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Quoted phrase not found in phrase index: "Glanzmann thrombasthenia 2"
Page 1
Clinical and molecular insights into Glanzmann's thrombasthenia in China.
Zhou L, Jiang M, Shen H, You T, Ding Z, Cui Q, Ma Z, Yang F, Xie Z, Shi H, Su J, Cao L, Lin J, Yin J, Dai L, Wang H, Wang Z, Yu Z, Ruan C, Xia L. Zhou L, et al. Clin Genet. 2018 Aug;94(2):213-220. doi: 10.1111/cge.13366. Epub 2018 May 22. Clin Genet. 2018. PMID: 29675921 Free PMC article.
Glanzmann's thrombasthenia (GT) is a rare bleeding disorder characterized by spontaneous mucocutaneous bleeding. ...Han females suffered more severe bleeding and had a poorer prognosis. We identified a total of 43 different ITGA2B and ITGB3 variants, includin …
Glanzmann's thrombasthenia (GT) is a rare bleeding disorder characterized by spontaneous mucocutaneous bleeding. ...Han female …
Indication for allogeneic stem cell transplantation in Glanzmann's thrombasthenia.
Wiegering V, Sauer K, Winkler B, Eyrich M, Schlegel PG. Wiegering V, et al. Hamostaseologie. 2013;33(4):305-12. doi: 10.5482/HAMO-12-08-0014. Epub 2013 Jul 18. Hamostaseologie. 2013. PMID: 23868573 Review.
Glanzmann's thrombasthenia (GT) is an autosomal recessive disorder characterized by a lack of thrombocyte aggregation due to the absence of thrombocyte glycoproteins IIb and alphaIIbbeta3. ...
Glanzmann's thrombasthenia (GT) is an autosomal recessive disorder characterized by a lack of thrombocyte aggregation due to t …
Glanzmann Thrombasthenia: A Clinicopathological Profile.
Iqbal I, Farhan S, Ahmed N. Iqbal I, et al. J Coll Physicians Surg Pak. 2016 Aug;26(8):647-50. J Coll Physicians Surg Pak. 2016. PMID: 27539755
OBJECTIVE: To describe the clinical presentation of patients with Glanzmann's thrombasthenia (GT) and evaluate their diagnostic, clinical, and laboratory parameters including platelet aggregometry. ...Platelet aggregation studies showed decreased aggregation with AD …
OBJECTIVE: To describe the clinical presentation of patients with Glanzmann's thrombasthenia (GT) and evaluate their diagnosti …
A microchip flow-chamber assay screens congenital primary hemostasis disorders.
Nakajima Y, Yada K, Ogiwara K, Furukawa S, Shimonishi N, Shima M, Nogami K. Nakajima Y, et al. Pediatr Int. 2021 Feb;63(2):160-167. doi: 10.1111/ped.14378. Epub 2020 Dec 5. Pediatr Int. 2021. PMID: 32640065
We report the usefulness of a microchip flow-chamber system (T-TAS() ) for detecting and/or predicting clinical severity in patients with VWD type 1 and type 2N and platelet storage pool disease. ...METHODS: Microchips coated with collagen (PL-chip) and collagen/thrombopla …
We report the usefulness of a microchip flow-chamber system (T-TAS() ) for detecting and/or predicting clinical severity in patients …
High-throughput elucidation of thrombus formation reveals sources of platelet function variability.
van Geffen JP, Brouns SLN, Batista J, McKinney H, Kempster C, Nagy M, Sivapalaratnam S, Baaten CCFMJ, Bourry N, Frontini M, Jurk K, Krause M, Pillitteri D, Swieringa F, Verdoold R, Cavill R, Kuijpers MJE, Ouwehand WH, Downes K, Heemskerk JWM. van Geffen JP, et al. Haematologica. 2019 Jun;104(6):1256-1267. doi: 10.3324/haematol.2018.198853. Epub 2018 Dec 13. Haematologica. 2019. PMID: 30545925 Free PMC article.
Principal component analyses indicated coherence between the majority of parameters for the GPVI-dependent microspots, partly linked to hematologic parameters, and glycoprotein expression levels. Prediction models identified parameters per microspot that were linked to var …
Principal component analyses indicated coherence between the majority of parameters for the GPVI-dependent microspots, partly linked to hema …
The necessity of repeat testing for von Willebrand disease in adult patients with mild to moderate bleeding disorders.
Mehic D, Kraemmer D, Tolios A, Bücheler J, Quehenberger P, Haslacher H, Ay C, Pabinger I, Gebhart J. Mehic D, et al. J Thromb Haemost. 2024 Jan;22(1):101-111. doi: 10.1016/j.jtha.2023.09.010. Epub 2023 Sep 21. J Thromb Haemost. 2024. PMID: 37741511
Using logistic regression, we estimated a probability of change of 26.4% (95% CI, 12.5-47.4) at baseline VWF levels of 30 IU/dL, 50.8% (95% CI, 35.6-65.8) at 50 IU/dL, 18.8% (95% CI, 12.3-27.6) at 60 IU/dL, and 1.2% (95% CI, 0.3-4.9) at 80 IU/dL. Baseline VWF was a strong pred …
Using logistic regression, we estimated a probability of change of 26.4% (95% CI, 12.5-47.4) at baseline VWF levels of 30 IU/dL, 50.8% (95% …
Late postoperative hemorrhage in a patient with undiagnosed COX-1 deficiency after third molar extractions.
Doscher JC, Volpe FN. Doscher JC, et al. J Oral Maxillofac Surg. 2014 Apr;72(4):660-5. doi: 10.1016/j.joms.2013.11.013. Epub 2013 Nov 22. J Oral Maxillofac Surg. 2014. PMID: 24480756 Review.
Platelets have 3 distinct roles in coagulation: initial adhesion, phospholipid externalization, and platelet aggregation.(1) Several types of platelet deficiencies, including defects of adhesion (Bernard-Soulier syndrome), defects of aggregation (Glanzmann thrombastheni …
Platelets have 3 distinct roles in coagulation: initial adhesion, phospholipid externalization, and platelet aggregation.(1) Several types o …
Successful Use of Hematopoietic Stem Cell Transplantation for 2 Pediatric Cases of Glanzmann Thrombasthenia and Review of the Literature.
Friend BD, Roach GD, Kempert PH, Moore TB. Friend BD, et al. J Pediatr Hematol Oncol. 2020 Aug;42(6):e521-e526. doi: 10.1097/MPH.0000000000001646. J Pediatr Hematol Oncol. 2020. PMID: 31693514 Review.
Glanzmann thrombasthenia is a rare platelet disorder characterized by an abnormal integrin receptor on the surface of platelets that results in the failure of platelets to aggregate. Currently, curative therapy is allogeneic hematopoietic stem cell transplantation ( …
Glanzmann thrombasthenia is a rare platelet disorder characterized by an abnormal integrin receptor on the surface of platelet …
A Glanzmann thrombasthenia family associated with a TUBB1-related macrothrombocytopenia.
Guillet B, Bayart S, Pillois X, Nurden P, Caen JP, Nurden AT. Guillet B, et al. J Thromb Haemost. 2019 Dec;17(12):2211-2215. doi: 10.1111/jth.14622. Epub 2019 Sep 29. J Thromb Haemost. 2019. PMID: 31565851 Free article.
BACKGROUND: Macrothrombocytopenia (MTP) is a rare but enigmatic complication of Glanzmann thrombasthenia (GT), an inherited bleeding disorder caused by the absence of platelet aggregation due to deficiencies of the alphaIIbbeta3 integrin. ...METHODS AND RESULTS: San …
BACKGROUND: Macrothrombocytopenia (MTP) is a rare but enigmatic complication of Glanzmann thrombasthenia (GT), an inherited bl …
A Novel Frameshift Mutation in the ITGB3 Gene Leading to Glanzmann's Thrombasthenia in a Saudi Arabian Family.
Alharbi A, Hashmi JA, Alharby E, Albalawi AM, Ramzan K, Basit S. Alharbi A, et al. Hematol Oncol Stem Cell Ther. 2022 Mar 1;15(1):21-26. doi: 10.1016/j.hemonc.2021.01.003. Hematol Oncol Stem Cell Ther. 2022. PMID: 33600779
Glanzmann's thrombasthenia (GT) is an autosomal recessive congenital bleeding disorder of platelet aggregation. ...The single nucleotide deletion variant (c.2113delC) in exon 13 of the ITGB3 gene is predicted to cause a frameshift and absence of vital C-termi …
Glanzmann's thrombasthenia (GT) is an autosomal recessive congenital bleeding disorder of platelet aggregation. ...The single …
41 results