Results 71 to 80 of about 13,243 (286)

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States [PDF]

, 2016
Von Willebrand disease (VWD) is the most common inherited bleeding disorder, and type 1 VWD is the most common VWD variant. Despite its frequency, diagnosis of type 1 VWD remains the subject of much debate.
Abshire, T.C., Bellissimo, D.B., Boggio, L.N., Christopherson, P.A., Dasgupta, M., Flood, V.H., Friedman, K.D., Gill, J.C., Goodeve, A.C., Gruppo, R.A., Haberichter, S.L., Hoffmann, R.G., Hoots, W.K., James, P.D., Leissinger, C., Lentz, S.R., Lillicrap, D., Lusher, J.M., Manco-Johnson, M.J., Montgomery, K.T., Montgomery, R.R., Peake, I.R., Ragni, M.V., Shapiro, A.D., Udani, R.A.   +24 more
core   +1 more source

Predictive accuracy of diagnostic tests for excessive bleeding in cardiac surgery: The COPTIC‐C study

Transfusion, EarlyView.
Abstract Background We tested the hypothesis that the addition of biomarkers of multimorbidity and biological aging would improve the predictive accuracy of point‐of‐care viscoelastometry or laboratory tests of coagulation for clinically important bleeding following cardiac surgery.
Weiqi Liao, Robert Grant, Florence Y. Lai, Hardeep Aujla, Marcin Wozniak, Hasmukh R. Patel, Laura Green, Andrew Mumford, Gavin J. Murphy   +8 more
wiley   +1 more source

Influences of ABO blood group, age and gender on plasma coagulation factor VIII, fibrinogen, von Willebrand factor and ADAMTS13 levels in a Chinese population [PDF]

PeerJ, 2017
Background ABO blood group is a hereditary factor of plasma levels of coagulation factor VIII (FVIII) and von Willebrand factor (VWF). Age and gender have been shown to influence FVIII, VWF, fibrinogen (Fbg), and ADAMTS13 (A disintegrin and ...
Zongkui Wang, Miaomiao Dou, Xi Du, Li Ma, Pan Sun, Haijun Cao, Shengliang Ye, Peng Jiang, Fengjuan Liu, Fangzhao Lin, Rong Zhang, Changqing Li   +11 more
doaj   +2 more sources

Increased plasma von Willebrand factor antigen levels but normal von Willebrand factor cleaving protease (ADAMTS13) activity in preeclampsia. [PDF]

, 2009
The activity of ADAMTS13, the von Willebrand factor (VWF) cleaving protease is low in several conditions, including HELLP (haemolysis, elevated liver enzymes, and low platelet count) syndrome.
Bõze, Tamás, Cervenak, László, Derzsy, Zoltán, Gombos, Tímea, Hársfalvi, Jolán, Makó, Veronika, Molvarec, Attila, Prohászka, Zoltán, Rigó, János, Udvardy, Miklós László   +9 more
core   +1 more source

Essential Thrombocythemia's Role in the Complex Landscape of Vasculitis: A Case Report

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Peripheral gangrenes have been sporadically documented as the initial presentation of essential thrombocythemia (ET), as exemplified in the preceding case reports. Nevertheless, the prevalence of vasculitis‐induced skin problems as the primary indication of ET has not been extensively examined.
Mohammad Reza Jafari Nakhjavani, Seyedeh‐Tarlan Mirzohreh, Sousan Kolahi, Mehrzad Hajialilo, Mehdi Jafarpour, Arezou Ghassembaglou, Mir Ali Sattary Oskouie, Tala Pourlak, Sepideh Tahsini Tekantapeh   +8 more
wiley   +1 more source

Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia

The Turkish Journal of Pediatrics, 1995
Platelet function was studied in a child with myelodysplastic syndrome (MDS: refractory anemia with an excess of blasts) and a child with acute myeloblastic leukemia (AML-M6) associated with trilineage myelodysplasia (TMDS).
G Hiçsönmez, F Gümrük, M Cetin, N Ozbek, M Tuncer, T Gürsel   +5 more
doaj  

Lymphoma‐associated acquired von Willebrand syndrome responsive to splenectomy: A case report

eJHaem, 2022
A previously healthy 33‐year‐old female presented with a large hematoma over her right knee after kneeling. She was found to have pancytopenia and massive splenomegaly.
Fatima Khadadah, Natasha Rupani, Jordan Scott, Martina Trinkaus, Jerome Teitel, Michelle Sholzberg   +5 more
doaj   +1 more source

MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations [PDF]

, 2013
MYH9-related disease (MYH9-RD) is a rare autosomal dominant syndromic disorder caused by mutations in MYH9, the gene encoding for the heavy chain of non-muscle myosin IIA (myosin-9).
Balduini, Carlo L., Barozzi, Serena, Bottega, Roberta, de Rocco, Daniela, Glembotsky, Ana Claudia, Heller, Paula Graciela, Noris, Patrizia, Pastore, Annalisa, Pecci, Alessandro, Pergantou, Helen, Platokouki, Helen, Savoia, Anna, Zieger, Barbara   +12 more
core   +1 more source

Complications at Diagnosis of Pediatric Chronic Myeloid Leukemia in Chronic Phase

Pediatric Blood &Cancer, Volume 72, Issue 10, October 2025.
ABSTRACT Chronic myeloid leukemia (CML) is uncommon during the first two decades of life, resulting in limited experience of pediatricians in handling this leukemia. This is even more true when it comes to managing rare complications at the time of diagnosis.
Nirmalya Roy Moulik, Uma Athale, Markus Metzler, Frederic Millot, Meinolf Suttorp   +4 more
wiley   +1 more source

INVESTIGATION OF RISTOCETIN-INDUCED PLATELET AGGREGATION, PARAMETERS OF VON WILLEBRAND FACTOR AND THE COAGULATION FACTOR VIII AT ESSENTIAL ARTERIAL HYPERTENSION IN CHILDREN

Acta Biomedica Scientifica, 2014
Ristocetin-induced platelet aggregation, von Willebrand factor and coagulation factor VIII of 170 children with essential arterial hypertension and 40 healthy children were investigated.
M. V. Gomellya
doaj