203 related articles for article (PubMed ID: 27100304)
21. A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.
Lobo V; Shetty S; Kulkarni B; Butera D; Magalhaes GS; Ghosh K
Ann Hematol; 2012 Jun; 91(6):917-21. PubMed ID: 22183252
[TBL] [Abstract][Full Text] [Related]
22. Reliability and Feasibility of the Self-Administered ISTH-Bleeding Assessment Tool.
Punt MC; Blaauwgeers MW; Timmer MA; Welsing PMJ; Schutgens REG; van Galen KPM
TH Open; 2019 Oct; 3(4):e350-e355. PubMed ID: 31799494
[No Abstract] [Full Text] [Related]
23. Clinical phenotype in heterozygote and biallelic Bernard-Soulier syndrome--a case control study.
Bragadottir G; Birgisdottir ER; Gudmundsdottir BR; Hilmarsdottir B; Vidarsson B; Magnusson MK; Larsen OH; Sorensen B; Ingerslev J; Onundarson PT
Am J Hematol; 2015 Feb; 90(2):149-55. PubMed ID: 25370924
[TBL] [Abstract][Full Text] [Related]
24. Different biochemical expression pattern of platelet surface glycoproteins suggests molecular diversity of Glanzmann's thrombasthenia in Iran.
Farsinejad A; Farajollahi MM; Kazemi A; Saemi N; Faranoush M
Blood Coagul Fibrinolysis; 2013 Sep; 24(6):613-8. PubMed ID: 23912132
[TBL] [Abstract][Full Text] [Related]
25. Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease.
Clemetson KJ; Clemetson JM
Curr Opin Hematol; 1994 Sep; 1(5):388-93. PubMed ID: 9371310
[TBL] [Abstract][Full Text] [Related]
26. Glanzmann thrombasthenia and Bernard-Soulier syndrome in south Iran.
Afrasiabi A; Artoni A; Karimi M; Peyvandi F; Ashouri E; Mannucci PM
Clin Lab Haematol; 2005 Oct; 27(5):324-7. PubMed ID: 16178914
[TBL] [Abstract][Full Text] [Related]
27. Prospective evaluation of ISTH-BAT as a predictor of bleeding disorder in adolescents presenting with heavy menstrual bleeding in a multidisciplinary hematology clinic.
Jain S; Zhang S; Acosta M; Malone K; Kouides P; Zia A
J Thromb Haemost; 2020 Oct; 18(10):2542-2550. PubMed ID: 32654321
[TBL] [Abstract][Full Text] [Related]
28. Platelet receptors and functional disorders.
Clemetson KJ
Schweiz Med Wochenschr Suppl; 1991; 43():12-23. PubMed ID: 1668823
[No Abstract] [Full Text] [Related]
29. Survival and function of transfused platelets. Studies in two patients with congenital deficiencies of platelet membrane glycoproteins.
Cesar JM; Vecino AM
Platelets; 2009 May; 20(3):158-62. PubMed ID: 19437332
[TBL] [Abstract][Full Text] [Related]
30. Systematic analysis of bleeding phenotype in PT-VWD compared to type 2B VWD using an electronic bleeding questionnaire.
Kaur H; Ozelo M; Scovil S; James PD; Othman M
Clin Appl Thromb Hemost; 2014 Nov; 20(8):765-71. PubMed ID: 25063765
[TBL] [Abstract][Full Text] [Related]
31. Comprehensive Platelet Phenotypic Laboratory Testing and Bleeding History Scoring for Diagnosis of Suspected Hereditary Platelet Disorders: A Single-Institution Experience.
Perez Botero J; Warad DM; He R; Uhl CB; Tian S; Otteson GE; Barness RL; Olson MC; Gossman SC; Charlesworth JE; Nichols WL; Pruthi RK; Chen D
Am J Clin Pathol; 2017 Jul; 148(1):23-32. PubMed ID: 28575217
[TBL] [Abstract][Full Text] [Related]
32. The ISTH Bleeding Assessment Tool and the risk of future bleeding.
Fasulo MR; Biguzzi E; Abbattista M; Stufano F; Pagliari MT; Mancini I; Gorski MM; Cannavò A; Corgiolu M; Peyvandi F; Rosendaal FR
J Thromb Haemost; 2018 Jan; 16(1):125-130. PubMed ID: 29064634
[TBL] [Abstract][Full Text] [Related]
33. Congenital and acquired platelet disorders: current dilemmas and treatment strategies.
White GC
Semin Hematol; 2006 Jan; 43(1 Suppl 1):S37-41. PubMed ID: 16427384
[TBL] [Abstract][Full Text] [Related]
34. Responses of platelets to strains of streptococcus sanguis: findings in healthy subjects, Bernard-Soulier, Glanzmann's, and collagen-unresponsive patients.
Soberay AH; Herzberg MC; Rudney JD; Nieuwenhuis HK; Sixma JJ; Seligsohn U
Thromb Haemost; 1987 Apr; 57(2):222-5. PubMed ID: 3603413
[TBL] [Abstract][Full Text] [Related]
35. Normal range of bleeding scores for the ISTH-BAT: adult and pediatric data from the merging project.
Elbatarny M; Mollah S; Grabell J; Bae S; Deforest M; Tuttle A; Hopman W; Clark DS; Mauer AC; Bowman M; Riddel J; Christopherson PA; Montgomery RR; ; Rand ML; Coller B; James PD
Haemophilia; 2014 Nov; 20(6):831-5. PubMed ID: 25196510
[TBL] [Abstract][Full Text] [Related]
36. Elevated CD9 expression as a potential biomarker for diagnosis of Bernard-Soulier syndrome.
Sharifi MJ; Vakili E; Ilkhanipoor H; Zekavat OR; Bordbar M
Blood Coagul Fibrinolysis; 2022 Apr; 33(3):159-161. PubMed ID: 35165218
[TBL] [Abstract][Full Text] [Related]
37. Platelet prothrombin converting activity in hereditary disorders of platelet function.
Bevers EM; Comfurius P; Nieuwenhuis HK; Levy-Toledano S; Enouf J; Belluci S; Caen JP; Zwaal RF
Br J Haematol; 1986 Jun; 63(2):335-45. PubMed ID: 3718874
[TBL] [Abstract][Full Text] [Related]
38. Utility of the ISTH bleeding assessment tool in predicting platelet defects in participants with suspected inherited platelet function disorders.
Lowe GC; Lordkipanidzé M; Watson SP;
J Thromb Haemost; 2013 Sep; 11(9):1663-8. PubMed ID: 23809206
[TBL] [Abstract][Full Text] [Related]
39. Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the Bleeding Assesment Tool - LABoratory tests substudy): communication from the Platelet Physiology ISTH-SSC.
Gresele P; Falcinelli E; Bury L; Alessi MC; Guglielmini G; Falaise C; Podda G; Fiore M; Mazziotta F; Sevivas T; Bermejo N; De Candia E; Chitlur M; Lambert MP; Barcella L; Glembotsky AC; Lordkipanidzé M
Res Pract Thromb Haemost; 2024 Jan; 8(1):102305. PubMed ID: 38292347
[TBL] [Abstract][Full Text] [Related]
40. Clinical spectrum of Glanzmann's thrombasthenia.
Badhe BA; Jayanthi S; Datta T
Indian J Pathol Microbiol; 2000 Jul; 43(3):297-302. PubMed ID: 11218676
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
