Suchergebnisse - "Nurden, Paquita"

PubPharm (21)

1

Healing through the lens of immunothrombosis : Biology-inspired, evolution-tailored, and human-engineered biomimetic therapies

enthalten in: Biomaterials | 2021

von Padilla, S. | Nurden, A. | Prado, R. | +2

2

Inherited platelet diseases with normal platelet count : phenotypes, genotypes and diagnostic strategy

enthalten in: Haematologica | 2021

von Nurden, P. | Stritt, S. | Favier, R. | +1

3

Inherited thrombocytopenias : history, advances and perspectives

enthalten in: Haematologica | 2020

von Nurden, A. | Nurden, P.

4

Autologous fibrin scaffolds : When platelet- and plasma-derived biomolecules meet fibrin

enthalten in: Biomaterials | 2019

von Anitua, E. | Nurden, P. | Prado, R. | +2

5

Should any genetic defect affecting α-granules in platelets be classified as gray platelet syndrome?

enthalten in: American journal of hematology | 2016

von Nurden, A. | Nurden, P.

6

Congenital platelet disorders and understanding of platelet function

enthalten in: British journal of haematology | 2014

von Nurden, A. | Nurden, P.

7

Understanding the genetic basis of Glanzmann thrombasthenia : implications for treatment

enthalten in: Expert review of hematology | 2012

von Nurden, A. | Pillois, X. | Nurden, P.

8

Glanzmann thrombasthenia : a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models

enthalten in: Blood | 2011

von Nurden, A. | Fiore, M. | Nurden, P. | +1

9

Glanzmann thrombasthenia-like syndromes associated with Macrothrombocytopenias and mutations in the genes encoding the αIIbβ3 integrin

enthalten in: Seminars in thrombosis and hemostasis | 2011

von Nurden, A. | Pillois, X. | Fiore, M. | +2

10

Are bone defects in rare patients with Glanzmann's thrombasthenia associated with ITGB3 or ITGA2B mutations?

enthalten in: Platelets | 2011

von Nurden, A. | Fiore, M. | Nurden, P. | +2