Efficacy of romiplostim in treatment of thrombocytopenia in children with Wiskott–Aldrich syndrome-Reference-Cited by-同舟云学术

Efficacy of romiplostim in treatment of thrombocytopenia in children with Wiskott–Aldrich syndrome

Published:2020-10-31 Issue:2 Volume:192 Page:366-374
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Khoreva Anna¹^ORCID,Abramova Irina¹^ORCID,Deripapa Elena¹^ORCID,Rodina Yulia¹^ORCID,Roppelt Anna¹^ORCID,Pershin Dmitry²^ORCID,Larin Sergey³^ORCID,Voronin Kirill⁴^ORCID,Maschan Alexey⁵^ORCID,Novichkova Galina⁶^ORCID,Shcherbina Anna¹^ORCID

Affiliation:

1. Department of Immunology Dmitry Rogachev National Medical Center of Pediatric Hematology, Oncology and Immunology Moscow Russia

2. Laboratory of Hematopoietic Stem Cell Transplantation and Immunotherapy Dmitry Rogachev National Medical Center of Pediatric Hematology, Oncology and Immunology Moscow Russia

3. Laboratory of Molecular Immunology Dmitry Rogachev National Medical Center of Pediatric Hematology, Oncology and Immunology Moscow Russia

4. Department of Bioinformatics and Medical Statistics Dmitry Rogachev National Medical Center of Pediatric Hematology, Oncology and Immunology Moscow Russia

5. Department of Hematopoietic Stem Cell Transplantation Dmitry Rogachev National Medical Center of Pediatric Hematology, Oncology and Immunology Moscow Russia

6. Department of Pediatric Hematology and Oncology Dmitry Rogachev National Medical Center of Pediatric Hematology, Oncology and Immunology Moscow Russia

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17174

Reference48 articles.

1. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

2. Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome

3. X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options

4. A multiinstitutional survey of the Wiskott-Aldrich syndrome

5. Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study

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