Results 151 to 160 of about 151,232 (337)

PHENOTYPIC STUDY AND MOLECULA ANALYSIS OF VON WILLEBRAND TYPE 1 PATIENTS

Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2006
BACKGROUND & OBJECTIVE: Von willebrand disease (VWD) is the most common bleeding disorder caused by von willbrand factor (VWF) deficiency and autosomal dominance inheritance pattern. It is divided into three types, one and three (quantitative) and type 2
SMB Hashemi Soteh, N Rezaei, A Goodeve
doaj  

Von Willebrand factor propeptide in severe coronavirus disease 2019 (COVID‐19): evidence of acute and sustained endothelial cell activation [PDF]

, 2020
Soracha E. Ward, Gerard F. Curley, Michelle Lavin, Helen Fogarty, Ellie Karampini, Natalie McEvoy, Jennifer Clarke, Maria Boylan, Razi Alalqam, Amy P Worrall, Claire Kelly, Eoghan de Barra, Siobhán Glavey, Clíona Ní Cheallaigh, Colm Bergin, Ignacio Martín‐Loeches, Liam Townsend, Patrick Mallon, Jamie M. O’Sullivan, James S. O’Donnell, the Irish COVID‐19 Vasculopathy Study (ICVS) Investigators   +20 more
openalex   +1 more source

Von Willebrand disease [PDF]

Clinical Medicine, 2007
openaire   +2 more sources

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

von Willebrand factor and occlusive arterial thrombosis. A study in normal and von Willebrand's disease pigs with diet-induced hypercholesterolemia and atherosclerosis.

, 1990
Timothy C. Nichols, Dwight A. Bellinger, David A. Tate, Robert L. Reddick, Marjorie S. Read, Gary G. Koch, K. M. Brinkhous, Thomas R. Griggs   +7 more
openalex   +1 more source

von Willebrand disease biology [PDF]

Haemophilia, 2012
Blomback, M., Eikenboom, J., Lane, D., Denis, C., Lillicrap, D.   +4 more
openaire   +3 more sources

Validating the Online Self‐Administered Bleeding Assessment Tool (Self‐BAT) as a Screening Tool for Bleeding Disorders

Haemophilia, EarlyView.
Veronica DeYoung, Julie Grabell, Wilma Hopman, Megan Chaigneau, Maria Avgeropoulos, Paula James   +5 more
wiley   +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

Shear stress activation of platelet glycoprotein IIb/IIIa plus von Willebrand factor causes aggregation: filter blockage and the long bleeding time in von Willebrand's disease [PDF]

, 1987
JR O'Brien, G P Salmon
openalex   +1 more source

Chronic Morel‐Lavallée Lesion in a Pediatric Competitive Dancer: A Case Report and Literature Review

Pediatric Dermatology, EarlyView.
ABSTRACT Morel‐Lavallée lesions (MLLs) are rare internal degloving injuries resulting from shearing trauma, with few reported cases in the pediatric population. We present the case of a 16‐year‐old female competitive dancer with persistent right knee pain, skin atrophy, and ecchymosis after trauma sustained during a national dance competition, with MRI
Cameron Coakes, Kent Axcell, Andrea L. Zaenglein, Timothy Hahn   +3 more
wiley   +1 more source