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

Year Number of Results
1946 1
1949 3
1950 1
1951 3
1952 3
1953 2
1954 2
1955 2
1956 1
1957 1
1958 1
1959 1
1960 1
1961 6
1962 3
1963 7
1964 9
1965 8
1966 7
1967 7
1968 8
1969 5
1970 9
1971 9
1972 8
1973 4
1974 5
1975 12
1976 12
1977 9
1978 14
1979 14
1980 17
1981 21
1982 15
1983 19
1984 20
1985 32
1986 39
1987 34
1988 34
1989 27
1990 40
1991 33
1992 45
1993 40
1994 28
1995 34
1996 33
1997 38
1998 43
1999 25
2000 30
2001 29
2002 43
2003 46
2004 39
2005 37
2006 31
2007 35
2008 34
2009 43
2010 44
2011 34
2012 39
2013 34
2014 36
2015 42
2016 37
2017 39
2018 46
2019 38
2020 50
2021 41
2022 34
2023 45
2024 21

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1,635 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
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
Acquired Glanzmann thrombasthenia: From antibodies to anti-platelet drugs.
Nurden AT. Nurden AT. Blood Rev. 2019 Jul;36:10-22. doi: 10.1016/j.blre.2019.03.004. Epub 2019 Mar 20. Blood Rev. 2019. PMID: 31010659 Review.
In contrast to the inherited platelet disorder given by mutations in the ITGA2B and ITGB3 genes, mucocutaneous bleeding from a spontaneous inhibition of normally expressed alphaIIbbeta3 characterizes acquired Glanzmann thrombasthenia (GT). Classically, it is associa …
In contrast to the inherited platelet disorder given by mutations in the ITGA2B and ITGB3 genes, mucocutaneous bleeding from a spontaneous i …
Glanzmann's thrombasthenia: updated.
Nair S, Ghosh K, Kulkarni B, Shetty S, Mohanty D. Nair S, et al. Platelets. 2002 Nov;13(7):387-93. doi: 10.1080/0953710021000024394. Platelets. 2002. PMID: 12487785 Review.
Glanzmann's thrombasthenia is an autosomal recessive disorder, rare in a global context, but a relatively more common platelet function defect in communities where consanguineous marriages are more frequent. ...It has now been established that different genetic muta
Glanzmann's thrombasthenia is an autosomal recessive disorder, rare in a global context, but a relatively more common platelet
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
Glanzmann's thrombasthenia.
Tullu MS, Dixit PS, Nair SB, Kamat JR, Vaswani RK, Shetty SD, Pawar AR. Tullu MS, et al. Indian J Pediatr. 2001 Jun;68(6):563-6. doi: 10.1007/BF02723255. Indian J Pediatr. 2001. PMID: 11450390 Review.
Glanzmann's thrombasthenia (GT) is an uncommon cause of bleeding in children. ...
Glanzmann's thrombasthenia (GT) is an uncommon cause of bleeding in children. ...
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. ...
Glanzmann's thrombasthenia (GT) is an autosomal recessive inherited bleeding disorder due to a defect in platelet function. ..
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.
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders.
Fiore M, Giraudet JS, Alessi MC, Falaise C, Desprez D, d'Oiron R, Voisin S, Hurtaud MF, Boutroux H, Saultier P, Lavenu-Bombled C, Bagou G, Dubucs X, Chauvin A, Leroy C, Meckert F, Kerbaul F, Giraud N, Pühler A, Rath A. Fiore M, et al. Orphanet J Rare Dis. 2023 Jun 29;18(1):171. doi: 10.1186/s13023-023-02787-2. Orphanet J Rare Dis. 2023. PMID: 37386449 Free PMC article. Review.
Glanzmann thrombasthenia (GT) is a genetic bleeding disorder characterised by severely reduced/absent platelet aggregation in response to multiple physiological agonists. ...
Glanzmann thrombasthenia (GT) is a genetic bleeding disorder characterised by severely reduced/absent platelet aggregation in
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
1,635 results