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Journal Articles

The Signature Program, a Distinctive Tissue Agnostic Trial Model for Molecularly Pre-Selected Hematological and Solid Tumor Patients

Frank Giles, MD MB, FRCPI, FRCPath, Sarina A. Piha-Paul, MD, Alexander I. Spira, PhD MD FACP, Fadi Braiteh, MD CPI, Julio Antonio Peguero, MD, Daniel L. Spitz, MD FACP, James A. Knost, MD, Lee Schwartzberg, MD FACP, Steven Stein, MD, August J. Salvado, MD, Claudia Lebedinsky, MD, Barinder Kang, PhD, Eric Slosberg, PhD

Blood (2014) 124 (21): 4818.

https://doi.org/10.1182/blood.V124.21.4818.4818

Published: 2014

Journal Articles

Incidence of SCN-Assoicated Gene Mutations in Severe Congenital Neutropenia Patients in North America

Jun Xia, Ph.D, Audrey Anna Bolyard, R.N., B.S., Elin Rodger, Steven Stein, MD, Andrew AG Aprikyan, PhD, David C. Dale, MD, Daniel C. Link, MD

Blood (2008) 112 (11): 3553.

https://doi.org/10.1182/blood.V112.11.3553.3553

Published: 2008

Journal Articles

Genotype-Phenotype Associations in Patients with Severe Congenital Neutropenia.

Philip S. Rosenberg, PhD, Steven Stein, M.D., Elin Rodger, Audrey Anna Bolyard, R.N.,B.S., Mary Ann Bonilla, M.D., Yigal Dror, M.D., George Kannourakis, M.D., Peter E. Newburger, M.D., Laurence A. Boxer, M.D., Blanche P. Alter, M.D.,M.P.H., David C. Dale, M.D.

Blood (2006) 108 (11): 502.

https://doi.org/10.1182/blood.V108.11.502.502

Published: 2006

Journal Articles

Unique Evidence for Autosomal Dominant Inheritance of Severe Congenital Neutropenia.

Laurence A. Boxer, MD, Steven Stein, MD, Danielle Buckley, Sandhya Subramanian, Audrey Anna Bolyard, BS, RN, Maynard V. Olson, MD, David C. Dale, MD

Blood (2004) 104 (11): 1457.

https://doi.org/10.1182/blood.V104.11.1457.1457

Published: 2004

Journal Articles

Mutations in the Gene for Neutrophil Elastase in Severe Congenital Neutropenia Are Heterozygous and of Male Origin.

Steven Stein, MD, Marcia Paddock, Audrey Anna Bolyard, BS, RN, Chris Raymond, PhD, Maynard Olson, PhD, Andrew Aprikyan, PhD, David C. Dale, MD

Blood (2004) 104 (11): 1455.

https://doi.org/10.1182/blood.V104.11.1455.1455

Published: 2004

Journal Articles

An IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in men infected with human immunodeficiency virus

Charles B. Foster, Thomas Lehrnbecher, Susan Samuels, Steven Stein, Femke Mol, Julie A. Metcalf, Kathleen Wyvill, Seth M. Steinberg, Joseph Kovacs, Andrew Blauvelt, Robert Yarchoan, Stephen J. Chanock

Blood (2000) 96 (7): 2562–2567.

https://doi.org/10.1182/blood.V96.7.2562

Published: 2000

NARROW

The Signature Program, a Distinctive Tissue Agnostic Trial Model for Molecularly Pre-Selected Hematological and Solid Tumor Patients

Incidence of SCN-Assoicated Gene Mutations in Severe Congenital Neutropenia Patients in North America

Genotype-Phenotype Associations in Patients with Severe Congenital Neutropenia.

Unique Evidence for Autosomal Dominant Inheritance of Severe Congenital Neutropenia.

Mutations in the Gene for Neutrophil Elastase in Severe Congenital Neutropenia Are Heterozygous and of Male Origin.

An IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in men infected with human immunodeficiency virus

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ASH Publications

American Society of Hematology

The Signature Program, a Distinctive Tissue Agnostic Trial Model for Molecularly Pre-Selected Hematological and Solid Tumor Patients

Incidence of SCN-Assoicated Gene Mutations in Severe Congenital Neutropenia Patients in North America

Genotype-Phenotype Associations in Patients with Severe Congenital Neutropenia.

Unique Evidence for Autosomal Dominant Inheritance of Severe Congenital Neutropenia.

Mutations in the Gene for Neutrophil Elastase in Severe Congenital Neutropenia Are Heterozygous and of Male Origin.

An IL6 promoter polymorphism is associated with a lifetime risk of development of Kaposi sarcoma in men infected with human immunodeficiency virus

Email alerts

ASH Publications

American Society of Hematology

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