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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

Genetic of Sporadic Hemophagocytic Lymphohistiocytosis

Coralie Bloch, MD PhD, Jean-Philippe Jais, MD PhD, Marine Gil, Marouane Boubaya, PhD, Felipe Suarez, MD PhD, Brigitte Bader-Meunier, MD, Nizar Malhaoui, MD PhD, Alain Fischer, MD PhD, Genevieve de Saint Basile, MD PhD, Olivier Hermine, MD PhD

Blood (2019) 134 (Supplement_1): 82.

https://doi.org/10.1182/blood-2019-129743

Published: 2019

Journal Articles

Novel Immune Checkpoint Deficiency and Susceptibility to EBV-Associated Lymphoma

Ido Somekh, Thomas Magg, PhD, Alejandro Gallón Duque, Tali Stauber, MD, Atar Lev, MSc, Ekrem Unal, MD, Amos J. Simon, PhD, Meino Rohlfs, PhD, Raffaele Conca, MSc, Megumi Tatematsu, PhD, Fabian Hauck, MD PhD, Raz Somech, MD PhD, Christoph Klein, MD PhD

Blood (2019) 134 (Supplement_1): 2326.

https://doi.org/10.1182/blood-2019-128296

Published: 2019

Journal Articles

Manufacture of Clinical-Grade Universal Antigen Presenting Cells (UAPC) for the Ex Vivo Expansion and Activation of Natural Killer (NK) Cells

Enli Liu, MD, Sonny Ang, PhD, Yijiu Tong, Li Li, MD, Rafet Basar, MD, Lucila Kerbauy, MD, May Daher, Pinaki P Banerjee, PhD, Francesca Lorraine Wei Inng Lim, MD, Indreshpal Kaur, PhD, Richard E Champlin, MD, Elizabeth J. Shpall, MD, Katy Rezvani, MD PhD

Blood (2018) 132 (Supplement 1): 2061.

https://doi.org/10.1182/blood-2018-99-118804

Published: 2018

Journal Articles

Retrospective Next Generation DNA Sequencing Analysis in Patients with Hemophagocytic Lymphohistiocytosis (HLH) Highlights Genetic Variants Associated with Secondary/Late-Onset Disease

Meeta Sunil, Chirantan Bose, Coral Karunakaran, Sunil Bhat, MBBS, MD, Nita Radhakrishnan, Srisha Rani, Sakthivel Murugan SM, Sharat Damodar, MBBS, MD DM, Ravi Gupta, Rohit Gupta, Mukesh Manharlal Desai, MBBS,MD, Arati Khanna-Gupta, PhD

Blood (2017) 130 (Supplement 1): 2286.

https://doi.org/10.1182/blood.V130.Suppl_1.2286.2286

Published: 2017

Journal Articles

Genetic Defects Affecting Lymphocyte Cytotoxicity in Epstein-Barr Virus-Associated T/NK-Cell Lymphoproliferative Diseases

Wei Zhang, MD, Xiao Min, MD PhD, Zhou Jianfeng, MD PhD

Blood (2017) 130 (Supplement 1): 4002.

https://doi.org/10.1182/blood.V130.Suppl_1.4002.4002

Published: 2017

Journal Articles

L-DEP Is an Effective Treatment for Adult and Adolescent Patients with Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis

Wenyuan Lai, Yini Wang, PhD, Jingshi Wang, Zhao Wang, MD

Blood (2016) 128 (22): 2521.

https://doi.org/10.1182/blood.V128.22.2521.2521

Published: 2016

Journal Articles

Pedigree Gene Investigation and Parameters of NK Cell Activity, CD107a Degranulation Amd HLH Related Defective Protein Play Significant Role in the Diagnosis of Primary HLH

Jia Zhang, Zhao Wang, MD

Blood (2016) 128 (22): 4876.

https://doi.org/10.1182/blood.V128.22.4876.4876

Published: 2016

Journal Articles

Novel Flow Cytometry-Based Method Of Affinity Proteomics Revealing Expression, Post-Translational Modification and Proteolysis In Primary Childhood Acute Leukemias

Veronika Kanderova, PhD, Daniela Kuzilkova, MSc, Jan Stuchly, MSc, Weiwei Wu, MD, Anders Holm, PhD, Heidi Slåstad, MD, Karel Fiser, Ondrej Hrusak, Fridtjof Lund-Johansen, MD, PhD, Tomas Kalina, MD, PhD

Blood (2013) 122 (21): 2553.

https://doi.org/10.1182/blood.V122.21.2553.2553

Published: 2013

Journal Articles

Use of the Anti-CD20 Antibody Rituximab In the Treatment of Epstein-Barr Virus-Induced Hemophagocytic Lymphohistiocytosis

Deepakbabu Chellapandian, MD, Susan Wiener, Kristin Zelley, Kim E. Nichols, MD

Blood (2011) 118 (21): 2178.

https://doi.org/10.1182/blood.V118.21.2178.2178

Published: 2011

Journal Articles

Identification of a De Novo UNC13D L1000P Mutation in a Familial Hemophagocytic Lymphohistiocytosis Patient

Hongxing Liu, MD, Fang Wang, MD, Juan Zhu, MD, Hui Wang, MD, Ping Wu, MD, Wen Teng, Xu Han, Jianfeng Zhang, Ping Zhu, MD, Tong Wu, MD, Chunrong Tong, MD

Blood (2011) 118 (21): 4927.

https://doi.org/10.1182/blood.V118.21.4927.4927

Published: 2011

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

High Frequency of Familial Hemophagocytic Lymphocytosis Associated Immune Gene Defects In Refractory Viral Infection of Unknown Origin

Chunrong Tong, MD, Hongxing Liu, Jianjun Xie, MD, Hui Wang, MD, Xian Zhang, MD, Fang Wang, Juan Zhu, Wen Teng, Jiangying Gu, MD, Yali Zhang, MD, Wenjun Ling, MD, Tong Wu, MD, Dao-Pei Lu, MD

Blood (2010) 116 (21): 2775.

https://doi.org/10.1182/blood.V116.21.2775.2775

Published: 2010

Journal Articles

Germline Mutations within the IL2-Inducible T Cell Kinase Impede T Cell Differentiation or Survival, Cause Protein Destabilisation, Loss of Membrane Recruitment and Lead to Severe EBV Lymphoproliferation

Rene Martin Linka, Kirsten Huck, Frank Krux, Polina Stepenski, Cindy Synaeve, Kim Vettenranta, MD, PhD, Rene Deenen, Ingrid Müller-Fleckenstein, Yvonne Linka, Sebastian Ginzel, Anne Halenius, Karl Köhrer, Bernhard Fleckenstein, Hans Jürgen Laws, Roland Hartig, Burkhart Schraven, Sylvain Latour, Arndt Borkhardt, MD

Blood (2010) 116 (21): 280.

https://doi.org/10.1182/blood.V116.21.280.280

Published: 2010

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

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

IgA and IgG Hypogammaglobulinemia Does Not Predict for Recurrent Infection Risk and Persists Despite Therapeutic Response in Patients with Waldentrom's Macroglobulinemia.

Zachary Hunter, Robert Manning, Christina Hanzis, Bryan Ciccarelli, Thea Ioakimidis, MS, Christopher J Patterson, Megan Lewicki, Hsuiyi Tseng, Ping Gong, Xia Liu, MD, Yangsheng Zhou, MD, PhD, Guang Yang, PhD, Jenny Sun, MD, Lian Xu, Patricia Sheehy, NP, Massimo Morra, MD, Steven Treon, MD, PhD

Blood (2009) 114 (22): 1947.

https://doi.org/10.1182/blood.V114.22.1947.1947

Published: 2009

Journal Articles

IgA and IgG Hypogammaglobulinemia Is a Constitutive Feature in Most Waldenstrom’s Macroglobulinemia Patients and May Be Related to Mutations Associated with Common Variable Immunodeficiency Disorder (CVID)

Steven Treon, MD, PhD, Zachary Hunter, Bryan Ciccarelli, Yangsheng Zhou, MD, Christina Hanzis, Robert Manning, Leukothea Ioakimidis, PhD, Lian Xu, Christopher Patterson, MD, Massimo Morra, MD

Blood (2008) 112 (11): 3749.

https://doi.org/10.1182/blood.V112.11.3749.3749

Published: 2008

NARROW

Pediatric hemophagocytic lymphohistiocytosis

Genetic of Sporadic Hemophagocytic Lymphohistiocytosis

Novel Immune Checkpoint Deficiency and Susceptibility to EBV-Associated Lymphoma

Manufacture of Clinical-Grade Universal Antigen Presenting Cells (UAPC) for the Ex Vivo Expansion and Activation of Natural Killer (NK) Cells

Retrospective Next Generation DNA Sequencing Analysis in Patients with Hemophagocytic Lymphohistiocytosis (HLH) Highlights Genetic Variants Associated with Secondary/Late-Onset Disease

Genetic Defects Affecting Lymphocyte Cytotoxicity in Epstein-Barr Virus-Associated T/NK-Cell Lymphoproliferative Diseases

L-DEP Is an Effective Treatment for Adult and Adolescent Patients with Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis

Pedigree Gene Investigation and Parameters of NK Cell Activity, CD107a Degranulation Amd HLH Related Defective Protein Play Significant Role in the Diagnosis of Primary HLH

Novel Flow Cytometry-Based Method Of Affinity Proteomics Revealing Expression, Post-Translational Modification and Proteolysis In Primary Childhood Acute Leukemias

Use of the Anti-CD20 Antibody Rituximab In the Treatment of Epstein-Barr Virus-Induced Hemophagocytic Lymphohistiocytosis

Identification of a De Novo UNC13D L1000P Mutation in a Familial Hemophagocytic Lymphohistiocytosis Patient

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

High Frequency of Familial Hemophagocytic Lymphocytosis Associated Immune Gene Defects In Refractory Viral Infection of Unknown Origin

Germline Mutations within the IL2-Inducible T Cell Kinase Impede T Cell Differentiation or Survival, Cause Protein Destabilisation, Loss of Membrane Recruitment and Lead to Severe EBV Lymphoproliferation

X-linked lymphoproliferative syndromes: brothers or distant cousins?

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

IgA and IgG Hypogammaglobulinemia Does Not Predict for Recurrent Infection Risk and Persists Despite Therapeutic Response in Patients with Waldentrom's Macroglobulinemia.

IgA and IgG Hypogammaglobulinemia Is a Constitutive Feature in Most Waldenstrom’s Macroglobulinemia Patients and May Be Related to Mutations Associated with Common Variable Immunodeficiency Disorder (CVID)

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American Society of Hematology

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American Society of Hematology

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