Results 41 to 50 of about 2,725,905 (151)
Journal of Cellular and Molecular Medicine, Volume 30, Issue 18, September 2026.ABSTRACT Cartilage fibrosis contributes to extracellular matrix remodelling and structural deterioration during osteoarthritis (OA) progression; however, the molecular regulators involved in this process remain incompletely understood. Stanniocalcin‐1 (STC1) has been implicated in tissue remodelling and fibrosis‐associated signalling, but its role in ...
Guang Zhu +9 more
wiley +1 more source
Secondary hypertrophic osteoarthropathy in a patient with pulmonary carcinoma
Bratislava Medical Journal, 2000 Hypertrophic osteoarthropathy (HOA) is a syndrome that manifests itself by clubbing of fingers, periosteal and osteal neoformation in acral bones and oligo- or polysynovitis. It may occur as primary form (mostly hereditary) or secondary form, associated with various diseases, especially neoplastic or infectious diseases.The purpose of the study was to ...
H, Raffayova, P, Schultz, F, Malis
openaire +2 more sources
Pachydermoperiostosis-Like Disease In Captive Red Ruffled Lemurs (Varecia Variegatus Rubra) [PDF]
, 2011 Pachydermatoperiostosis, a rare form of hypertrophic osteoarthropathy, is of unknown etiology and previously thought limited to humans. The only periosteal reaction previously reported in prosimians is related to renal disease.
Bruce Rothschild +2 more
core
Hypertrophic osteoarthropathy in a child with chronic liver disease [PDF]
, 2014 Hypertrophic osteoarthropathy (HOA) is an uncommon condition in children, consisting of a triad of digital clubbing, non-inflammatory joint effusions and radiographic evidence of periostitis affecting the hands, feet and distal long bones.
Wittenberg, Dankwart F. +2 more
core +1 more source
Geriatrics &Gerontology International, Volume 26, Issue 2, February 2026.The main features of late‐onset rheumatoid arthritis (LORA), manifesting after age 65, are acute onset, higher disease activity, systemic involvement, and less presence of autoantibodies. Management requires individualized strategies, balancing aggressive treat‐to‐target therapy in robust patients with frailty‐focused approaches to prevent geriatric ...
Fausto Salaffi +6 more
wiley +1 more source
Hypertrophic Osteopathy Associated With Intrathoracic Masses in 5 Dogs and Review of the Literature
Veterinary Medicine International, Volume 2026, Issue 1, 2026.This study describes the clinical and radiographical findings of hypertrophic osteopathy in 5 female mature adult dogs with pulmonary and mediastinal masses. Besides, the literature review from the past to today provides information about the disease.
Mehmet Alper Cetinkaya +5 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2004 Os autores descrevem caso de baqueteamento digital, o qual possibilitou diagnóstico de carcinoma broncogênico em paciente assintomático. Baseados em levantamento bibliográfico, discutem sua fisiopatologia, associações com alterações sistêmicas e métodos ...
Alex Gonçalves Macedo +4 more
doaj +1 more source
Beyond Cystic Fibrosis: Recognising Shwachman‐Diamond Syndrome in the Respiratory Clinic
Respirology Case Reports, Volume 13, Issue 12, December 2025.Our case shows how SDS can mimic CF (borderline sweat electrolytes, recurrent lower respiratory infections, pancreatic insufficiency) but diverge in trajectory and management. Over 42 years, our patient demonstrated: (1) recurrent infections, (2) persistent pancreatic insufficiency and (3) intermittent neutropenia.
Freda Yang +3 more
wiley +1 more source
Primary hypertrophic osteoarthropathy (pachydermoperiostosis): a case report
, 2007 Hypertrophic osteoarthropathy is characterized by digital clubbing and periosteal reaction of long bones. Most cases are associated with malignancy or other conditions such as congenital heart disease, liver cirrhosis, pulmonary fibrosis, biliary atresia,
Erturk, ENGİN +5 more
core +1 more source
Melancholic Face Since Puberty; A Rare Case Report Of Primary Hypertrophic Osteoarthropathy [PDF]
, 2022 Pachydermoperiostosis or Touraine-Solente-Gole syndrome is a rare genetic disorder that follows autosomal dominant pattern of inheritance, wherein males are more commonly affected than females.
Nudrath Kahkashan +3 more
core +1 more source