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

1-16 of 16

Sort by

Sort Order Select

Journal Articles

Natural history study of patients with familial platelet disorder with associated myeloid malignancy

Blood (2023) 142 (25): 2146–2158.

https://doi.org/10.1182/blood.2023019746

Published: 2023

Includes: Supplemental data

Journal Articles

Bone Marrow, Laboratory, and Clinical Features in Pediatric Patients with RUNX1 Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)

Seila De Leon, Michelly Sampaio De Melo, Nisha Patel, Alina Dulau Florea, Irina Maric, Raul C. Braylan, Weixin Wang, Matthew Merguerian, Elizabeth J. Andrews, Lea Cunningham, David J. Young, Shawn Chong, Natalie Deuitch, Joie Davis, Kathleen Craft, Theo Heller, Pamela Frischmeyer-Guerrerio, Paul Pu Liu, Katherine R. Calvo

Blood (2023) 142 (Supplement 1): 4109.

https://doi.org/10.1182/blood-2023-187600

Published: 2023

Journal Articles

Genomic Landscape of RUNX1 -Familial Platelet Disorder with Myeloid Malignancies Reveals Rising Clonal Hematopoiesis

Kai Yu, Matthew Merguerian, Natalie Deuitch, Erica Bresciani, Joie Davis, Kathleen Craft, Lea C. Cunningham, Paul P. Liu

Blood (2021) 138 (Supplement 1): 1090.

https://doi.org/10.1182/blood-2021-151781

Published: 2021

Journal Articles

Dominant activating RAC2 mutation with lymphopenia, immunodeficiency, and cytoskeletal defects

Blood (2019) 133 (18): 1977–1988.

https://doi.org/10.1182/blood-2018-11-886028

Published: 2019

Includes: Multimedia, Supplemental data

Journal Articles

Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations

Susan Price, Pamela A. Shaw, Amy Seitz, Gyan Joshi, Joie Davis, Julie E. Niemela, Katie Perkins, Ronald L. Hornung, Les Folio, Philip S. Rosenberg, Jennifer M. Puck, Amy P. Hsu, Bernice Lo, Stefania Pittaluga, Elaine S. Jaffe, Thomas A. Fleisher, V. Koneti Rao, Michael J. Lenardo

Blood (2014) 123 (13): 1989–1999.

https://doi.org/10.1182/blood-2013-10-535393

Published: 2014

Includes: Supplemental data

Journal Articles

Clinical Spectrum of RAS-Associated Autoimmune Leukoproliferative Disorder (RALD): A Distinct Clinical Entity Mimicking Juvenile Myelomonocytioc Leukemia (JMML) or Chronic Myelomonocytic Leukemia (CMML)

V. Koneti Rao, Joao Bosco Oliveira, MD, PhD, Julie Niemela, PhD, Joie Davis, NP, Susan Price, Hyesun Kuehn, Katherine R Calvo, MD, PhD, Stefania Pittaluga, Eric J. Werner, MD, Joohee Lee, MD, Mustafa Barbour, MD, Marc Natter, MD, Mignon L. Loh, MD, Thomas A Fleisher

Blood (2012) 120 (21): 1033.

https://doi.org/10.1182/blood.V120.21.1033.1033

Published: 2012

Journal Articles

Expanding Spectrum of Malignancies in ALPS: A Cancer Predisposing Syndrome?.

Katie Perkins, NP, Joie Davis, NP, Susan Price, RN, Julie Niemela, PhD, Andreas R. Huber, MD, Donna A. Wall, MD, Stefania Pittaluga, MD, PhD, Thomas A. Fleisher, MD, V. Koneti Rao, MD

Blood (2012) 120 (21): 2149.

https://doi.org/10.1182/blood.V120.21.2149.2149

Published: 2012

Journal Articles

Mycophenolate Mofetil and Thrombopoietin Receptor Agonists in the Treatment of Refractory Thrombocytopenia in Patients with Autoimmune Lymphoproliferative Syndrome

Leejah Chang, MD, Susan Price, RN, Katie Perkins, NP, Joie Davis, NP, Patricia Aldridge, CRN, Michael Recht, MD, PhD, John Kelleher, MD, V. Koneti Rao, MD

Blood (2011) 118 (21): 2218.

https://doi.org/10.1182/blood.V118.21.2218.2218

Published: 2011

Journal Articles

Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

Julie E. Niemela, Lianghao Lu, Thomas A. Fleisher, Joie Davis, Iusta Caminha, Marc Natter, Laurel A. Beer, Kennichi C. Dowdell, Stefania Pittaluga, Mark Raffeld, V. Koneti Rao, João B. Oliveira

Blood (2011) 117 (10): 2883–2886.

https://doi.org/10.1182/blood-2010-07-295501

Published: 2011

Includes: Supplemental data

Journal Articles

Causes and Consequences of Splenectomy In ALPS-FAS

Susan Price, Pamela Shaw, Jennifer Kirk, Joie Davis, Katie Perkins, Fred Gill, Thomas Fleisher, V. Koneti Rao

Blood (2010) 116 (21): 3908.

https://doi.org/10.1182/blood.V116.21.3908.3908

Published: 2010

Journal Articles

Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome

Kennichi C. Dowdell, Julie E. Niemela, Susan Price, Joie Davis, Ronald L. Hornung, João Bosco Oliveira, Jennifer M. Puck, Elaine S. Jaffe, Stefania Pittaluga, Jeffrey I. Cohen, Thomas A. Fleisher, V. Koneti Rao

Blood (2010) 115 (25): 5164–5169.

https://doi.org/10.1182/blood-2010-01-263145

Published: 2010

Includes: Supplemental data

Journal Articles

Somatic Fas Mutations Account for Nearly One Third of Autoimmune Lymphoproliferative Syndrome (ALPS) Cases with Previously Unknown Genetic Mutations.

Kennichi Dowdell, PhD, Julie Niemela, Susan Price, Joie Davis, Katie Perkins, Janet Dale, Jennifer M. Puck, MD, Joao Bosco Oliveira, MD, PhD, Jeffrey Cohen, MD, Thomas Fleisher, MD, V. Koneti Rao, MD

Blood (2009) 114 (22): 710.

https://doi.org/10.1182/blood.V114.22.710.710

Published: 2009

Journal Articles

Identifying Biomarkers in the Autoimmune Lymphoproliferative Syndrome (ALPS): IL-18, TNF-á, Serum Vitamin B12, Soluble FasL, and Plasma IL-10 Levels Are Useful Adjuvant Diagnostic Tools.

Iusta Caminha, Thomas Fleisher, Julie Niemela, Ron Hornung, PhD, Joie Davis, Katie Perkins, Kennichi Dowdell, PhD, Susan Price, RN, Margaret Brown, BSc, V. Koneti Rao, MD, FRCPA, Joao Bosco Oliveira, MD, PhD

Blood (2009) 114 (22): 1647.

https://doi.org/10.1182/blood.V114.22.1647.1647

Published: 2009

Journal Articles

Use of Rituximab for Refractory Immune Cytopenias Associated with Autoimmune Lymphoproliferative Syndrome (ALPS).

Janet K. Dale, RN, Susan Price, RN, Jean Tretler, RN, Patricia Aldridge, RN, Stephanie Montague, RN MSN, Joie Davis, APRN, Fred Gill, MD, Kip R. Hartman, MD, Linda C. Stork, MD, David J. Gnarra, MD, Lakshmanan Krishnamurti, MD, Jennifer Puck, MD, Thomas Fleisher, MD, V. Koneti Rao, MD

Blood (2007) 110 (11): 1319.

https://doi.org/10.1182/blood.V110.11.1319.1319

Published: 2007

Journal Articles

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency

Javier Chinen, Joie Davis, Suk See De Ravin, Beverly N. Hay, Amy P. Hsu, Gilda F. Linton, Nora Naumann, Effie Y. H. Nomicos, Christopher Silvin, Jean Ulrick, Narda L. Whiting-Theobald, Harry L. Malech, Jennifer M. Puck

Blood (2007) 110 (1): 67–73.

https://doi.org/10.1182/blood-2006-11-058933

Published: 2007

Journal Articles

Ex Vivo Gene Therapy of a Preadolescent with X-Linked Severe Combined Immunodeficiency.

Javier Chinen, MD, PhD, Jennifer M. Puck, MD, Joie Davis, RN, Gilda F. Linton, Med T, Narda L. Whiting-Theobald, BA, Patricia C. Woltz, RN, Rebecca H. Buckley, MD, Harry L. Malech, MD

Blood (2004) 104 (11): 410.

https://doi.org/10.1182/blood.V104.11.410.410

Published: 2004

NARROW

Natural history study of patients with familial platelet disorder with associated myeloid malignancy

Bone Marrow, Laboratory, and Clinical Features in Pediatric Patients with RUNX1 Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)

Genomic Landscape of RUNX1 -Familial Platelet Disorder with Myeloid Malignancies Reveals Rising Clonal Hematopoiesis

Dominant activating RAC2 mutation with lymphopenia, immunodeficiency, and cytoskeletal defects

Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations

Clinical Spectrum of RAS-Associated Autoimmune Leukoproliferative Disorder (RALD): A Distinct Clinical Entity Mimicking Juvenile Myelomonocytioc Leukemia (JMML) or Chronic Myelomonocytic Leukemia (CMML)

Expanding Spectrum of Malignancies in ALPS: A Cancer Predisposing Syndrome?.

Mycophenolate Mofetil and Thrombopoietin Receptor Agonists in the Treatment of Refractory Thrombocytopenia in Patients with Autoimmune Lymphoproliferative Syndrome

Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

Causes and Consequences of Splenectomy In ALPS-FAS

Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome

Somatic Fas Mutations Account for Nearly One Third of Autoimmune Lymphoproliferative Syndrome (ALPS) Cases with Previously Unknown Genetic Mutations.

Identifying Biomarkers in the Autoimmune Lymphoproliferative Syndrome (ALPS): IL-18, TNF-á, Serum Vitamin B12, Soluble FasL, and Plasma IL-10 Levels Are Useful Adjuvant Diagnostic Tools.

Use of Rituximab for Refractory Immune Cytopenias Associated with Autoimmune Lymphoproliferative Syndrome (ALPS).

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency

Ex Vivo Gene Therapy of a Preadolescent with X-Linked Severe Combined Immunodeficiency.

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only