Results 101 to 110 of about 55,967 (276)

PO42 | Acquired Von Willebrad syndrome in patients with myeloproliferative syndrome: literature review and single-center experience

open access: yesBleeding, Thrombosis and Vascular Biology
Background and Aims: Acquired von Willebrand Syndrome (AvWS) is a rare bleeding disorder, exhibiting clinical and laboratory features similar to hereditary von Willebrand Disease (vWD).
doaj   +1 more source

Features of coronary heart disease in a cohort of tajik patients and the condition of the vascular endothelium in its different clinical forms

open access: yesВестник медицинского института «Реавиз»: Реабилитация, врач и здоровье
Relevance. In the Republic of Tajikistan, in recent years there has been a steady increase in cardiovascular diseases. In this regard, special attention is paid to coronary heart disease with its various manifestations, which can often cause permanent ...
F. A. Shukurov, M. S. Tabarov
doaj   +1 more source

International Practice Variation in Post‐Tonsillectomy Hemorrhage: A Survey Study of Pediatric Otolaryngologists

open access: yesWorld Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Background A significant complication of pediatric tonsillectomy is post‐tonsillectomy bleeding (PTB). Management within and outside of the operating room (OR) is not standardized. We consolidated international similarities and differences in PTB management.
Gina M. Spencer   +8 more
wiley   +1 more source

Oral Hygiene and Dentition Status in Patients with Congenital Hemorrhagic Disorders: A Comparative Study

open access: yesPesquisa Brasileira em Odontopediatria e Clínica Integrada, 2022
Objective: To compare the status of oral hygiene and dentition in patients with congenital hemorrhagic disorders with their age-matched healthy counterparts.
Mathangi Kumar   +3 more
doaj  

Von willebrand disease: An overview

open access: yesIndian Journal of Pharmaceutical Sciences, 2011
Most commonly inherited bleeding disorder, first described in Aland Islands by Erik von Willebrand. It occurs as a result of decrease in plasma levels or defect in von Willebrand factor which is a large multimeric glycoprotein. Monomers of this glycoprotein undergo N-glycosylation to form dimers which get arranged to give multimers. Binding with plasma
Bharati, K. Pavani, Prashanth, U. Ram
openaire   +3 more sources

Two causes of COVID‐19‐related myocardial injury‐associated cardiogenic shock: Myocarditis and microvascular thrombosis

open access: yes
ESC Heart Failure, Volume 12, Issue 2, Page 1514-1522, April 2025.
Takamasa Iwai   +4 more
wiley   +1 more source

In Vitro Hemocompatibility of the BiVACOR Total Artificial Heart in Continuous and Pulsatile Flow

open access: yesArtificial Organs, EarlyView.
BiVACOR's total artificial heart generates remarkably similar hemocompatibility when operated with a pulse or during continuous flow. Under both conditions, hemolysis and von Willebrand Factor multimers were similar to a commercial reference device after 6 h in vitro evaluation.
Antony P. McNamee   +6 more
wiley   +1 more source

Preliminary Study Of Von Willebrand Factor Profiles Of The Different Abo Blood Group Among Malay Population [PDF]

open access: yes, 2016
Di kalangan 28 juta penduduk Malaysia pada tahun 2010, sebanyak 0.002% pesakit von Willebrand dilaporkan dengan 63% daripadanya berbangsa Melayu.
Abdul Rahman, Rohaida
core  

Integrating Dialysis in Ex Situ Machine Perfusion: A Systematic Review and Meta‐Analysis of Outcomes

open access: yesArtificial Organs, EarlyView.
Dialysis‐enhanced EVMP effectively maintains biochemical homeostasis, potentially mitigating metabolic stress and extending perfusion duration. Functional outcomes varied depending on the organ type, with the most pronounced benefits observed in cardiac perfusion.
Yomna E. Dean   +12 more
wiley   +1 more source

Hemodynamic activation of von Willebrand factor in children with congenital heart diseases

open access: yesАкушерство, гинекология и репродукция
Quite complex and non-linear cellular and molecular mechanisms underlie hemostasis changes in patients with congenital heart diseases (CHD). Altered activity ratio between von Willebrand factor (vWF) and metalloproteinase ADAMTS-13 (a disintegrin and ...
K. A. Tokmakova   +2 more
doaj   +1 more source

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