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8 in total

1. Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B.

Authors: Carlos R Ferreira; Dong Chen; Shirley M Abraham; David R Adams; Karen L Simon; May C Malicdan; Thomas C Markello; Meral Gunay-Aygun; William A Gahl
Journal: Mol Genet Metab Date: 2016-12-18 Impact factor: 4.797

Review 2. Platelet disorders: a review of disturbances in adhesion, aggregation, and release reaction.

Authors: M A Sahud
Journal: Calif Med Date: 1972-01

Review 3. Hematopoietic transcription factor mutations: important players in inherited platelet defects.

Authors: Natthapol Songdej; A Koneti Rao
Journal: Blood Date: 2017-04-17 Impact factor: 22.113

Review 4. Inherited platelet dysfunction and hematopoietic transcription factor mutations.

Authors: Natthapol Songdej; A Koneti Rao
Journal: Platelets Date: 2016-07-27 Impact factor: 3.862

5. Gray platelet syndrome: selective alpha-granule deficiency and thrombocytopenia due to increased platelet turnover.

Authors: M Köhler; P Hellstern; E Morgenstern; C Mueller-Eckhardt; R Berberich; R J Meiser; P Scheffler; E Wenzel
Journal: Blut Date: 1985-06

6. Hereditary giant platelet syndrome: a disorder of a new aspect of platelet function.

Authors: M A Howard; R A Hutton; R M Hardisty
Journal: Br Med J Date: 1973-06-09

Review 7. Hematopoietic transcription factor mutations and inherited platelet dysfunction.

Authors: Natthapol Songdej; A Koneti Rao
Journal: F1000Prime Rep Date: 2015-05-26

8. Dominant negative Gfi1b mutations cause moderate thrombocytopenia and an impaired stress thrombopoiesis associated with mild erythropoietic abnormalities in mice.

Authors: Hugues Beauchemin; Peiman Shooshtharizadeh; Jordan Pinder; Graham Dellaire; Tarik Möröy
Journal: Haematologica Date: 2020-10-01 Impact factor: 9.941

8 in total