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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
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1990 1
1991 1
1993 1
1994 1
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1997 3
1998 4
2001 2
2002 5
2003 3
2004 3
2005 6
2006 3
2007 2
2008 4
2009 5
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2015 12
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140 results

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Page 1
Glanzmann thrombasthenia: genetic basis and clinical correlates.
Botero JP, Lee K, Branchford BR, Bray PF, Freson K, Lambert MP, Luo M, Mohan S, Ross JE, Bergmeier W, Di Paola J; ClinGen Platelet Disorder Variant Curation Expert Panel. Botero JP, et al. Haematologica. 2020 Apr;105(4):888-894. doi: 10.3324/haematol.2018.214239. Epub 2020 Mar 5. Haematologica. 2020. PMID: 32139434 Free PMC article. Review.
Glanzmann thrombasthenia (GT) is an autosomal recessive disorder of platelet aggregation caused by quantitative or qualitative defects in integrins alphaIIb and beta3. ...
Glanzmann thrombasthenia (GT) is an autosomal recessive disorder of platelet aggregation caused by quantitative or qualitative …
Inherited platelet disorders.
Sandrock-Lang K, Wentzell R, Santoso S, Zieger B. Sandrock-Lang K, et al. Hamostaseologie. 2016 Aug 3;36(3):178-86. doi: 10.5482/HAMO-14-11-0067. Epub 2015 Feb 24. Hamostaseologie. 2016. PMID: 25707719 Review.
Inherited platelet disorders can be classified according to their platelet defects: receptor defects (adhesion or aggregation), secretion disorder, and cytoskeleton defects. The best characterized platelet receptor defects are Glanzmann thrombasthenia (integrin alph …
Inherited platelet disorders can be classified according to their platelet defects: receptor defects (adhesion or aggregation), secretion di …
Glanzmann thrombasthenia.
Nurden AT. Nurden AT. Orphanet J Rare Dis. 2006 Apr 6;1:10. doi: 10.1186/1750-1172-1-10. Orphanet J Rare Dis. 2006. PMID: 16722529 Free PMC article. Review.
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by lack of platelet aggregation. ...
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characte …
Inherited platelet disorders.
Nurden AT, Freson K, Seligsohn U. Nurden AT, et al. Haemophilia. 2012 Jul;18 Suppl 4:154-60. doi: 10.1111/j.1365-2516.2012.02856.x. Haemophilia. 2012. PMID: 22726100 Review.
Platelet defects extend from the absence or malfunctioning of adhesion (GPIb-IX-V, Bernard-Soulier syndrome) or aggregation receptors (integrin alphaIIbbeta3, Glanzmann thrombasthenia) to defects of primary receptors for soluble agonists, secretion from storage orga …
Platelet defects extend from the absence or malfunctioning of adhesion (GPIb-IX-V, Bernard-Soulier syndrome) or aggregation receptors (integ …
Should studies on Glanzmann thrombasthenia not be telling us more about cardiovascular disease and other major illnesses?
Nurden AT. Nurden AT. Blood Rev. 2017 Sep;31(5):287-299. doi: 10.1016/j.blre.2017.03.005. Epub 2017 Apr 4. Blood Rev. 2017. PMID: 28395882 Review.
Glanzmann thrombasthenia (GT) is a rare inherited bleeding disorder caused by loss of alphaIIbbeta3 integrin function in platelets. ...
Glanzmann thrombasthenia (GT) is a rare inherited bleeding disorder caused by loss of alphaIIbbeta3 integrin function in plate …
Inherited platelet disorders including Glanzmann thrombasthenia and Bernard-Soulier syndrome.
Diz-Küçükkaya R. Diz-Küçükkaya R. Hematology Am Soc Hematol Educ Program. 2013;2013:268-75. doi: 10.1182/asheducation-2013.1.268. Hematology Am Soc Hematol Educ Program. 2013. PMID: 24319190 Review.
This review summarizes the classification and clinical and molecular characteristics of known IPDs, including Bernard-Soulier syndrome and Glanzmann thrombasthenia, with a focus on current challenges in the laboratory diagnosis and management of bleeding in these pa …
This review summarizes the classification and clinical and molecular characteristics of known IPDs, including Bernard-Soulier syndrome and …
Glanzmann thrombasthenia: an update.
Franchini M, Favaloro EJ, Lippi G. Franchini M, et al. Clin Chim Acta. 2010 Jan;411(1-2):1-6. doi: 10.1016/j.cca.2009.10.016. Epub 2009 Oct 23. Clin Chim Acta. 2010. PMID: 19854165 Review.
Glanzmann thrombasthenia (GT) is a rare autosomal recessive disorder characterized by qualitative or quantitative abnormalities of the platelet membrane glycoprotein (GP) IIb/IIIa. ...
Glanzmann thrombasthenia (GT) is a rare autosomal recessive disorder characterized by qualitative or quantitative abnormalitie …
Inherited Bleeding Disorders in the Obstetric Patient.
Bannow BS, Konkle BA. Bannow BS, et al. Transfus Med Rev. 2018 Oct;32(4):237-243. doi: 10.1016/j.tmrv.2018.06.003. Epub 2018 Jul 12. Transfus Med Rev. 2018. PMID: 30097224 Review.
For factor deficiencies in which no specific concentrate is available, such as factors II (prothrombin) and V, prothrombin complex concentrate or fresh frozen plasma may be used, and for platelet defects or deficiencies, such as Glanzmann thrombasthenia or Bernard-S …
For factor deficiencies in which no specific concentrate is available, such as factors II (prothrombin) and V, prothrombin complex concentra …
Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy.
Nurden P, Stritt S, Favier R, Nurden AT. Nurden P, et al. Haematologica. 2021 Feb 1;106(2):337-350. doi: 10.3324/haematol.2020.248153. Haematologica. 2021. PMID: 33147934 Free PMC article. Review.
Inherited platelet disorders resulting from platelet function defects and a normal platelet count cause a moderate or severe bleeding diathesis. Since the description of Glanzmann thrombasthenia resulting from defects of ITGA2B and ITGB3, new inherited platelet diso …
Inherited platelet disorders resulting from platelet function defects and a normal platelet count cause a moderate or severe bleeding diathe …
Glanzmann thrombasthenia: state of the art and future directions.
Nurden AT, Pillois X, Wilcox DA. Nurden AT, et al. Semin Thromb Hemost. 2013 Sep;39(6):642-55. doi: 10.1055/s-0033-1353393. Epub 2013 Aug 8. Semin Thromb Hemost. 2013. PMID: 23929305 Free PMC article. Review.
Glanzmann thrombasthenia (GT) is the principal inherited disease of platelets and the most commonly encountered disorder of an integrin. ...
Glanzmann thrombasthenia (GT) is the principal inherited disease of platelets and the most commonly encountered disorder of an …
140 results