Results 141 to 150 of about 1,587,143 (318)
Current pharmacological treatment of idiopathic inflammatory myopathies [PDF]
The idiopathic inflammatory myopathies are uncommon and heterogeneous disorders. Their classification is based on distinct clinicopathologic features.
Alves, SC, Fasano, S, Isenberg, DA
core +1 more source
New insights into applications of base editor in hereditary disorders
Abstract Hereditary disorders are a group of diseases caused by genetic mutations or chromosomal variations. Although the incidence of each genetic disorder is relatively low, patients affected by the disease generally experience a range of severe symptoms, including blindness, disability, and even premature death. In addition, the available treatments
Maoping Cai +8 more
wiley +1 more source
Rituximab in the treatment of inflammatory myopathies: a review [PDF]
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
POS0490 USEFULNESS OF MHC-II IMMUNO-STAINING ON MUSCLE BIOPSIES IN IDIOPATHIC INFLAMMATORY MYOPATHIES [PDF]
M Robert +8 more
openalex +1 more source
Objective To describe the methodology used to develop new classification criteria for adult and juvenile idiopathic inflammatory myopathies (IIMs) and their major subgroups. Methods An international, multidisciplinary group of myositis experts produced a
M. Bottai +37 more
semanticscholar +1 more source
Dermatomyositis Like Presentation of Anti‐HMGCR Immune Mediated Necrotising Myopathy
ABSTRACT Extramuscular manifestations of anti‐3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase (HMGCR) immune‐mediated necrotising myopathy (IMNM) are rare and often overlooked because they are overshadowed by predominant muscular symptoms. The types of cutaneous manifestations can be numerous.
Lionel Leblanc +4 more
wiley +1 more source
Polymyositis and dermatomyositis – challenges in diagnosis and management
Polymyositis (PM) and dermatomyositis (DM) are different disease subtypes of idiopathic inflammatory myopathies (IIMs). The main clinical features of PM and DM include progressive symmetric, predominantly proximal muscle weakness.
Shu-Han Yang +2 more
doaj +1 more source
Az anti-Jo-1-pozitív antiszintetáz szindróma jellegzetességei gondozott betegeink alapján [PDF]
Absztrakt Bevezetés: Az idiopathiás inflammatorikus myopathiák a proximális végtagizmok szimmetrikus gyengeségével jellemezhető szisztémás autoimmun betegségek.
Bodoki, Levente +5 more
core +1 more source
Muscle Ultrasound in Inflammatory Myopathies: A Critical Review
Muscle ultrasonography is an upcoming tool in the evaluation of neuromuscular disorders. It is easily applicable in multiple clinical settings, has no contraindications, and provides a cost-effective alternative to other imaging modalities such as MRI ...
Leeuwenberg Kristofoor E, Albayda Jemima
semanticscholar +1 more source
ABSTRACT Mitochondrial dysfunction and energy imbalance caused by chemotherapy are key contributors to skeletal muscle atrophy, which severely impacts the quality of life in cancer patients. Paclitaxel, a commonly used chemotherapeutic agent, is known to promote muscle wasting and cellular senescence, largely by impairing mitochondrial function.
Yu‐Fan Chuang +6 more
wiley +1 more source

