Results 31 to 40 of about 1,856,619 (235)

Assessment of tissue fibrosis in skin biopsies from patients with systemic sclerosis employing confocal laser scanning microscopy: an objective outcome measure for clinical trials? [PDF]

, 2010
OBJECTIVES: To obtain an objective, unbiased assessment of skin fibrosis in patients with SSc for use in clinical trials of SSc disease-modifying therapeutics.
Busquets, Joanna, Del Galdo, Francesco, Jimenez, Sergio A., Kissin, Eugene Y.   +3 more
core   +3 more sources

Scleroderma with Nodular Scleroderma

Case Reports in Dermatology, 2016
Background: Nodular scleroderma is a rare variant of scleroderma which can occur in connection with systemic sclerosis or morphea. A biopsy from the lesion can demonstrate the scleroderma pattern, i.e., keloid pattern or mixed type.
Chutika Srisuttiyakorn, Kobkul Aunhachoke   +1 more
doaj   +1 more source

Cerebral infarction caused by systemic sclerosis: a case report

Journal of International Medical Research, 2021
Systemic sclerosis, also known as scleroderma, is a rare multisystem autoimmune disease characterized by vascular lesions caused by collagen deposition in the skin and viscera and damage to the endothelium.
Qingqing Wang, Mengen Zhang, Mingfeng Zhai, Zongyou Li   +3 more
doaj   +1 more source

Calcinosis circumscripta of the breasts: The deeper meaning

South African Journal of Radiology, 2023
Calcinosis circumscripta involving the breasts usually hints at an underlying systemic cause, most commonly connective tissue disorders such as scleroderma or dermatomyositis.
Tanusha Sewchuran, Joel M. Kabeya
doaj   +1 more source

A prospective observational study of mycophenolate mofetil treatment in progressive diffuse cutaneous systemic sclerosis of recent onset. [PDF]

, 2012
OBJECTIVE: A prospective observational study of mycophenolate mofetil (MMF) treatment in patients with diffuse progressive cutaneous systemic sclerosis (SSc) of recent onset.
Jimenez, Sergio A., Lee, MD, Jason B., Mendoza, MD, Fabian A., Nagle, Sarah J.   +3 more
core   +3 more sources

Improvement of mouth functional disability in systemic sclerosis patients over one year in a trial of fat transplantation versus adipose-derived stromal cells [PDF]

, 2016
Background. Systemic sclerosis (SSc) is a multisystem disease characterized by cutaneous and visceral fibrosis. Face and mouth changes include telangiectasia, sicca syndrome, and thinning and reduction of mouth width (microcheilia) and opening ...
CARELLA, SARA, FINO, PASQUALE, FIORAMONTI, Paolo, MARCHESE, Cinzia, ONESTI, Maria Giuseppina, SCUDERI, Nicolo'   +5 more
core   +4 more sources

Systemic Sclerosis Manifesting Post-Radiotherapy: A Case Report

European Medical Journal Dermatology, 2023
Morphoea is a chronic inflammatory disease of the skin and underlying tissues, characterised by fibrosis of the skin and subcutaneous tissue without systemic involvement.
Devanshi Nimbark, Hita H. Mehta, Manal D. Dave   +2 more
doaj   +1 more source

Phenotypes Determined by Cluster Analysis and Their Survival in the Prospective European Scleroderma Trials and Research Cohort of Patients With Systemic Sclerosis

Arthritis & Rheumatology, 2019
Systemic sclerosis (SSc) is a heterogeneous connective tissue disease that is typically subdivided into limited cutaneous SSc (lcSSc) and diffuse cutaneous SSc (dcSSc) depending on the extent of skin involvement.
V. Sobanski, J. Giovannelli, Y. Allanore, G. Riemekasten, P. Airò, S. Vettori, F. Cozzi, O. Distler, M. Matucci-Cerinic, C. Denton, D. Launay, E. Hachulla, S. Guiducci, U. Walker, D. Kyburz, G. Lapadula, F. Iannone, B. Maurer, S. Jordan, R. Bečvář, Stanislaw Sierakowsky, Otylia Kowal Bielecka, M. Cutolo, A. Sulli, G. Valentini, G. Cuomo, E. Siegert, S. Rednic, I. Nicoara, A. Kahan, P. Vlachoyiannopoulos, C. Montecucco, R. Caporali, J. Štork, M. Inanç, P. Carreira, S. Novak, L. Czirják, C. Varjú, C. Chizzolini, E. Kucharz, A. Kotulska, M. Kopeć-Mędrek, M. Widuchowska, B. Rozman, C. Mallia, B. Coleiro, A. Gabrielli, D. Farge, Chen Wu, Z. Marjanovic, Helene Faivre, Darin Hij, Roza Dhamadi, P. Airò, R. Hesselstrand, F. Wollheim, D. Wuttge, K. Andréasson, D. Martinović, A. Balbir-Gurman, Y. Braun-Moscovici, F. Trotta, A. Lo Monaco, N. Hunzelmann, R. Pellerito, Ospedale Mauriziano, Lisa Maria Bambara, P. Caramaschi, J. Morović-Vergles, C. Black, N. Damjanov, J. Henes, Vera Ortiz Santamaria, S. Heitmann, D. Krasowska, M. Seidel, P. Hasler, H. Burkhardt, A. Himsel, G. Bajocchi, Arcispedale Santa Maria Nuova, M. João Salvador, J. A. Pereira da Silva, B. Stamenkovic, A. Stanković, Carlo Francesco Selmi, M. De Santis, B. Marasini, M. Tikly, L. Ananieva, L. Denisov, U. Müller-Ladner, M. Frerix, I. Tarner, R. Scorza, F. Puppo, M. Engelhart, G. Strauss, H. Nielsen, K. Damgaard, G. Szücs, S. Szamosi, A. Z. Zea Mendoza, C. Puente, W. S. Sifuentes Giraldo, Ø. Midtvedt, S. Reiseter, T. Garen, G. Valesini, V. Riccieri, Ruxandra Maria Ionescu, D. Opris, L. Groșeanu, F. Wigley, Roxana Sfrent Cornateanu, R. Ioniţescu, Ana Maria Gherghe, A. Soare, M. Gorga, M. Bojincă, C. Mihai, M. Milicescu, C. Sunderkötter, Annegret Kuhn, N. Sandorfi, G. Schett, J. Distler, C. Beyer, P. Meroni, F. Ingegnoli, L. Mouthon, F. de Keyser, V. Smith, Francesco Paolo Cantatore, A. Corrado, S. Ullman, L. Iversen, Carlos Alberto von Mühlen, Jussara Marilu Bohn, Lilian Scussel Lonzetti, Maria Rosa Pozzi, K. Eyerich, R. Hein, E. Knott, P. Wiland, M. Szmyrka-Kaczmarek, R. Sokolik, E. Morgiel, M. Madej, F. Houssiau, Juan Jose Alegre‐Sancho, B. Krummel-Lorenz, P. Saar, M. Aringer, C. Günther, R. Westhovens, E. Langhe, J. Lenaerts, B. Anić, M. Barešić, M. Mayer, Maria Üprus, K. Otsa, Ş. Yavuz, B. Granel, Sebastião Cezar Radominski, Carolina Souza Müller, V. Azevedo, S. Jimenez, Joanna Busquets, S. Agachi, L. Groppa, Lealea Chiaburu, E. Russu, S. Popa, T. Zénone, M. Pileckytė, S. Stebbings, J. Highton, A. Mathieu, A. Vacca, P. Sampaio-Barros, N. Yoshinari, R. Marangoni, P. Martin, Luiza Fuocco, L. Stamp, P. Chapman, J. O’Donnell, K. Solanki, A. Doube, D. Veale, M. O’Rourke, E. Loyo, Mengtao Li, Walid Ahmed Abdel Atty Mohamed, E. Rosato, A. Amoroso, A. Gigante, F. Oksel, F. Yargucu, C. Tanaseanu, Monica Popescu, A. Dumitrașcu, I. Tiglea, R. Foti, R. Chirieac, C. Ancuta, D. Furst, P. Villiger, S. Adler, J. Laar, C. Kayser, Andrade Luis Eduardo C., N. Fathi, M. Hassanien, Paloma García Peña Lefebvre, S. Rodríguez Rubio, Marta Valero Expósito, J. Sibilia, E. Chatelus, J. Gottenberg, Hélène Chifflot, I. Litinsky, P. Emery, M. Buch, F. del Galdo, A. Venalis, I. Butrimienė, P. Venalis, R. Rugiene, D. Karpec, Lesley Ann Saketkoo, J. Lasky, E. Kerzberg, Fabiana Montoya, V. Cosentino, M. Limonta, Antonio Luca Brucato, E. Lupi, I. Rosner, M. Rozenbaum, G. Slobodin, N. Boulman, D. Rimar, M. Couto, F. Spertini, C. Ribi, G. Buss, S. Kahl, V. Hsu, Fei Chen, D. McCloskey, Halina Malveaux, Jean Louis Pasquali, T. Martin, A. Gorse, A. Guffroy, V. Poindron   +259 more
semanticscholar   +1 more source

Cerebral Sinus Thrombosis in Scleroderma: A Case Report [PDF]

Acta Medica Iranica, 2012
Scleroderma or systemic sclerosis is a multisystem disease due to excessive collagen deposition in different organs and autoimmunity by production of autoantibodies.According to previous reports, brain is rarely affected in scleroderma, howeverrecent ...
Maryam Poursadegh Fard, Sina Karami Magham   +1 more
doaj   +2 more sources

THE SYSTEMIC INVOLVEMENT IN SCLERODERMA [PDF]

Medical Journal of Australia, 1977
A survey was made of the systemic involvement in 38 patients with scleroderma: 33 with the acrosclerotic form (Type 1, 18, Type 2, 15) and five with the diffuse form. The study comprised inquiry about symptoms, physical examination, and the laboratory tests, such as radiological examination of chest and hands, barium swallow and meal X-ray examination,
openaire   +2 more sources