Results 1 to 10 of about 5,929 (175)

Identification of novel plasma proteomic biomarkers of Dupuytren disease. [PDF]

PLoS ONE
Dupuytren Disease (DD) is a chronic progressive disease that can cause disabling hand deformities. The most common treatments have either high complication rates or high early recurrence rates.
Blake Hummer, Paola Sebastiani, Anastasia Leshchyk, Anastasia Gurinovich, Cecilie Bager, Morten Karsdal, Signe Nielsen, Charles Eaton   +7 more
doaj   +2 more sources

Development and Validation of Algorithms for Systemic Sclerosis Identification in Electronic Health Record Data. [PDF]

ACR Open Rheumatol
Objective The aim of this study was to develop and validate International Classification of Diseases (ICD) code–based algorithms for identifying systemic sclerosis (SSc) cases within electronic health record (EHR) data and to evaluate algorithm performance. Methods We identified patients with at least one ICD, Ninth Revision (ICD‐9)/ICD‐10 code for SSc
Ozen G, O'Rorke M, Romitti P, Domsic R.
europepmc   +2 more sources

Paediatric Dupuytren′s disease

Indian Journal of Plastic Surgery, 2011
Dupuytren′s disease of the hand has only been rarely reported in children and is rarer still in infants. Only a few histologically confirmed diagnoses are found in literature.
Pradeoth Mukundan Korambayil, Anto Francis Padikala   +1 more
doaj   +4 more sources

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study. [PDF]

Hemasphere
HemaSphere, Volume 10, Issue 5, May 2026.
Benoit A, Pages J, Szepetowski S, Agouti I, Thuret I, Le Roux E, Badens C, Brousse V, NaThalY Network, Mathey C, Bey L, Lucchini MJ, Li Thio Te V, Garidi R, Garcon L, Orvain C, Brasme JF, Reynes C, Belloy M, Durin J, Alhindy O, Sabbagh L, Slama B, Sanchez A, Moulin A, Belgodere D, Benjemia L, Simon P, Oziol E, Aladjidi N, Huguenin Y, Jubert C, Forcade E, Duffau P, Maakaroun A, Lachenal F, Pegon C, Odievre MH, Petitdidier C, Atmani S, Raqbi F, Pondarre C, Youn J, Kamdem A, Bachir D, Bartolucci P, De Luna G, Habibi A, Fois E, Leblanc A, Dides PY, Makowski C, Armari C, Elenga N, Chantalat-Auger C, Driss F, Zenchri F, Guitton C, Jehanne M, Stoven C, Chaminade A, Gourdon S, Reguerre Y, Randriamalala E, Paumier-Bonjour V, Besancon-Bergelin A, Lambilliotte A, Bruno B, Gonzales F, Barbati M, Carpentier B, Piguet C, Touati M, Hot A, Barraco F, Cannas G, Virot E, Fort R, Ducoux G, Clavel HD, Kebaili K, Garnier N, Renard C, Bertrand Y, Peugnet AL, Halfon-Domenech C, Diakiesse J, Agbo-Kpati KP, Ravet N, Thuret I, Szepetowski S, Jean E, De Sainte Marie B, Meunier B, Faucher B, Muszlak M, Chamouine A, Garou A, Masserot-Lureau C, Schneider JM, Dorvaux V, Carassou P, Andriamihaja H, Lalande M, Mahe P, Sirvent A, Martinez PA, Bertchansky I, Eisenmann JC, Masseau A, Couec ML, Rialland F, Rohrlich PS, Baron-Joly S, Conde M, Dossier A, Brousse V, Yakouben K, Benkerrou M, Ithier G, Missud F, Dalle JH, Koehl B, Holvoet L, Ribeil JA, Joseph L, Cavazzana M, De Montalembert M, Neven B, Moshous D, Taylor M, Allali S, Varet B, Socie G, Xhaard A, De La Tour RP, Leblanc T, Boissel N, Robin M, Dhedin N, Girot R, Mattioni S, Lionnet F, Donadieu J, Leverger G, Fasola S, Arlet JB, Manoli C, Etienne-Julan M, Bernit E, Gellen-Dautremer J, Eyssette S, Blondin G, Pluchart C, Nimubona S, Bonneau J, Bayart S, Pertuisel S, Collet B, Detourmignies L, Machin J, Wemeau M, De Tourmigni L, Vannier JP, Filhon B, Dumesnil C, Lahary A, Schneider P, Ngo S, Malric A, Schoeny M, Berger C, Guichard I, Desbree A, Stephan JL, David A, Paillard C, Salmon A, Ame S, Gestas P, Besnard M, Castex MP, Plat-Wilson G, Cougoul P, Pasquet M, Serre J, Yvert M, Valentin JB, Duchene F, Mathieu S, Drouilly M, Detrait M, Pochon C, Phulpin A, Nathanson S.   +194 more
europepmc   +2 more sources

Langerhans Cell Histiocytosis and Mastocytosis: A Rare Association [PDF]

Dermatology Practical & Conceptual
Romain Boisseau, Lea Scaramuzzino, Grégory Bosphore, Kim Heang Ly   +3 more
doaj   +2 more sources

Analysis of a National Database Investigating Development of Trigger Finger after Treatment of Dupuytren Disease

Plastic and Reconstructive Surgery, Global Open, 2023
Background:. Dupuytren disease is associated with inflammation and myofibroblast overgrowth, as is stenosing tenosynovitis (trigger finger). Both are linked with fibroblast proliferation, but a potential associative link between the diseases is unknown ...
Michael B. Gehring, MD, Ryan S. Constantine, MD, Elliot L. H. Le, MD, MBA, Brandon Wolfe, BA, Mark A. Greyson, MD, Matthew L. Iorio, MD   +5 more
doaj   +1 more source

Fibroproliferative disorders and diabetes: Understanding the pathophysiologic relationship between Peyronie’s disease, Dupuytren disease and diabetes

Endocrinology, Diabetes & Metabolism, 2021
Introduction Fibrosis is characterized by dysregulation and accumulation of extracellular matrix. Peyronie's disease and Dupuytren disease are fibroproliferative disorders of the tunica albuginea of the penis and fascia of the hand, respectively. Chronic
Martin K. Gelbard, Joel Rosenbloom
doaj   +1 more source

Suprapatellar Nail, Gold Standard in the treatment of Tibial fractures

Journal of the Foot & Ankle, 2023
RESUMEN introducción: El uso exclusivo de clavo suprapatelar para la osteosíntesis de las fracturas de tercio proximal de tibia se ha perdido con el tiempo, ampliándose su indicación para las fracturas de tibia en todos sus niveles.
Leando Casola, Matias Iglesias, Germán Matías-Joannas, Santiago Eslava, María José Martínez, Juan Manuel Gaillard, Guillermo Martin Arrondo   +6 more
doaj   +1 more source

The worldwide prevalence of the Dupuytren disease: a comprehensive systematic review and meta-analysis

Journal of Orthopaedic Surgery and Research, 2020
Background The Dupuytren disease is a benign fibroproliferative disorder that leads to the formation of the collagen knots and fibres in the palmar fascia.
Nader Salari, Mohammadbagher Heydari, Masoud Hassanabadi, Mohsen Kazeminia, Nikzad Farshchian, Mehrdad Niaparast, Yousef Solaymaninasab, Masoud Mohammadi, Shamarina Shohaimi, Alireza Daneshkhah   +9 more
doaj   +1 more source

Spontaneous community-acquired PVL-producing Staphylococcus aureus mediastinitis in an immunocompetent adult – a case report

BMC Infectious Diseases, 2020
Background Mediastinitis caused by hematogenous spread of an infection is rare. We report the first known case of community-acquired mediastinitis from hematogenous origin in an immunocompetent adult.
Josselin Brisset, Thomas Daix, Jérémy Tricard, Bruno Evrard, Philippe Vignon, Olivier Barraud, Bruno François   +6 more
doaj   +1 more source