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Journal Articles

Bleeding Phenotype Does Not Appear to Correlate with Factor VIII Levels or Genetic Mutation in an Exclusive Pediatric Cohort of Hemophilia a Carriers

Joanna Larson, Katherine Addy, Deborah L. Brown, Nidra Rodriguez, Neethu M Menon, Miguel Escobar, Lakshmi Srivaths

Blood (2022) 140 (Supplement 1): 8458–8459.

https://doi.org/10.1182/blood-2022-160230

Published: 2022

Journal Articles

Appearance of High-Affinity Antibodies Precedes Clinical Diagnosis of FVIII Inhibitors - Preliminary Analysis from the Hemophilia Inhibitor PUP Study (HIPS)

Birgit M Reipert, PhD, Bagirath Gangadharan, PhD, Christoph J Hofbauer, PhD, Fritz Scheiflinger, PhD, Joel Bowen, Elizabeth Donnachie, PhD, Karen Fijvandraat, MD, Ralph A. Gruppo, MD, Jenny Klintman, MD PhD, Christoph Male, MD, Catherine E. McGuinn, MD, Shannon L. Meeks, MD, Michael Recht, MD PhD, M V Ragni, MD, Hassan M Yaish, Elena Santagostino, MD PhD, Deborah L Brown, MD

Blood (2016) 128 (22): 328.

https://doi.org/10.1182/blood.V128.22.328.328

Published: 2016

Journal Articles

No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation

Veronica H. Flood, Kenneth D. Friedman, Joan Cox Gill, Sandra L. Haberichter, Pamela A. Christopherson, Brian R. Branchford, Raymond G. Hoffmann, Thomas C. Abshire, Amy L. Dunn, Jorge A. Di Paola, W. Keith Hoots, Deborah L. Brown, Cindy Leissinger, Jeanne M. Lusher, Margaret V. Ragni, Amy D. Shapiro, Robert R. Montgomery

Blood (2013) 121 (18): 3742–3744.

https://doi.org/10.1182/blood-2012-12-471672

Published: 2013

Journal Articles

Correlates of spontaneous clearance of hepatitis C virus among people with hemophilia

Mingdong Zhang, Philip S. Rosenberg, Deborah L. Brown, Liliana Preiss, Barbara A. Konkle, M. Elaine Eyster, James J. Goedert, for the Second Multicenter Hemophilia Cohort Study

Blood (2006) 107 (3): 892–897.

https://doi.org/10.1182/blood-2005-07-2781

Published: 2006

Journal Articles

Response of Diamond-Blackfan anemia to metoclopramide: evidence for a role for prolactin in erythropoiesis

Janis L. Abkowitz, Gerard Schaison, Farid Boulad, Deborah L. Brown, George R. Buchanan, Christine A. Johnson, Jeffrey C. Murray, Kathleen M. Sabo

Blood (2002) 100 (8): 2687–2690.

https://doi.org/10.1182/blood.V100.8.2687

Published: 2002

Journal Articles

A naturally occurring mutation near the amino terminus of αIIb defines a new region involved in ligand binding to αIIbβ3

Ramesh B. Basani, Deborah L. French, Gaston Vilaire, Deborah L. Brown, Fangping Chen, Barry S. Coller, Jerry M. Derrick, T. Kent Gartner, Joel S. Bennett, Mortimer Poncz

Blood (2000) 95 (1): 180–188.

https://doi.org/10.1182/blood.V95.1.180

Published: 2000

Journal Articles

A Leu 117 → Trp Mutation Within the RGD-Peptide Cross-Linking Region of β3 Results in Glanzmann Thrombasthenia by Preventing αIIbβ3 Export to the Platelet Surface

Ramesh B. Basani, Deborah L. Brown, Gaston Vilaire, Joel S. Bennett, Mortimer Poncz

Blood (1997) 90 (8): 3082–3088.

https://doi.org/10.1182/blood.V90.8.3082

Published: 1997

NARROW

Bleeding Phenotype Does Not Appear to Correlate with Factor VIII Levels or Genetic Mutation in an Exclusive Pediatric Cohort of Hemophilia a Carriers

Appearance of High-Affinity Antibodies Precedes Clinical Diagnosis of FVIII Inhibitors - Preliminary Analysis from the Hemophilia Inhibitor PUP Study (HIPS)

No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation

Correlates of spontaneous clearance of hepatitis C virus among people with hemophilia

Response of Diamond-Blackfan anemia to metoclopramide: evidence for a role for prolactin in erythropoiesis

A naturally occurring mutation near the amino terminus of αIIb defines a new region involved in ligand binding to αIIbβ3

A Leu 117 → Trp Mutation Within the RGD-Peptide Cross-Linking Region of β3 Results in Glanzmann Thrombasthenia by Preventing αIIbβ3 Export to the Platelet Surface

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ASH Publications

American Society of Hematology

Bleeding Phenotype Does Not Appear to Correlate with Factor VIII Levels or Genetic Mutation in an Exclusive Pediatric Cohort of Hemophilia a Carriers

Appearance of High-Affinity Antibodies Precedes Clinical Diagnosis of FVIII Inhibitors - Preliminary Analysis from the Hemophilia Inhibitor PUP Study (HIPS)

No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation

Correlates of spontaneous clearance of hepatitis C virus among people with hemophilia

Response of Diamond-Blackfan anemia to metoclopramide: evidence for a role for prolactin in erythropoiesis

A naturally occurring mutation near the amino terminus of αIIb defines a new region involved in ligand binding to αIIbβ3

A Leu 117 → Trp Mutation Within the RGD-Peptide Cross-Linking Region of β3 Results in Glanzmann Thrombasthenia by Preventing αIIbβ3 Export to the Platelet Surface

Email alerts

ASH Publications

American Society of Hematology

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