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Journal Articles

Pediatric hemophagocytic lymphohistiocytosis

Scott W. Canna, Rebecca A. Marsh

Blood (2020) 135 (16): 1332–1343.

https://doi.org/10.1182/blood.2019000936

Published: 2020

Journal Articles

Clonal T-Large Granular Lymphocyte Proliferations in Childhood: Friend or Foe?

Sureyya Savasan, MD, Batool Al-Qanber, MD, Steven Buck, MS, Erin Wakeling, PhD, Manisha Gadgeel, MBBS, MS

Blood (2018) 132 (Supplement 1): 3719.

https://doi.org/10.1182/blood-2018-99-119124

Published: 2018

Journal Articles

Adaptive reprogramming of NK cells in X-linked lymphoproliferative syndrome

Stephen Opat, Anna C. Hearps, Kevin Thia, Agnes Yuen, Ben Rogers, Mkunde Chachage, Gregory Moore, Jake Shortt, Georgina Ryland, Piers Blombery, Anthony P. Schwarer, Tahereh Noori, Joseph A. Trapani, Anthony Jaworowski, Ilia Voskoboinik

Blood (2018) 131 (6): 699–702.

https://doi.org/10.1182/blood-2017-08-803668

Published: 2018

Includes: Supplemental data

Journal Articles

Allogeneic Stem Cell Transplantation for the Treatment of Lymphoproliferative Disorders in Patients Affected By Primary Immunodeficiencies: The UK Experience

Giulia Prunotto, Giovanna Lucchini, MD, Sujith Samarasinghe, Robert Wynn, MD, Ajay Vora, MD, Ben Carpenter, Claire Gowdy, Kieran Mchugh, Andrew Gennery, MD, Paul Veys, MD PhD, Christopher Bacon, Simon Bomken

Blood (2017) 130 (Supplement 1): 4573.

https://doi.org/10.1182/blood.V130.Suppl_1.4573.4573

Published: 2017

Journal Articles

Hematopoietic Stem Cell Transplantation for Hemophagocytic Lymphohistiocitosis : A National Retrospective Analysis of Data from the Italian Association of Pediatric Hematology Oncology (AIEOP)

Blood (2015) 126 (23): 621.

https://doi.org/10.1182/blood.V126.23.621.621

Published: 2015

Journal Articles

Hemophagocytic Lymphohistiocytosis Associated with NK Cell Dysfunction and Disseminated Herpesvirus Infection in GATA2 Deficiency/Monomac Syndrome

Michael A. Spinner, MD, Camila Odio, B.S., Katherine R. Calvo, MD, PhD, Amy P Hsu, B.A., Christa S. Zerbe, MD, Jennifer Cuellar-Rodriguez, MD, Jennifer P. Ker, MD, Charles J. Stoudenmire, MD, Oluwole Fadare, MD, Arunima Ghosh, MD,PhD, Emily M. Mace, PhD, Jordan S. Orange, MD, PhD, Dennis D. Hickstein, MD, Steven M. Holland, MD

Blood (2014) 124 (21): 4978.

https://doi.org/10.1182/blood.V124.21.4978.4978

Published: 2014

Journal Articles

A Mouse Model for XLP-2 Disease Uncovers a Critical Function for IL-1beta and TNF in Driving Hyper-Inflammation

Philipp J. Jost, MD, Monica Yabal, PhD, Heiko Adler, PhD, Nathalie Knies, Christina Groß, Rune Busk Damgaard, Hirokazu Kanegane, MD PhD, Christian Peschel, MD, Andreas Strasser, PhD, Olaf Groß, Jürgen Ruland, MD, Mads Gyrd-Hansen, PhD

Blood (2014) 124 (21): 1403.

https://doi.org/10.1182/blood.V124.21.1403.1403

Published: 2014

Journal Articles

Robust Immune Reconstitution in Children with Severe Primary Immunodeficiency after Reduced-Intensity Conditioning Hematopoietic Stem Cell Transplantation

William T. Tse, MD PhD, Jessica Ward, MSN, cPNP, Jennifer Schneiderman, MD MS, Sonali Chaudhury, MD, Ramsay Fuleihan, MD, Reggie Duerst, MD, Morris Kletzel, MD

Blood (2014) 124 (21): 3923.

https://doi.org/10.1182/blood.V124.21.3923.3923

Published: 2014

Journal Articles

SAP gene transfer restores cellular and humoral immune function in a murine model of X-linked lymphoproliferative disease

Christine Rivat, Claire Booth, Maria Alonso-Ferrero, Michael Blundell, Neil J. Sebire, Adrian J. Thrasher, H. Bobby Gaspar

Blood (2013) 121 (7): 1073–1076.

https://doi.org/10.1182/blood-2012-07-445858

Published: 2013

Includes: Supplemental data

Journal Articles

Occurence of Malignancies in Patients with Primary Immunodeficiencies: An Analysis of the French Primary Immunodeficency Registry

Felipe Suarez, MD, PhD, Hugo Chapdelaine, M.D., Laetitia Compain, Nizar Mahlaoui, MD, Chantal Andriamanga, M.D, Alain Fischer, Olivier Hermine, MD, PhD

Blood (2012) 120 (21): 1057.

https://doi.org/10.1182/blood.V120.21.1057.1057

Published: 2012

Journal Articles

Hemophagocytic Lymphohistiocytosis: Update of Biology and Treatment Options

Alexandra H. Filipovich, MD

Blood (2012) 120 (21): SCI-9.

https://doi.org/10.1182/blood.V120.21.SCI-9.SCI-9

Published: 2012

Journal Articles

Booth C, Gilmour KC, Veys P, et al. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. Blood . 2011;117(1): 53–62 .

Blood (2011) 118 (18): 5060.

https://doi.org/10.1182/blood-2011-09-377911

Published: 2011

Journal Articles

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

Blood (2011) 117 (5): 1522–1529.

https://doi.org/10.1182/blood-2010-07-298372

Published: 2011

Includes: Supplemental data

Journal Articles

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

Blood (2011) 117 (1): 53–62.

https://doi.org/10.1182/blood-2010-06-284935

Published: 2011

Includes: Supplemental data

Journal Articles

X-linked lymphoproliferative syndromes: brothers or distant cousins?

Alexandra H. Filipovich, Kejian Zhang, Andrew L. Snow, Rebecca A. Marsh

Blood (2010) 116 (18): 3398–3408.

https://doi.org/10.1182/blood-2010-03-275909

Published: 2010

Journal Articles

To B or not to B

Kristina T. Lu, Pamela L. Schwartzberg

Blood (2010) 116 (17): 3120–3121.

https://doi.org/10.1182/blood-2010-08-299222

Published: 2010

Journal Articles

Impaired Epstein-Barr virus–specific CD8 + T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family–positive B-cell targets

Andrew D. Hislop, Umaimainthan Palendira, Alison M. Leese, Peter D. Arkwright, Pierre S. Rohrlich, Stuart G. Tangye, H. Bobby Gaspar, Arjan C. Lankester, Alessandro Moretta, Alan B. Rickinson

Blood (2010) 116 (17): 3249–3257.

https://doi.org/10.1182/blood-2009-09-238832

Published: 2010

Includes: Supplemental data

Journal Articles

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

Rebecca A. Marsh, Lisa Madden, Brenda J. Kitchen, Rajen Mody, Brad McClimon, Michael B. Jordan, Jack J. Bleesing, Kejian Zhang, Alexandra H. Filipovich

Blood (2010) 116 (7): 1079–1082.

https://doi.org/10.1182/blood-2010-01-256099

Published: 2010

Includes: Supplemental data

Journal Articles

A Study of Immune Deficiency as Risk Factor of Hodgkin's Lymphoma in Children.

Leila Hamdi, Rita Creidy, Jr., Patricia Rince, Karim Abbed, Jacqueline Clavel, Martine Raphael, Sr., Judith Landman-Parker, Caroline Besson, MD

Blood (2009) 114 (22): 1559.

https://doi.org/10.1182/blood.V114.22.1559.1559

Published: 2009

Journal Articles

Epstein-Barr virus persistence in the absence of conventional memory B cells: IgM + IgD + CD27 + B cells harbor the virus in X-linked lymphoproliferative disease patients

Sridhar Chaganti, Cindy S. Ma, Andrew I. Bell, Debbie Croom-Carter, Andrew D. Hislop, Stuart G. Tangye, Alan B. Rickinson

Blood (2008) 112 (3): 672–679.

https://doi.org/10.1182/blood-2007-10-116269

Published: 2008

NARROW

Pediatric hemophagocytic lymphohistiocytosis

Clonal T-Large Granular Lymphocyte Proliferations in Childhood: Friend or Foe?

Adaptive reprogramming of NK cells in X-linked lymphoproliferative syndrome

Allogeneic Stem Cell Transplantation for the Treatment of Lymphoproliferative Disorders in Patients Affected By Primary Immunodeficiencies: The UK Experience

Hematopoietic Stem Cell Transplantation for Hemophagocytic Lymphohistiocitosis : A National Retrospective Analysis of Data from the Italian Association of Pediatric Hematology Oncology (AIEOP)

Hemophagocytic Lymphohistiocytosis Associated with NK Cell Dysfunction and Disseminated Herpesvirus Infection in GATA2 Deficiency/Monomac Syndrome

A Mouse Model for XLP-2 Disease Uncovers a Critical Function for IL-1beta and TNF in Driving Hyper-Inflammation

Robust Immune Reconstitution in Children with Severe Primary Immunodeficiency after Reduced-Intensity Conditioning Hematopoietic Stem Cell Transplantation

SAP gene transfer restores cellular and humoral immune function in a murine model of X-linked lymphoproliferative disease

Occurence of Malignancies in Patients with Primary Immunodeficiencies: An Analysis of the French Primary Immunodeficency Registry

Hemophagocytic Lymphohistiocytosis: Update of Biology and Treatment Options

Booth C, Gilmour KC, Veys P, et al. X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease. Blood . 2011;117(1): 53–62 .

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

X-linked lymphoproliferative syndromes: brothers or distant cousins?

To B or not to B

Impaired Epstein-Barr virus–specific CD8 + T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family–positive B-cell targets

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

A Study of Immune Deficiency as Risk Factor of Hodgkin's Lymphoma in Children.

Epstein-Barr virus persistence in the absence of conventional memory B cells: IgM + IgD + CD27 + B cells harbor the virus in X-linked lymphoproliferative disease patients

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American Society of Hematology

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