Successful engraftment and stable full donor chimerism after myeloablation with thiotepa, fludarabine, and melphalan and CD34-selected peripheral allogeneic stem cell transplantation in hemophagocytic lymphohistiocytosis-Reference-Cited by-同舟云学术

Successful engraftment and stable full donor chimerism after myeloablation with thiotepa, fludarabine, and melphalan and CD34-selected peripheral allogeneic stem cell transplantation in hemophagocytic lymphohistiocytosis

Published:2003-01-28 Issue:2 Volume:72 Page:143-146
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Cesaro Simone,Gazzola Maria Vittoria,Marson Piero,Calore Elisabetta,Caenazzo Luciana,Destro Roberta,De Silvestro Giustina,Varotto Stefania,Pillon Marta,Zanesco Luigi,Messina Chiara

Publisher

Wiley

Subject

Hematology

Reference16 articles.

1. Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping

2. Linkage of Familial Hemophagocytic Lymphohistiocytosis to 10q21-22 and Evidence for Heterogeneity

3. Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis

4. HLH-94: A treatment protocol for hemophagocytic lymphohistiocytosis

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1. Spectrum of imaging appearances in Australian children with central nervous system hemophagocytic lymphohistiocytosis;Journal of Clinical Neuroscience;2014-02

2. Haploidentical allogeneic hematopoietic cell transplantation in adults using CD3/CD19 depletion and reduced intensity conditioning: a phase II study;Haematologica;2012-04-04

3. Familial hemophagocytic lymphohistiocytosis: clinical and neuroradiological findings and review of the literature;Child's Nervous System;2009-08-01

4. Hematopoietic stem cell transplantation for hemophagocytic lymphohistiocytosis: a retrospective analysis of data from the Italian Association of Pediatric Hematology Oncology (AIEOP);Haematologica;2008-09-11

5. FATAL SIBLING CASES OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (FHL) WITH MUNC13–4 MUTATIONS: Case Reports;Pediatric Hematology and Oncology;2008-01