Results 91 to 100 of about 3,722 (185)

Epidemiological analysis of patients with Dupuytren's disease

Revista Brasileira de Ortopedia
Objective: To evaluate the risk factors and analyze the characteristics of patients and lesions in Dupuytren's disease. Methods: Retrospective analysis of patients diagnosed with Dupuytren's disease in a hand surgery clinic in 2013.
Henrique Gonçalves Mansur, Edmo Rodrigues de Oliveira, Cesar Barbosa Gonçalves   +2 more
doaj   +1 more source

Reduced telomere length is associated with fibrotic joint disease suggesting that impaired telomere repair contributes to joint fibrosis [PDF]

, 2018
OBJECTIVE: Joint fibrosis affects many synovial joints (including hip, knee and shoulder) causing stiffness and pain. The mechanism of joint fibrosis remains unknown, although genetic factors may contribute.
Borthwick, LA, Brock, TM, Deehan, DJ, Fabiane, SM, Kalson, NS, Mangino, M, Mann, DA, Williams, FMK   +7 more
core  

The importance of multiple Z- plasty- assisted physical therapy in the treatment of Dupuytren’s contracture

Journal of Orthopaedic Surgery and Research
Background The palmar aponeurosis is extremely adherent to the skin above it. Many of the pre-tendinous coarse fibers enter the dermis at an angle, not just in the palmar creases but also throughout the palm.
Nader Gomaa Elmelegy, Dalia Nader
doaj   +1 more source

Dupuytren’s Contracture in Athletes

Quality in Sport
Background. Dupuytren’s contracture is a fibrotic condition of the hand, traditionally associated with age, genetics, and metabolic factors. However, recent observations suggest it may also appear in younger individuals with high physical activity ...
Tomasz Antczak, Monika Gajda-Bathelt , Monika Dąbek, Katarzyna Jania, Zuzanna Perlicka , Karolina Smolińska , Paulina Sadkowska , Julia Kulczycka , Weronika Popow , Michał Ciołkosz   +9 more
doaj   +1 more source

Reduced WNT4 expression in normal skin fibroblasts leads to ‘Dupuytren-like’ changes in the transcriptome

Heliyon
Background: Dupuytren's disease (DD) is a fibro-proliferative disorder of unknown aetiology. Previous studies have implicated multiple WNT signalling genes/proteins in Dupuytren pathology, including WNT4.
Aoife O'Brien, Andrew Stevenson, Lucy Barrett, Nicholas B. Lawler, Nicole Hortin, Zhenjun Deng, Amira Allahham, Fabio Quondamatteo, Nicole Smith, K. Swaminathan Iyer, Fiona M. Wood, Mark W. Fear   +11 more
doaj   +1 more source

ISEV2025 Abstract Book

Journal of Extracellular Vesicles, Volume 14, Issue S1, October 2025.
wiley   +1 more source

UEG Week 2025 Moderated Posters

United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley   +1 more source

Dupuytren’s Disease

, 2018
Raoul Tubiana, Caroline Leclercq, Lawrence C. Hurst, Marie A. Badalamente, and Evelyn J. Mackin. With contributions by Jean-Jacques Comtet and Terri M. Skirven and illustrations by Leon Dorn. London: Martin Dunitz; 2000. 336 pages. $125.00. Dupuytren disease has been a challenge to surgeons since Dupuytren first described it in 1832.
Johnson, Jeremiah D., Pavano, Colin, Rodner, Craig   +2 more
openaire   +3 more sources

Dupuytren's Disease: Anatomy and Surgical Treatment [PDF]

, 1988
The principal aim of this written account is to describe the evolution of a surgical approach to the treatment of Dupuytren's Disease based on current knowledge of pathogenesis and precise description of the anatomy. The historical record of the life and
McGrouther, Duncan Angus
core  

Newer application of Oncothermia to non-malignant diseases such as Dupuytren's contracture of the hand and chronic lower back pain lasting more than 4 weeks [PDF]

, 2017
Hegyi, Gabriella, Molnár, István, Máté, Ágnes, Szőke, Henrik   +3 more
core   +1 more source