Results 161 to 170 of about 5,479,866 (221)

Des Herrn Justizrath Johann Peter Willebrand Kurze Grundsätze von Beförderung der gesellschaftlichen Glückseligkeit in den Städten

open access: yes
DES HERRN JUSTIZRATH JOHANN PETER WILLEBRAND KURZE GRUNDSÄTZE VON BEFÖRDERUNG DER GESELLSCHAFTLICHEN GLÜCKSELIGKEIT IN DEN STÄDTEN Des Herrn Justizrath Johann Peter Willebrand Kurze Grundsätze von Beförderung der gesellschaftlichen Glückseligkeit in den
Willebrand, Johann Peter, Liebe, ...
core  

A new treatment for von Willebrand's syndrome.

open access: yesThe Turkish journal of pediatrics, 1967
S Ozsoylu, B Corbacioğlu
openaire   +2 more sources

von Willebrand factor Ristocetin co-factor activity to von Willebrand factor antigen level ratio for diagnosis of acquired von Willebrand syndrome caused by aortic stenosis. [PDF]

open access: yesRes Pract Thromb Haemost
Okubo N   +36 more
europepmc   +1 more source

Therapeutic approaches to acquired von Willebrand syndrome

Expert Opinion on Investigational Drugs, 2000
Acquired von Willebrand syndrome (AVWS) is a rare acquired bleeding disorder similar to the congenital von Willebrand disease (VWD) in terms of laboratory findings. Diagnosis of AVWS can be very difficult, with treatment normally taking an empirical form.
Augusto B Federici, A B Federici
exaly   +3 more sources

Acquired von Willebrand Syndrome in Children

Hämostaseologie, 2022
AbstractAcquired von Willebrand syndrome (AVWS) is a rare bleeding disorder caused by various underlying diseases or conditions and should be distinguished from the inherited type of von Willebrand disease. AVWS is associated with underlying diseases such as cardiovascular, autoimmune, malignant, proliferative disorders, or with mechanical circulatory ...
Sandrock, Kirstin   +2 more
openaire   +3 more sources

Acquired von Willebrand syndrome (AvWS)

Vnitřní lékařství, 2022
Acquired von Willebrand syndrome (AvWS) is a rare bleeding disorder caused by von Willebrand factor (vWF) dysfunction of various types and severities. Clinical manifestations and differences in the intensity of bleeding are then given by the diversity of vWF disorders.
Petr, Drenko   +2 more
openaire   +2 more sources

The von Willebrand Syndrome

British Journal of Haematology, 1975
Summary. Five patients with an original diagnosis of von Willebrand's disease are described because their levels of factor VIII related protein, Ristocetin‐induced platelet aggregation and/or family studies differed from the main group of patients with classical von Willebrand's disease.
P, Stableforth   +3 more
openaire   +2 more sources

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