83 results on '"Zaninetti, C"'
Search Results
2. PB0386 Increased Platelet Expression of the Transcriptional Suppressor ETV6 Can Be Detected by Immunofluorescence on the Blood Smear and Associates with ETV6-Related Thrombocytopenia
3. Platelet expression of the transcription factor ETV6 points toward ETV6-related thrombocytopenia and can be detected by immunofluorescence on the blood smear
4. A novel, homozygous mutation in GFI1B causing inherited thrombocytopenia with Glanzmann-like platelet dysfunction
5. Aggregates of non-muscle myosin IIA in the erythrocytes associate with GATA1-related thrombocytopenia
6. Platelet GPIIbIIIa enriched membrane protrusions (Tether) in healthy and diseased individuals
7. Assessment of platelet abnormalities in patients with DiGeorge Syndrome by immunofluorescence microscopy on the blood smear
8. Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
9. Extramedullary hematopoiesis: a new feature of inherited thrombocytopenias?
10. Bleeding is not the main clinical issue in many patients with inherited thrombocytopaenias
11. The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology
12. Platelets from patients with MYH9 related disorders are mechanically stiffer
13. Diagnosis of inherited platelet disorders: comparison between immunofluorescence analysis on the blood smear and genetic testing
14. Semiautomatic assessment of immunofluorescence microscopy on blood smears in inherited platelet disorders using artificial intelligence: a proof of concept.
15. Platelet phenotyping by immunofluorescence microscopy on the blood smears in patients with myeloproliferative neoplasms.
16. MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations
17. T-24-09: Aggregates of non-muscle myosin IIA in the erythrocytes associate with GATA1-related thrombocytopenia.
18. T-24-08: A novel, homozygous mutation in GFI1B causing inherited thrombocytopenia with Glanzmann-like platelet dysfunction.
19. T-24-07: Platelet expression of the transcription factor ETV6 points toward ETV6-related thrombocytopenia and can be detected by immunofluorescence on the blood smear.
20. T-24-04: Platelet GPIIbIIIa enriched membrane protrusions (Tether) in healthy and diseased individuals.
21. ACTA OTORHINOLARYNGOLOGICA ITALICA
22. Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia
23. T-24-06: Assessment of platelet abnormalities in patients with DiGeorge Syndrome by immunofluorescence microscopy on the blood smear.
24. Inherited thrombocytopenia caused by ANKRD26mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
25. Platelets from patients with MYH9 related disorders are mechanically stiffer.
26. Diagnosis of inherited platelet disorders: comparison between immunofluorescence analysis on the blood smear and genetic testing.
27. NOVEL PERSPECTIVES IN GENOTYPE-PHENOTYPE CORRELATIONS IN MYH9-RELATED DISEASE: NO LONGER JUST A MATTER OF HEAD OR TAIL
28. Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases
29. Disarrangement of Platelet Cytoskeleton might contribute to Hemorrhagic Diathesis in Scurvy.
30. Apoptosis and platelet biogenesis: A new piece of information on a debated topic.
31. Immunofluorescence microscopy on the blood smear identifies patients with myeloproliferative neoplasms.
32. Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.
33. Platelet expression of the transcription factor ETV6 associates with ETV6-related thrombocytopenia and can be detected by immunofluorescence on the blood film.
34. Rescue Therapy in Chronic Prothrombotic Autoimmune Anti-PF4 Disorder.
35. Platelet transcriptome analysis in patients with germline RUNX1 mutations.
36. Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders.
37. A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger.
38. Src-related thrombocytopenia: a fine line between a megakaryocyte dysfunction and an immune-mediated disease.
39. Reduced platelet forces underlie impaired hemostasis in mouse models of MYH9 -related disease.
40. Diagnosing Inherited Platelet Disorders: Modalities and Consequences.
41. The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark.
42. A novel homozygous GFI1B variant in 2 sisters with thrombocytopenia and severe bleeding tendency.
43. A flow cytometric assay to detect platelet-activating antibodies in VITT after ChAdOx1 nCov-19 vaccination.
44. Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients.
45. Spontaneous splenic rupture due to extramedullary haematopoiesis in a patient with inherited thrombocytopenia.
46. Anticoagulation in Patients with Platelet Disorders.
47. Role of Platelet Cytoskeleton in Platelet Biomechanics: Current and Emerging Methodologies and Their Potential Relevance for the Investigation of Inherited Platelet Disorders.
48. Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study.
49. Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial.
50. Diagnosis of Inherited Platelet Disorders on a Blood Smear.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.