Results 191 to 200 of about 185,950 (370)

Porphyromonas gingivalis GroEL exacerbates orthotopic allograft transplantation vasculopathy via impairment of endothelial cell function

Molecular Oral Microbiology, EarlyView.
Abstract Orthotopic allograft transplantation (OAT) is a significant approach to addressing organ failure. However, persistent immune responses to the allograft affect chronic rejection, which induces OAT vasculopathy (OATV) and organ failure. Porphyromonas gingivalis can infiltrate remote organs via the bloodstream, thereby intensifying the severity ...
Chien‐Sung Tsai, Chun‐Yao Huang, Yi‐Ting Tsai, Chun‐Ming Shih, Ze‐Hao Lai, Chen‐Wei Liu, Yi‐Wen Lin, Feng‐Yen Lin   +7 more
wiley   +1 more source

Diagnostic approach to von Willebrand disease.

Blood, 2015
C. Ng, D. Motto, J. Di Paola
semanticscholar   +1 more source

Coronary Spasm Due to Pulsed Field Ablation: A State‐of‐the‐Art Review

Pacing and Clinical Electrophysiology, EarlyView.
ABSTRACT With the ever‐growing population of patients undergoing cardiac ablation with pulsed electric fields, there is a need to understand secondary effects from the therapy. Coronary artery spasm is one such effect that has recently emerged as the subject of further investigation in electrophysiology literature.
David A. Ramirez, Kara Garrott, Ann Garlitski, Brendan Koop   +3 more
wiley   +1 more source

Managing Anesthesia for a Patient With Von Willebrand Disease: A Case Report. [PDF]

Cureus
Singavarapu J, Borodulina G.
europepmc   +1 more source

Congenital infiltrating lipoma of the upper limb in a patient with von Willebrand disease [PDF]

, 2000
Jose María Lasso, Agustı́n España, Isabel Zudaire, Enrique de Álava, Antonio Bazán   +4 more
openalex   +1 more source

Developments in the diagnostic procedures for von Willebrand disease

Journal of Thrombosis and Haemostasis, 2016
A. D. Jong, Jeroen C. J. Eikenboom
semanticscholar   +1 more source

Successful Treatment of Severe Purpura Fulminans With Anakinra

Pediatric Dermatology, EarlyView.
ABSTRACT Purpura fulminans (PF) is a rare, often fatal pediatric condition characterized by intravascular thrombosis and hemorrhagic infarction of the skin. A timely diagnosis and treatment are paramount to prevent the involvement of internal organs, causing disseminated intravascular coagulation and gangrene of the extremities.
Francesco Zulian, Luca Spiezia, Antonio Amabile, Francesca Tirelli, Alessandra Meneghel   +4 more
wiley   +1 more source

Rewriting the script: gene therapy and genome editing for von Willebrand Disease. [PDF]

Front Genome Ed
Barraclough A, Bär I, van Duijl T, Fijnvandraat K, Eikenboom JCJ, Leebeek FWG, Bierings R, Voorberg J, Trasanidou D.   +8 more
europepmc   +1 more source

Study of von Willebrand factor, antithrombin III and protein C in patients with cerebrovascular disease.

, 1988
Akihiro Ihara, Yasuki Kobayashi, Tadao Morimoto, Yasuaki NOMA, Kazunari Oda, Ryuji Yamashita, Masakaze Nakata, Kingo Fujimura, Atsushi Kuramoto   +8 more
openalex   +2 more sources

Von Willebrand Disease in a Thoroughbred Mare and Foal [PDF]

, 2001
Rhonda A. Rathgeber, Marjory B. Brooks, Fairfield T. Bain, T. D. Byars   +3 more
openalex   +1 more source