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

Year Number of Results
1986 1
1987 1
1988 1
1989 2
1990 4
1991 1
1994 1
1998 3
1999 1
2000 1
2002 1
2003 1
2004 1
2005 1
2007 5
2008 4
2009 5
2011 1
2012 1
2013 5
2014 2
2015 2
2016 2
2017 2
2018 2
2019 1
2020 2
2021 3
2024 0

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51 results

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Page 1
Anti-alpha(IIb) beta(3) immunization in Glanzmann thrombasthenia: review of literature and treatment recommendations.
Fiore M, d'Oiron R, Pillois X, Alessi MC. Fiore M, et al. Br J Haematol. 2018 Apr;181(2):173-182. doi: 10.1111/bjh.15087. Epub 2018 Apr 2. Br J Haematol. 2018. PMID: 29611179 Free article. Review.
Glanzmann thrombasthenia (GT) is caused by inherited defects of the alpha(II)(b) beta(3) platelet glycoprotein. ...
Glanzmann thrombasthenia (GT) is caused by inherited defects of the alpha(II)(b) beta(3) platelet glycoprotein. ...
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's thrombasthenia: an overview.
Kannan M, Saxena R. Kannan M, et al. Clin Appl Thromb Hemost. 2009 Mar-Apr;15(2):152-65. doi: 10.1177/1076029608326165. Epub 2008 Oct 16. Clin Appl Thromb Hemost. 2009. PMID: 18930954 Free article. Review.
Glanzmann's thrombasthenia (GT) is an autosomal recessive inherited bleeding disorder due to a defect in platelet function. ...A patient with GT, with no possible causative mutations in GPIIb and GPIIIa genes, may harbor defects in a regulatory element affecting the
Glanzmann's thrombasthenia (GT) is an autosomal recessive inherited bleeding disorder due to a defect in platelet function. ..
Gene Therapy for Inherited Bleeding Disorders.
Arruda VR, Weber J, Samelson-Jones BJ. Arruda VR, et al. Semin Thromb Hemost. 2021 Mar;47(2):161-173. doi: 10.1055/s-0041-1722862. Epub 2021 Feb 26. Semin Thromb Hemost. 2021. PMID: 33636747 Free PMC article. Review.
Preclinical studies have also investigated gene transfer approaches for other rare inherited bleeding disorders, including factor VII deficiency, von Willebrand disease, and Glanzmann thrombasthenia. Here we review the successful gene therapy journey for hemophilia …
Preclinical studies have also investigated gene transfer approaches for other rare inherited bleeding disorders, including factor VII defici …
New Insights Into the Treatment of Glanzmann Thrombasthenia.
Poon MC, Di Minno G, d'Oiron R, Zotz R. Poon MC, et al. Transfus Med Rev. 2016 Apr;30(2):92-9. doi: 10.1016/j.tmrv.2016.01.001. Epub 2016 Jan 30. Transfus Med Rev. 2016. PMID: 26968829 Free article. Review.
Glanzmann thrombasthenia (GT) is a rare inherited autosomal recessive bleeding disorder of platelet function caused by a quantitative or qualitative defect of platelet membrane glycoprotein IIb/IIIa (integrin alphaIIbbeta3), a fibrinogen receptor required for platel
Glanzmann thrombasthenia (GT) is a rare inherited autosomal recessive bleeding disorder of platelet function caused by a quant
Surgical procedures in patients with Glanzmann's thrombasthenia: case series and literature review.
Ganapule A, Jain P, Abubacker FN, Korula A, Abraham A, Mammen J, George B, Mathews V, Srivastava A, Viswabandya A. Ganapule A, et al. Blood Coagul Fibrinolysis. 2017 Mar;28(2):171-175. doi: 10.1097/MBC.0000000000000524. Blood Coagul Fibrinolysis. 2017. PMID: 27273143 Review.
Glanzmann's thrombasthenia is a rare platelet function disorder with an autosomal recessive pattern of inheritance. Achieving haemostasis in such patients who undergo surgical procedures always poses a significant challenge. Herein we report six cases of Glanzman
Glanzmann's thrombasthenia is a rare platelet function disorder with an autosomal recessive pattern of inheritance. Achieving
Inherited bleeding disorders.
Blanchette VS, Sparling C, Turner C. Blanchette VS, et al. Baillieres Clin Haematol. 1991 Apr;4(2):291-332. doi: 10.1016/s0950-3536(05)80162-3. Baillieres Clin Haematol. 1991. PMID: 1912663 Review.
Comparable platelet disorders include the inherited thrombocytopenias with platelet counts less than 20 x 10(9) litre-1 and the homozygous forms of Bernard-Soulier syndrome and Glanzmann's thrombasthenia. The most frequently encountered mild haemostatic abnormalitie …
Comparable platelet disorders include the inherited thrombocytopenias with platelet counts less than 20 x 10(9) litre-1 and the homozygous f …
Lessons from rare maladies: leukocyte adhesion deficiency syndromes.
Harris ES, Weyrich AS, Zimmerman GA. Harris ES, et al. Curr Opin Hematol. 2013 Jan;20(1):16-25. doi: 10.1097/MOH.0b013e32835a0091. Curr Opin Hematol. 2013. PMID: 23207660 Free PMC article. Review.
Recent discoveries merit their review in the context of existing knowledge. RECENT FINDINGS: New activities of beta(2) integrins, which are deficient or absent in LAD-I, and new beta(2) integrin-dependent functions of neutrophils and other leukocytes have recently b …
Recent discoveries merit their review in the context of existing knowledge. RECENT FINDINGS: New activities of beta(2) integrins, whi …
Glanzmann's thrombasthenia.
Caen JP. Caen JP. Baillieres Clin Haematol. 1989 Jul;2(3):609-25. doi: 10.1016/s0950-3536(89)80036-8. Baillieres Clin Haematol. 1989. PMID: 2673430 Review. No abstract available.
Eptacog alfa activated: a recombinant product to treat rare congenital bleeding disorders.
Di Minno G. Di Minno G. Blood Rev. 2015 Jun;29 Suppl 1:S26-33. doi: 10.1016/S0268-960X(15)30005-9. Blood Rev. 2015. PMID: 26073366 Review.
Glanzmann's thrombasthenia (GT) and congenital factor VII deficiency (FVII CD) are rare autosomal recessive bleeding disorders: GT is the most frequent congenital platelet function disorder, and FVII CD is the most common factor-deficiency disease after haemophilia.
Glanzmann's thrombasthenia (GT) and congenital factor VII deficiency (FVII CD) are rare autosomal recessive bleeding disorders
51 results