Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim-Reference-Cited by-同舟云学术

Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim

Published:2017-11-30 Issue:1 Volume:10 Page:63-75
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Pecci Alessandro¹,Ragab Iman²,Bozzi Valeria¹,De Rocco Daniela³,Barozzi Serena¹,Giangregorio Tania⁴,Ali Heba²,Melazzini Federica¹,Sallam Mohamed⁵,Alfano Caterina⁶⁷,Pastore Annalisa⁸,Balduini Carlo L¹,Savoia Anna³⁴^ORCID

Affiliation:

1. Department of Internal Medicine IRCCS Policlinico San Matteo Foundation and University of Pavia Pavia Italy

2. Hematology‐Oncology Unit Pediatric Hospital Ain Shams University Cairo Egypt

3. Institute for Maternal and Child Health – IRCCS Burlo Garofolo Trieste Italy

4. Department of Medical Sciences University of Trieste Trieste Italy

5. Department of Clinical Pathology Ain Shams University Cairo Egypt

6. Maurice Wohl Clinical Neuroscience Institute King's College London UK

7. Fondazione Ri.MED Palermo Italy

8. Department of Molecular Medicine University of Pavia Pavia Italy

Funder

Fondazione Cariplo

Ministero della Salute

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201708168

Reference27 articles.

1. c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

2. Thrombopoietin Is Essential for the Maintenance of Normal Hematopoiesis in Humans

3. Advances in the understanding of congenital amegakaryocytic thrombocytopenia

4. Congenital Amegakaryocytic Thrombocytopenia: Clinical Presentation, Diagnosis, and Treatment

5. Flow cytometric detection of MPL (CD110) as a diagnostic tool for differentiation of congenital thrombocytopenias

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