Results 71 to 80 of about 706,173 (166)
MedComm, Volume 6, Issue 12, December 2025.Protein arginine methyltransferase 1 (PRMT1) is a pivotal enzyme that catalyzes the asymmetric dimethylation of arginine residues, thereby functioning as a critical epigenetic regulator of diverse biological processes such as gene expression, RNA splicing, and DNA repair.
Yanqun Luo +4 more
wiley +1 more source
, 2011 Revised January 2011; application/pdf"This handbook was designed to provide information to parents, visitors and other interested individuals about the Kansas Juvenile Correctional Complex and its operation."Introduction General Programming ...
Kansas Juvenile Correctional Complex.
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Pediatric Dermatology, Volume 42, Issue 6, Page 1252-1254, November/December 2025.ABSTRACT Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by progressive heterotopic ossification (HO) and congenital malformation of the great toes. This case describes a 5‐year‐old Caucasian girl who initially presented with painless neck and back swelling as well as severe limitation of movement in the neck and ...
Orhan Yilmaz, Loretta Fiorillo
wiley +1 more source
Journal of Clinical and Translational Science, 2019 OBJECTIVES/SPECIFIC AIMS: To further explore the role of vWF in the pathogenesis of scleroderma by identifying its location within the tissue of sample biopsies obtained as part of routine diagnosis with the use of immuno-histochemical staining.
Natalia Vasquez Canizares +4 more
doaj +1 more source
Disabling pansclerotic morphea of childhood with extracutaneous manifestations
Indian Journal of Dermatology, 2013 Disabling pansclerotic morphea (DPM) of childhood is a rare generalized type of localized scleroderma (LS) that is known to follow an aggressive course with pansclerotic lesions leading to severe joint contractures and consequent immobility. Mortality is
Mahendra M Kura, Saurabh R Jindal
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Juvenile Localized Scleroderma: A Very Rare Case
Delta Medical College Journal, 2015 Juvenile localized scleroderma (JLS) is a rare chronic inflammatory and fibrosing disorder. It can result in significant morbidity, disfigurement, and severe functional, aesthetic and psychological disabilities. Patients with JLS should be identified early, evaluated extensively, treated aggressively, and monitored carefully.
Md Mahamudul Hasan +4 more
openaire +2 more sources
Revista Brasileira de ReumatologiaObjective: To assess esophageal involvement (EI) in juvenile localized scleroderma (JLS) population and the possible association between this gastrointestinal manifestation and demographic data, clinical features, laboratory exams, treatments and ...
Clarissa C.M. Valões +5 more
doaj +1 more source
Localized severe scleroderma: a retrospective study of 26 pediatric patients
, 2010 Juvenile localized scleroderma includes different conditions characterized by skin hardening with increased collagen deposition. Although juvenile localized scleroderma is considered a relatively benign disease, lesions may extend through the dermis ...
M. Beltramelli +9 more
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Esophagel involvement in juvenile localized scleroderma: A pilot study
, 2007 Objectives. To evaluate the esophageal involvement in patients with juvenile localized scleroderma (JLS). Methods. A cohort of patients with JLS underwent esophageal stationary manometry to evaluate esophageal motility and lower esophageal sphincter (LES)
Guariso G. +5 more
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, 2011 Juvenile scleroderma is a rare connective tissue disease that involves the skin and subcutaneous tissue. Among all presentations of juvenile scleroderma, localized scleroderma (JLSc) is the most frequent, followed by systemic disease (JSSc) and ...
Barbara Fiebig +4 more
core +1 more source