Results 41 to 50 of about 1,337,423 (351)

Chronic tendon pathology: molecular basis and therapeutic implications [PDF]

, 2005
Tendons are frequently affected by chronic pain or rupture. Many causative factors have been implicated in the pathology, which until relatively recently was under-researched and poorly understood.
Riley, GP
core   +1 more source

Prevalence of Intracranial Aneurysms in Patients with Connective Tissue Diseases: A Retrospective Study

American Journal of Neuroradiology, 2016
BACKGROUND AND PURPOSE: Few studies have examined the prevalence of intracranial aneurysms in connective tissue diseases such as Marfan syndrome, Ehlers-Danlos syndrome, neurofibromatosis type 1, and Loeys-Dietz syndrome.
Sarasa Kim, W. Brinjikji, D. Kallmes
semanticscholar   +1 more source

Association study between immune-related miRNAs and mixed connective tissue disease

Arthritis Research & Therapy, 2021
Background Mixed connective tissue disease (MCTD) is a rare condition that is distinguished by the presence of specific U1-RNP antibodies. Information about its etiopathology and diagnostics is still unclear.
Barbara Stypińska, Aleksandra Lewandowska, Anna Felis-Giemza, Marzena Olesińska, Agnieszka Paradowska-Gorycka   +4 more
doaj   +1 more source

Usefulness in daily practice of the Systemic Lupus Erythematosus Disease Activity Index 2000 scale and the Systemic Lupus Erythematosus Disease Activity Score index for assessing the activity of systemic lupus erythematosus

Rheumatology
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by high hetero­geneity of clinical manifestations and an uncertain prognosis. Although the mortality rate due to SLE has decreased significantly in recent decades, there is still a
Dorota Suszek, Maciej Dubaj, Karol Bigosiński, Aleksandra Dembowska, Marcin Kaniewski, Wiktoria Sielwanowska, Bartosz Skierkowski, Izabela Dzikowska, Julia Sieczka, Maria Majdan   +9 more
doaj   +1 more source

Tetracycline Actions Relevant to Rosacea Treatment [PDF]

, 2009
Until today, the pathogenesis of rosacea is not known in detail. Yet in recent years evidence has been accumulating that rosacea with its common symptoms such as inflammatory lesions, erythema, telangiectasia, phymatous changes, and ocular symptoms is of
Korting, Hans Christian, Schöllmann, C.
core   +1 more source

Ultra‐rare sarcomas: A consensus paper from the Connective Tissue Oncology Society community of experts on the incidence threshold and the list of entities

Cancer, 2021
Among sarcomas, which are rare cancers, many types are exceedingly rare; however, a definition of ultra‐rare cancers has not been established. The problem of ultra‐rare sarcomas is particularly relevant because they represent unique diseases, and their ...
S. Stacchiotti, A. Frezza, J. Blay, E. Baldini, S. Bonvalot, J. Bovée, D. Callegaro, P. Casali, R. Chiang, G. Demetri, Elizabeth G. Demicco, J. Desai, M. Eriksson, H. Gelderblom, S. George, M. Gounder, A. Gronchi, Abha A. Gupta, R. Haas, Andrea Hayes-Jardon, P. Hohenberger, Kevin B. Jones, Robin L. Jones, B. Kasper, A. Kawai, D. Kirsch, E. Kleinerman, A. Le Cesne, Jiwon Lim, M. C. Chirlaque López, R. Maestro, R. Marcos-Gragera, Javier Martin Broto, T. Matsuda, O. Mir, Shreyaskumar R Patel, C. Raut, A. Razak, D. Reed, P. Rutkowski, R. Sanfilippo, M. Sbaraglia, I. Schaefer, D. Strauss, K. Sundby Hall, W. Tap, David M. Thomas, W. V. D. van der Graaf, W. V. van Houdt, O. Visser, M. von Mehren, A. Wagner, Breelyn A. Wilky, Y. Won, C. Fletcher, A. D. Dei Tos, A. Trama   +56 more
semanticscholar   +1 more source

Clinical Insights Into Hypercalcemia of Malignancy in Childhood

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Hypercalcemia of malignancy (HCM) is a rare but life‐threatening metabolic emergency in children that occurs in less than 1% of pediatric cancer cases, with a reported incidence ranging from 0.4% to 1.0% across different studies. While it is observed in 10%–20% of adult malignancies, pediatric HCM remains relatively uncommon.
Hüseyin Anıl Korkmaz
wiley   +1 more source

Eosinophilic granulomatosis with polyangiitis following flu guard influenza vaccination: A case report

Clinical Case Reports, 2023
Key Clinical Message This case highlights a potential association between influenza vaccination and the development of eosinophilic granulomatosis with polyangiitis (EGPA), prompting the need for increased vigilance regarding vaccine‐related autoimmune ...
Mehdi Jafarpour, Sara Daneshvar, Amir Taher Eftekharsadat, Alireza Khabbazi, Omid Pourbagherian   +4 more
doaj   +1 more source

Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome [PDF]

, 2015
Three international nosologies have been proposed for the diagnosis of Marfan syndrome (MFS): the Berlin nosology in 1988; the Ghent nosology in 1996 (Ghent-1); and the revised Ghent nosology in 2010 (Ghent-2).
Bannas, Peter, Behzadi, Cyrus, Bernhardt, Alexander M, Blankenberg, Stefan, De Backer, Julie, Fuisting, Bettina, Hillebrand, Mathias, Kölbel, Tilo, Püschel, Klaus, Robinson, Peter N, Rybczynski, Meike, Schüler, Helke, Sheikhzadeh, Sara, von Kodolitsch, Yskert   +13 more
core   +2 more sources

Mixed Connective Tissue Disease

Internal Medicine, 1999
Mixed connective tissue disease deserves to be a distinct disease entity due to the persistent citation of this disease in the literature since the original description by Sharp in 1972, in spite of the presence of several criticisms against the independency of this disease.
openaire   +3 more sources