Results 61 to 70 of about 3,722 (185)

Collagenase treatment does not impair fiber contractile function in muscle biopsies from children with cerebral palsy

open access: yesPhysiological Reports, Volume 13, Issue 21, November 2025.
Abstract Cerebral palsy (CP) often presents with increased passive stiffness of the skeletal muscles, primarily due to increased collagen in the extracellular matrix. Collagenase from Clostridium histolyticum (CCH), an enzyme that degrades collagen, is used clinically to treat fibrotic conditions such as Dupuytren's contracture and Peyronie's disease ...
Faizan Syed   +5 more
wiley   +1 more source

The impact of comorbidities on surgical outcomes in Dupuytren’s disease

open access: yesJournal of Plastic Surgery and Hand Surgery
Introduction: Dupuytren’s disease is a progressive fibroproliferative condition characterized by collagen deposition and the formation of fibrous cords along the palmar fascia and flexor tendons of the fingers.
Mehmet Yalçın   +3 more
doaj   +1 more source

Impact of a multidisciplinary approach in enteropathic spondyloarthritis patients [PDF]

open access: yes, 2016
Spondyloarthritis (SpA) and inflammatory bowel disease (IBD) are chronic autoinflammatory diseases that partially share the genetic predisposition and the unchecked inflammatory response linking the gut to the joints.
Ascolani, M   +11 more
core   +1 more source

IVUS Guided Ostial Lesion Preparation With Sequential Cutting Balloon Inflations and Stent Placement—The ORCAS Technique

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT The ORCAS technique highlights the potential value of continuous intracoronary imaging during key procedural steps such as plaque preparation and ostial stent implantation. Real‐time IVUS guidance may support more precise assessment and execution, possibly improving procedural accuracy and consistency in complex aorto‐ostial lesions ...
Claudiu Ungureanu   +6 more
wiley   +1 more source

Pathomorphological characteristics of Dupuytren's contracture in a patient with liver disease (case report) [PDF]

open access: yesГений oртопедии, 2019
Objective To detect pathomorphological characteristics of the palmar aponeurosis in Dupuytren’s contracture in patients with liver disease. Material and methods The review included a medical record and histological findings of surgical specimen of a 60 ...
Natalia A. Shchudlo   +6 more
doaj   +1 more source

Uncovering regulatory B‐cell features associated with regulatory T‐cell expansion and global T‐cell exhaustion in Waldenström macroglobulinemia Myd88L252P‐like lymphoplasmacytic lymphomas

open access: yesHemaSphere, Volume 9, Issue 10, October 2025.
Abstract Waldenström's macroglobulinemia (WM) is a rare, indolent lymphoproliferative disorder, genetically characterized by the presence of the L265P mutation in the MYD88 gene in almost all cases, resulting in constitutive activation of NF‐kappa B (NF‐κB). Despite its slow progression, WM remains incurable due to the lack of specific treatments.
Quentin Lemasson   +7 more
wiley   +1 more source

Dupuytren’s Fasciectomy: Surgical Pearls in Planning and Dissection

open access: yesPlastic and Reconstructive Surgery, Global Open, 2020
Summary:. Fasciectomy remains the mainstay of surgical treatment for Dupuytren’s disease at many units worldwide, particularly in cases of recurrence after aponeurotomy or enzymatic fasciotomy.
Pennylouise Hever, MBChB, MRCS   +2 more
doaj   +1 more source

Monoartritis gotosa de muñeca asociada a necrosis del semilunar: a propósito de un caso clínico [PDF]

open access: yes, 1994
Se presenta un caso de monoartritis de muñeca asociada a imágenes radiológicas de necrosis avascular del semilunar que, tras biopsia de la sinovial, se diagnostica de artritis gotosa. Esta asociación es rara. La alteración metabólica que se produce en la
Mackenney Carrasco, Enrique   +1 more
core  

Recent Surgical and Medical Advances in the Treatment of Dupuytren’s Disease - A Systematic Review of the Literature [PDF]

open access: yes, 2012
Dupuytren’s disease (DD) is a type of fibromatosis which progressively results in the shortening and thickening of the fibrous tissue of the palmar fascia. This condition which predominantly affects white-northern Europeans has been identified since 1614.
Abe Y   +57 more
core   +2 more sources

Causes of Death and Comorbidities in Adult Patients With Late‐Onset Pompe Disease: A French Pompe Registry Retrospective Study

open access: yesEuropean Journal of Neurology, Volume 32, Issue 10, October 2025.
ABSTRACT Background and Objectives Mortality in Late‐Onset Pompe Disease (LOPD) has been associated with the rapid progression of respiratory and motor impairment. However, an in‐depth approach to the exact causes of death in these patients is still lacking.
Diana Maria Chitimus   +61 more
wiley   +1 more source

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