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Nature Communications|July 17, 2014
Identification of platelet function defects by multi-parameter assessment of thrombus formationSusanne M de Witt, Frauke Swieringa, Rachel Cavill, et al.
The Journal of Experimental Medicine|March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutationNour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Scientific Reports|July 11, 2020
Impaired iloprost-induced platelet inhibition and phosphoproteome changes in patients with confirmed pseudohypoparathyroidism type Ia, linked to genetic mutations in GNASFrauke Swieringa, Fiorella A Solari, Oliver Pagel, et al.
Hemasphere|March 26, 2025
Mild or moderate hemophilia is not always a mild or moderate bleeding disorder: Back to the clinical phenotypeFrancesco Rodeghiero, Lisanna Ghiotto, Luca Pontalto, et al.
Blood|February 14, 2013
The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2Birthe Jessen, Sebastian F N Bode, Sandra Ammann, et al.
Molecular Biology of the Cell|December 12, 2002
Mammalian septins nomenclatureIan G Macara, Richard Baldarelli, Christine M Field, et al.
Blood Advances|January 26, 2021
Neutrophil specific granule and NETosis defects in gray platelet syndromeCathelijn E M Aarts, Kate Downes, Arie J Hoogendijk, et al.
Haematologica|September 28, 2019
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT StudyFrancesco Paciullo, Loredana Bury, Patrizia Noris, et al.
Haematologica|April 8, 2017
Bleeding risk of surgery and its prevention in patients with inherited platelet disordersSara Orsini, Patrizia Noris, Loredana Bury, et al.
Human Mutation|June 18, 2014
Spectrum of the mutations in Bernard-Soulier syndromeAnna Savoia, Shinji Kunishima, Daniela De Rocco, et al.
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