Results 211 to 220 of about 79,317 (281)

A Duality Between Surface Charge and Work Function in Scanning Kelvin Probe Microscopy

open access: yesAdvanced Materials Interfaces, Volume 12, Issue 19, October 6, 2025.
Scanning Kelvin probe microscopy (SKPM) is a powerful technique for macroscopic imaging of the electrostatic potential above a surface, providing insight into sample work function and charge variations. General relationships are derived connecting the measured SKPM voltage image and the underlying work function variation or charge pattern.
Isaac C.D. Lenton   +3 more
wiley   +1 more source

Anti‐ADAMTS13 Antibodies Trajectory is Associated With ADAMTS13 Recovery in Immune‐Mediated TTP

open access: yesAmerican Journal of Hematology, Volume 100, Issue 10, Page 1736-1746, October 2025.
Anti‐ADAMTS13 IgG antibodies titer trajectory from baseline to day 7–14 post‐TPE as a reliable approach to identify iTTP patients at risk of late response to the triplet therapy regimen. ABSTRACT Current triplet regimens associating therapeutic plasma exchange (TPE), immunosuppression with corticosteroids and rituximab, and caplacizumab have ...
Marie Robert   +80 more
wiley   +1 more source

Acquired von Willebrand syndrome in children. [PDF]

open access: yesRes Pract Thromb Haemost
Favaloro EJ, Pasalic L.
europepmc   +1 more source

VWF excess and ADAMTS13 deficiency: a unifying pathomechanism linking inflammation to thrombosis in DIC, malaria, and TTP [PDF]

open access: green, 2014
Michael Schwameis   +4 more
openalex   +1 more source

Emerging Strategies for Platelet‐Modified Nanoparticles in Targeted Tumor Therapy

open access: yesAdvanced NanoBiomed Research, Volume 5, Issue 10, October 2025.
This review highlights innovative strategies using platelet‐modified nanoparticles to target tumors more precisely. By mimicking platelet functions, these biomimetic carriers improve tumor homing, enhance drug delivery, and reduce immune clearance.
Chunyu Bai   +5 more
wiley   +1 more source

A Novel Homozygous GFI1B Mutation in Siblings With Thrombocytopenia and Bleeding Tendency

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
Pedigree chart showing affected siblings. ABSTRACT Platelet type bleeding disorder 17 (OMIM #187900) is a type of “gray platelet syndrome” and occurs due to a mutation in the GFI1B gene on chromosome 9q34.13. Patients usually present with a history of easy bleeding tendencies, recurrent epistaxis or gum bleeding, and rarely with severe hemorrhage, and ...
Shova Aryal   +3 more
wiley   +1 more source

Plasmin-mediated proteolysis of von Willebrand factor in patients with acute and chronic liver disease. [PDF]

open access: yesRes Pract Thromb Haemost
El Otmani H   +6 more
europepmc   +1 more source

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