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Journal Articles

Dehydrated Hereditary Stomatocytosis in a Multi-Generational American Family with a KCNN4 Gardos Channel Mutation

Sasha Waldstein, MD, Sarah E. Arnold-Croop, MS, Laura Carrel, PhD, M. Elaine Eyster, MD

Blood (2020) 136 (Supplement 1): 11.

https://doi.org/10.1182/blood-2020-137481

Published: 2020

Journal Articles

Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants

Peter H. Cygan, MD, Sarah E. Arnold-Croop, MS, Elizabeth A. Weidman, BS, Fang Chen, PhD, Dajiang J. Liu, PhD, M. Elaine Eyster, MD, Laura Carrel, PhD

Blood (2019) 134 (Supplement_1): 1125.

https://doi.org/10.1182/blood-2019-126026

Published: 2019

Journal Articles

Elevated Von Willebrand Factor May Abrogate Bleeding Phenotype in a Male with a Non-Null F8 Mutation

Peter H. Cygan, MD, Sarah E. Arnold-Croop, MS, Elizabeth A. Weidman, BS, Laura Carrel, PhD, M. Elaine Eyster, MD

Blood (2018) 132 (Supplement 1): 3787.

https://doi.org/10.1182/blood-2018-99-116905

Published: 2018

Journal Articles

Random X-Chromosome Inactivation in Hemophilia A Carriers Does Not Fully Attenuate Bleeding Risk

Peter H. Cygan, MD, Elizabeth A. Weidman, BS, Lan Kong, PhD, Laura Carrel, PhD, M. Elaine Eyster, MD

Blood (2017) 130 (Supplement 1): 3676.

https://doi.org/10.1182/blood.V130.Suppl_1.3676.3676

Published: 2017

Journal Articles

Role of Von Willebrand Factor in Female Carriers from an Extended Family with Mild Hemophilia A

Tomilya Simmons, Peter H. Cygan, MD, Laura Carrel, PhD, M. Elaine Eyster, MD

Blood (2015) 126 (23): 3537.

https://doi.org/10.1182/blood.V126.23.3537.3537

Published: 2015

Journal Articles

Correlation of X Chromosome Inactivation Skewing and Bleeding Phenotype in Obligate Carriers of Hemophilia A

Peter H. Cygan, MD, Laura Carrel, PhD, M. Elaine Eyster, MD

Blood (2015) 126 (23): 2285.

https://doi.org/10.1182/blood.V126.23.2285.2285

Published: 2015

NARROW

Dehydrated Hereditary Stomatocytosis in a Multi-Generational American Family with a KCNN4 Gardos Channel Mutation

Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants

Elevated Von Willebrand Factor May Abrogate Bleeding Phenotype in a Male with a Non-Null F8 Mutation

Random X-Chromosome Inactivation in Hemophilia A Carriers Does Not Fully Attenuate Bleeding Risk

Role of Von Willebrand Factor in Female Carriers from an Extended Family with Mild Hemophilia A

Correlation of X Chromosome Inactivation Skewing and Bleeding Phenotype in Obligate Carriers of Hemophilia A

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ASH Publications

American Society of Hematology

Dehydrated Hereditary Stomatocytosis in a Multi-Generational American Family with a KCNN4 Gardos Channel Mutation

Bleeding in Mild Hemophilia A Due to a Splice-Site F8 Mutation May be Fully Abrogated By Prothrombotic Gene Variants

Elevated Von Willebrand Factor May Abrogate Bleeding Phenotype in a Male with a Non-Null F8 Mutation

Random X-Chromosome Inactivation in Hemophilia A Carriers Does Not Fully Attenuate Bleeding Risk

Role of Von Willebrand Factor in Female Carriers from an Extended Family with Mild Hemophilia A

Correlation of X Chromosome Inactivation Skewing and Bleeding Phenotype in Obligate Carriers of Hemophilia A

Email alerts

ASH Publications

American Society of Hematology

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