamometry (HHD) are commonly used in people with inflammatory myopathy (IM), but their clinimetric properties have not yet been sufficiently studied.
Baschung Pfister, Pierrette   +5 more
core   +1 more source

Successful resection of liver metastasis detected by exacerbation of skin symptom in a patient with dermatomyositis accompanied by rectal cancer: a case report and literature review [PDF]

open access: yes, 2017
Background Dermatomyositis (DM) is a rare syndrome that belongs to the group of idiopathic inflammatory myopathies. The association between DM and malignancy is well recognized, and the severity of DM symptoms has been linked to the ...
Atsushi Kagimoto   +11 more
core   +1 more source

Juvenile dermatomyositis (JDM) and severe pulmonary involvement: case report [PDF]

open access: yes, 2009
Juvenile dermatomyositis (JDM) is an inflammatory, non-pustular disorder of skeletal muscles and skin. Other organs, such as the lungs, can be involved.
Bugni, Vanessa Monteiro   +5 more
core   +2 more sources

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