Page 1 | Search Results | Blood | American Society of Hematology

1-7 of 7

Sort by

Sort Order Select

Journal Articles

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

Janos Sumegi, Shawnagay V. Nestheide, Michael G. Barnes, Joyce Villanueva, Kejian Zhang, Alexei A. Grom, Alexandra H. Filipovich

Blood (2013) 121 (7): e14–e24.

https://doi.org/10.1182/blood-2012-05-425769

Published: 2013

Includes: Supplemental data

Journal Articles

Gene expression profiling of peripheral blood mononuclear cells from children with active hemophagocytic lymphohistiocytosis

Janos Sumegi, Michael G. Barnes, Shawnagay V. Nestheide, Susan Molleran-Lee, Joyce Villanueva, Kejian Zhang, Kimberly A. Risma, Alexei A. Grom, Alexandra H. Filipovich

Blood (2011) 117 (15): e151–e160.

https://doi.org/10.1182/blood-2010-08-300046

Published: 2011

Includes: Supplemental data

Journal Articles

Functional assessment of perforin C2 domain mutations illustrates the critical role for calcium-dependent lipid binding in perforin cytotoxic function

Ramon Urrea Moreno, Juana Gil, Carmen Rodriguez-Sainz, Elena Cela, Victor LaFay, Brian Oloizia, Andrew B. Herr, Janos Sumegi, Michael B. Jordan, Kimberly A. Risma

Blood (2009) 113 (2): 338–346.

https://doi.org/10.1182/blood-2008-08-172924

Published: 2009

Includes: Supplemental data

Journal Articles

Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family members

Yasuhiro Tabata, Joyce Villanueva, Susan Molleran Lee, Kejian Zhang, Hirokazu Kanegane, Toshio Miyawaki, Janos Sumegi, Alexandra H. Filipovich

Blood (2005) 105 (8): 3066–3071.

https://doi.org/10.1182/blood-2004-09-3651

Published: 2005

Journal Articles

Rapid Detection of SAP Deficiency in Cytotoxic Lymphocytes from Patients with X-Linked Lymphoproliferative Disease and Their Family Members.

Yasuhiro Tabata, MD, Joyce Villanueva, BS, Susan M. Lee, BS, Kejian Zhang, MD, Hirokazu Kanegane, MD, Toshio Miyawaki, MD, Janos Sumegi, MD, Alexandra H. Filipovich, MD

Blood (2004) 104 (11): 3846.

https://doi.org/10.1182/blood.V104.11.3846.3846

Published: 2004

Journal Articles

Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members

Kazuhiro Kogawa, Susan M. Lee, Joyce Villanueva, Daniel Marmer, Janos Sumegi, Alexandra H. Filipovich

Blood (2002) 99 (1): 61–66.

https://doi.org/10.1182/blood.V99.1.61

Published: 2002

Journal Articles

Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease

Janos Sumegi, Dali Huang, Arpad Lanyi, Jack D. Davis, Thomas A. Seemayer, Akihiko Maeda, George Klein, Marco Seri, Hiroshi Wakiguchi, David T. Purtilo, Thomas G. Gross

Blood (2000) 96 (9): 3118–3125.

https://doi.org/10.1182/blood.V96.9.3118

Published: 2000

NARROW

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

Gene expression profiling of peripheral blood mononuclear cells from children with active hemophagocytic lymphohistiocytosis

Functional assessment of perforin C2 domain mutations illustrates the critical role for calcium-dependent lipid binding in perforin cytotoxic function

Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family members

Rapid Detection of SAP Deficiency in Cytotoxic Lymphocytes from Patients with X-Linked Lymphoproliferative Disease and Their Family Members.

Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members

Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease

Email alerts

ASH Publications

American Society of Hematology

Gene-expression signatures differ between different clinical forms of familial hemophagocytic lymphohistiocytosis

Gene expression profiling of peripheral blood mononuclear cells from children with active hemophagocytic lymphohistiocytosis

Functional assessment of perforin C2 domain mutations illustrates the critical role for calcium-dependent lipid binding in perforin cytotoxic function

Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family members

Rapid Detection of SAP Deficiency in Cytotoxic Lymphocytes from Patients with X-Linked Lymphoproliferative Disease and Their Family Members.

Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members

Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only