Natural history of Ras‐associated autoimmune leukoproliferative disorder: A 20‐year follow‐up of a <scp><i>NRAS</i></scp>‐mutated patient excluding a malignant progression-Reference-Cited by-同舟云学术

Natural history of Ras‐associated autoimmune leukoproliferative disorder: A 20‐year follow‐up of a NRAS‐mutated patient excluding a malignant progression

Published:2023-11-03 Issue:1 Volume:204 Page:
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Rivalta B.¹²,Attardi E.²³^ORCID,Cifaldi C.¹,Rosti V.⁴^ORCID,Pacillo L.¹²,Hajrullaj H.²³,Di Cesare S.¹⁵,Amodio D.¹⁵,Algeri M.⁶,Luciani M.⁶,Barzaghi F.⁷,Finocchi A.¹⁵,Di Matteo G.¹⁵,Aiuti A.⁷⁸,Locatelli F.⁶⁹^ORCID,Voso M. T.³^ORCID,Palumbo G.⁵⁶,Cancrini C.¹⁵

Affiliation:

1. Research Unit of Primary Immunodeficiencies, Academic Department of Pediatrics Bambino Gesù Children's Hospital, Scientific Institute for Research and Healthcare (IRCCS) Rome Italy

2. PhD Program in Immunology, Molecular Medicine and Applied Biotechnology University of Rome Tor Vergata Rome Italy

3. Department of Biomedicine and Prevention University of Rome Tor Vergata Rome Italy

4. Center for the Study of Myelofibrosis IRCCS Policlinico San Matteo Foundation Pavia Italy

5. Department of Systems Medicine University of Rome Tor Vergata Rome Italy

6. Department of Pediatric Hemato‐Oncology and Cell and Gene Therapy Bambino Gesù Children's Hospital, Scientific Institute for Research and Healthcare (IRCCS) Rome Italy

7. Pediatric Immunohematology and Bone Marrow Transplantation Unit IRCCS San Raffaele Scientific Institute Milan Italy

8. San Raffaele Telethon Institute for Gene Therapy (SR‐Tiget) IRCCS San Raffaele Scientific Institute Milan Italy

9. Department of Life Sciences and Public Health Catholic University of the Sacred Heart Rome Italy

Funder

Ministero della Salute

Ospedale Pediatrico Bambino Gesù

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.19150

Reference15 articles.

1. Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

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