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1.
Pathogenic mechanisms contributing to thrombocytopenia in patients with systemic lupus erythematosus.
Platelets
; 33(5): 743-754, 2022 Jul 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34806522
2.
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study.
Haematologica
; 105(7): 1948-1956, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31558677
3.
Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.
Haematologica
; 104(6): 1244-1255, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30545930
4.
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders.
Haematologica
; 102(7): 1192-1203, 2017 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-28385783
5.
Differential expression of SDF-1 receptor CXCR4 in molecularly defined forms of inherited thrombocytopenias.
Platelets
; 28(6): 602-606, 2017 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-28032520
6.
Long-term follow-up of essential thrombocythemia patients treated with anagrelide: subgroup analysis according to JAK2/CALR/MPL mutational status.
Eur J Haematol
; 96(4): 435-42, 2016 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-26119186
7.
First description of revertant mosaicism in familial platelet disorder with predisposition to acute myelogenous leukemia: correlation with the clinical phenotype.
Haematologica
; 105(10): e535, 2020 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33054100
8.
Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome.
Platelets
; 26(8): 751-7, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25806575
9.
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
Hum Mutat
; 35(2): 236-47, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24186861
10.
Impaired proplatelet formation in immune thrombocytopenia: a novel mechanism contributing to decreased platelet count.
Br J Haematol
; 165(6): 854-64, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24673454
11.
Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression.
Blood
; 120(13): 2708-18, 2012 Sep 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-22898599
12.
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.
Haematologica
; 99(8): 1387-94, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24763399
13.
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.
Res Pract Thromb Haemost
; 8(1): 102305, 2024 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-38292347
14.
Toll-like receptor expression and functional behavior in platelets from patients with systemic lupus erythematosus.
Immunobiology
; 229(1): 152782, 2024 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-38159527
15.
Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency.
Haematologica
; 98(6): 868-74, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23100277
16.
High cell-free DNA is associated with disease progression, inflammasome activation and elevated levels of inflammasome-related cytokine IL-18 in patients with myelofibrosis.
Front Immunol
; 14: 1161832, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38035089
17.
Mutations of RUNX1 in families with inherited thrombocytopenia.
Am J Hematol
; 92(6): E86-E88, 2017 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-28240786
18.
Gray platelet syndrome: Novel mutations of the NBEAL2 gene.
Am J Hematol
; 92(2): E20-E22, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27870194
19.
A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation.
J Blood Med
; 12: 719-732, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34408521
20.
Screening for MPL mutations in essential thrombocythemia and primary myelofibrosis: normal Mpl expression and absence of constitutive STAT3 and STAT5 activation in MPLW515L-positive platelets.
Eur J Haematol
; 84(5): 398-405, 2010 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-20113333