How we(’ll) treat paroxysmal nocturnal haemoglobinuria: diving into the future-Reference-Cited by-同舟云学术

How we(’ll) treat paroxysmal nocturnal haemoglobinuria: diving into the future

Published:2021-08-05 Issue:2 Volume:196 Page:288-303
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Risitano Antonio Maria¹²³^ORCID,Peffault de Latour Régis³⁴⁵

Affiliation:

1. Department of Onco‐Hematology AORN San Giuseppe Moscati Avellino Avellino Italy

2. Department of Clinical Medicine and Surgery Federico II University of Naples Naples Italy

3. Severe Aplastic Anaemia Working Party (SAAWP) of the European Group for Bone Marrow Transplantation (EBMT) Leiden the Netherlands

4. French Reference Centre for Aplastic Anaemia and Paroxysmal Nocturnal Haemoglobinuria Assistance Publique – Hôpitaux de Paris Saint‐Louis Hospital Paris France

5. Bone Marrow Transplant Unit Université de Paris, Denis Diderot Paris France

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17753

Reference96 articles.

1. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

2. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene.

3. Abnormalities of PIG-A Transcripts in Granulocytes from Patients with Paroxysmal Nocturnal Hemoglobinuria

4. 7 Paroxysmal nocturnal haemoglobinuria

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