Results 51 to 60 of about 10,033 (195)

PReS-FINAL-2128: Quality of life and psychosocial aspects in juvenile localized scleroderma (JLS): a cross-sectional study in 40 patients [PDF]

Pediatr Rheumatol Online J, 2013
Culpo R, Ricca M, Vittadello F, Sequi G, Zulian F, Martini G.   +5 more
europepmc   +3 more sources

Developing juvenile localized scleroderma (jLS) consensus treatment regimens for comparative effectiveness studies [PDF]

Pediatric Rheumatology Online Journal, 2012
Li Suzanne C, Fuhlbrigge Robert C, Dedeoglu Fatma, Ferguson Polly J, Higgins Gloria C, Hong Sandy D, Jacobe Heidi, Lasky Andrew, Laxer Ronald M, Morris Mimi C, Pope Elena, Rabinovich C, Torok Kathryn S   +12 more
doaj   +2 more sources

DNA methylation patterns in juvenile systemic sclerosis and localized scleroderma

Clinical Immunology, 2021
Scleroderma refers to a group of chronic fibrotic immune-mediated diseases of unknown etiology. Characterizing epigenetic changes in childhood-onset scleroderma, systemic sclerosis or localized scleroderma, has not been previously performed. The aim of this study was to assess DNA methylation differences and similarities between juvenile systemic ...
Patrick Coit, Kaila L. Schollaert, Emily Mirizio, Kathryn S. Torok, Amr H. Sawalha   +4 more
openalex   +4 more sources

Neurological and psychological aspects of scleroderma of the face and neck in children

Лечащий Врач, 2021
In the structure of morbidity, among rheumatic diseases in children, juvenile scleroderma takes the third place in frequency after juvenile idiopathic arthritis and systemic lupus erythematosus.
M. S. Pavlova, L. G. Khachatryan, M. K. Osminina, N. A. Geppe, N. S. Podchernyaeva, V. M. Trepilets, M. D. Bogdanova, E. V. Kasanave, E. N. Tjurina, M. D. Velikoretskaya   +9 more
doaj   +1 more source

SHARE – workpackage 5: evidence based recommendations for diagnosis and treatment of juvenile localized scleroderma and juvenile systemic sclerosis [PDF]

Pediatr Rheumatol Online J, 2014
Culpo R, Vastert S, Ravelli A, Wulffraat N, Foeldvari I, Zulian F, Anton J, Avcin T, Baildam E, Boros C, Chaitow J, Constantin T, Dolezalova P, Kasapcopur O, de Oliveira S, Pilkington C, van Royen A, Russo R, Saad-Magalhaes C, Toplak N.   +19 more
europepmc   +3 more sources

Localized scleroderma in children

Przegląd Dermatologiczny, 2020
Localized scleroderma is an autoimmune disease affecting the dermis and underlying tissues (subcutaneous tissue, fascia, muscles, bones). The disease mainly occurs in women aged 20–50 years; however, children aged 7–10 years represent about 15% of all ...
Katarzyna A. Wolska-Gawron, Dorota Krasowska   +1 more
doaj   +1 more source

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.
Nibedita Paul, Md Rafiqul Islam, Nadia Nusrat, Lazina Sharmin, Md Mahamudul Hasan   +4 more
openalex   +3 more sources

Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis [PDF]

, 2014
In this study, 1,833 systemic sclerosis (SSc) cases and 3,466 controls were genotyped with the Immunochip array. Classical alleles, amino acid residues, and SNPs across the human leukocyte antigen (HLA) region were imputed and tested.
, Airó, Paolo, Alarcón-Riquelme, Marta, AlKassab, Firas, Arnett, Frank C., Assassi, Shervin, Baron, Murray, Beretta, Lorenzo, Bossini-Castillo, Lara, Broen, Jasper, Brown, Matthew, Carmona, Francisco David, Carreira, Patricia, Castellví, Iván, Chen, Wei V., Denton, Christopher, Distler, Jörg H.W., Docherty, Peter, Fessler, Barri J., Fonseca, Carmen, Frech, Tracy M., Furst, Daniel E., González-Gay, Miguel Ángel, Gorlova, Olga, Gregersen, Peter K., Guerra, Sandra, Herrick, Ariane, Hesselstrand, Roger, Hinchcliff, Monique E., Hudson, Marie, Hummers, Laura K., Hunzelmann, Nicolas, Jones, Henry Niall, Kaminska, Elzbieta, Khalidi, Nader, Khanna, Dinesh, Koeleman, Bobby P., Kreuter, Alexander, Lafyatis, Robert A., Lee, Annette T., Lunardi, Claudio, López-Isac, Elena, Markland, Janet, Martin, Javier, Martin, José Ezequiel, Mayes, Maureen D., Molitor, Jerry A., Nordin, Annika, Ochoa, Eguzkine, Padyukov, Leonid, Phillips, Kristin, Pope, Janet E., Radstake, Timothy R.D.J., Reveille, John D., Riemekasten, Gabriela, Robinson, David, Schiopu, Elena, Schuerwegh, Annemie J., Segal, Barbara M., Shiels, Paul, Silver, Richard M., Simeón, Carmen Pilar, Simms, Robert W., Steen, Virginia D., Tan, Filemon K., Teruel, María, van Laar, Jacob M., Varga, John, Voskuyl, Alexandre E., Wigley, Fredrick M., Wijmenga, Cisca, Witte, Torsten, Worthington, Jane, Ying, Jun, Zhernakova, Alexandra, Zhou, Xiaodong   +75 more
core   +1 more source

Recent Advances in Systemic Scleroderma in Childhood [PDF]

, 2015
Ann Paediatr Rheumatol Annals of paediatric rheumatolog http://www.aprjournal.org/ 2146-2909 ...
Constantin, Tamás, Györgyi, Zoltán, Ivan Foeldvari, Peter Weiser, Szabó, András   +4 more
core   +1 more source

Pansclerotic Morphea with Features of Eosinophilic Fasciitis: Distinct Entities or Part of a Continuum? [PDF]

, 2014
Scleroderma is a highly complex disorder in its clinical manifestations and pathogenesis. It has a wide range of clinical manifestations due to varying degrees of vasculopathy, autoimmunity, altered endothelium function, and abnormal fibrosis.
Canty, Kristi, Hoeltzel, Mark F., Odhav, Ashika   +2 more
core   +1 more source