» Articles » PMID: 4864595

Studies of Platelet Function and Proteins in 3 Patients with Glanzmann's Thrombasthenia

Overview
Journal J Lab Clin Med
Publisher Elsevier
Date 1968 Jan 1
PMID 4864595
Citations 17
Authors
Affiliations
Soon will be listed here.
Citing Articles

Clinical Management of a Rare Hereditary Bleeding Disorder in an Adult: Glanzmann Thrombasthenia.

Mecca R, Senthil N, Lakshmanan S, Anna Anil A Cureus. 2024; 16(10):e72391.

PMID: 39588442 PMC: 11586241. DOI: 10.7759/cureus.72391.


Haemorrhagic Disorders Due to Functional Abnormalities of Platelets.

Hardisty R J R Coll Physicians Lond. 2019; 3(2):182-192.

PMID: 30667699 PMC: 5367099.


Historical perspective and future directions in platelet research.

Coller B J Thromb Haemost. 2011; 9 Suppl 1:374-95.

PMID: 21781274 PMC: 3163479. DOI: 10.1111/j.1538-7836.2011.04356.x.


Glanzmann's thrombasthenia: report of a case and review of the literature.

Sebastiano C, Bromberg M, Breen K, Hurford M Int J Clin Exp Pathol. 2010; 3(4):443-7.

PMID: 20490335 PMC: 2872751.


Inhibition of platelet-mediated, tissue factor-induced thrombin generation by the mouse/human chimeric 7E3 antibody. Potential implications for the effect of c7E3 Fab treatment on acute thrombosis and "clinical restenosis".

Reverter J, Beguin S, Kessels H, Kumar R, Hemker H, Coller B J Clin Invest. 1996; 98(3):863-74.

PMID: 8698879 PMC: 507497. DOI: 10.1172/JCI118859.