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Use of Social Media in the Practice of Medicine

The American journal of medicine, 2022-02, Vol.135 (2), p.138-140

2022

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Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo

Proceedings of the National Academy of Sciences - PNAS, 2018-08, Vol.115 (33), p.E7748-E7757

2018

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Sex specific definitions of anaemia reflect androgen production - Authors' reply

The Lancet. Haematology, 2022-04, Vol.9 (4), p.e243-e244

2022

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Advancements in haemophilia A and health equity: is it time to redefine severity?

The Lancet. Haematology, 2024-02, Vol.11 (2), p.e90-e92

2024

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Guidelines are needed to advance health equity in hematology

Blood advances, 2024-09

2024

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The Perfect Balance? Managing Heavy Menstrual Bleeding and Dysmenorrhea in a Patient with Hereditary Hemochromatosis and von Willebrand Disease

Journal of pediatric & adolescent gynecology, 2021-02, Vol.34 (1), p.74-76

2021

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Modeling Disorders of Blood Coagulation in the Zebrafish

Current pathobiology reports, 2015-06, Vol.3 (2), p.155-161

2015

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Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome Associated with Enoxaparin Therapy in a Pediatric Patient

Blood, 2021-11, Vol.138 (Supplement 1), p.4269-4269

2021

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Von Willebrand Disease

Hematology/oncology clinics of North America, 2021-12, Vol.35 (6), p.1085-1101

2021

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Findings from the XTEND-Kids Study: Efanesoctocog Alfa for Severe Haemophilia A in Children

Oncology & Haematology, 2023, Vol.19 (2), p.2

2023

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Evaluating Sex-Based Hemoglobin Reference Intervals Using Strict Definitions of Health

Blood, 2023-11, Vol.142 (Supplement 1), p.1084-1084

2023

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Facilitators and Barriers to Accessing Antifibrinolytic and Iron Therapies for Patients Who Menstruate - a Global Healthcare Provider Survey

Blood, 2023-11, Vol.142 (Supplement 1), p.5071-5071

2023

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Quality of Life in Patients with Clinically Severe Von Willebrand Disease: Interim Analysis of Athn 9: A Natural History Study for People with Severe Von Willebrand Disease (VWD)

Blood, 2022-11, Vol.140 (Supplement 1), p.5600-5602

2022

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Is ≥ 100% the magic number to rule out the laboratory diagnosis of von W illebrand disease based on initial testing?

American journal of hematology, 2021-11, Vol.96 (11)

2021

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Assessing the Safety of Various VWF Regimens in Patients with Clinically Severe VWD: A Natural History Study

Blood, 2019-11, Vol.134 (Supplement_1), p.1132-1132

2019

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Evaluating Hemoglobin Thresholds on the Basis of Sex: Preliminary Insights from a Systematic Review

Blood, 2023-11, Vol.142 (Supplement 1), p.7200-7200

2023

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Surprisingly Rapid Onset of Estrogen-Induced Venous Thrombosis in an Animal Model

Blood, 2018-11, Vol.132 (Supplement 1), p.418-418

2018

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Hemophilia A Research Program (HARP): A Novel Study Design for a Multicenter and Decentralized Prospective Observational Longitudinal Cohort Study in Hemophilia A

Blood, 2023-11, Vol.142 (Supplement 1), p.5494-5494

2023

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Real-World Use of Recombinant Von Willebrand Factor in People with Clinically Severe Congenital Von Willebrand Disease: Interim Analysis of Athn 9: A Natural History Study for People with Severe VWD

Blood, 2023-11, Vol.142 (Supplement 1), p.2613-2613

2023

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Depression in adolescent females with heavy menstrual bleeding

The Journal of pediatrics, 2021-09, Vol.240, p.171-176

2021

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Efficacy of Efanesoctocog Alfa on Physical Functioning: Results from the XTEND-1 Phase 3 Clinical Trial in Previously Treated Patients with Hemophilia A

Blood, 2022-11, Vol.140 (Supplement 1), p.5595-5596

2022

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Characteristics and Healthcare Utilization of Patients with Mild or Moderate Hemophilia A in the US - an Analysis from the Picnichealth Cohort

Blood, 2022-11, Vol.140 (Supplement 1), p.2762-2763

2022

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Characteristics and Bleeding Behavior of Females with Mild Hemophilia A: Longitudinal Study from Picnichealth Hemophilia A Database

Blood, 2022-11, Vol.140 (Supplement 1), p.61-62

2022

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Genome Editing of Factor V in Zebrafish Embryos Results in a Severe Hemostatic Defect without Spontaneous Hemorrhage

Blood, 2016-12, Vol.128 (22), p.2565-2565

2016

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Bleeding in Patients with Clinically Severe Von Willebrand Disease: Preliminary Results of Athn 9, a Natural History Study of the Safety, Effectiveness, and Practice of Treatment for People with Severe Von Willebrand Disease (VWD)

Blood, 2020-11, Vol.136 (Supplement 1), p.27-28

2020

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Use of Social Media in the Practice of Medicine

Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo

Sex specific definitions of anaemia reflect androgen production - Authors' reply

Advancements in haemophilia A and health equity: is it time to redefine severity?

Guidelines are needed to advance health equity in hematology

The Perfect Balance? Managing Heavy Menstrual Bleeding and Dysmenorrhea in a Patient with Hereditary Hemochromatosis and von Willebrand Disease

Modeling Disorders of Blood Coagulation in the Zebrafish

Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Syndrome Associated with Enoxaparin Therapy in a Pediatric Patient

Von Willebrand Disease

Findings from the XTEND-Kids Study: Efanesoctocog Alfa for Severe Haemophilia A in Children

Evaluating Sex-Based Hemoglobin Reference Intervals Using Strict Definitions of Health

Facilitators and Barriers to Accessing Antifibrinolytic and Iron Therapies for Patients Who Menstruate - a Global Healthcare Provider Survey

Quality of Life in Patients with Clinically Severe Von Willebrand Disease: Interim Analysis of Athn 9: A Natural History Study for People with Severe Von Willebrand Disease (VWD)

Is ≥ 100% the magic number to rule out the laboratory diagnosis of von W illebrand disease based on initial testing?

Assessing the Safety of Various VWF Regimens in Patients with Clinically Severe VWD: A Natural History Study

Evaluating Hemoglobin Thresholds on the Basis of Sex: Preliminary Insights from a Systematic Review

Surprisingly Rapid Onset of Estrogen-Induced Venous Thrombosis in an Animal Model

Hemophilia A Research Program (HARP): A Novel Study Design for a Multicenter and Decentralized Prospective Observational Longitudinal Cohort Study in Hemophilia A

Real-World Use of Recombinant Von Willebrand Factor in People with Clinically Severe Congenital Von Willebrand Disease: Interim Analysis of Athn 9: A Natural History Study for People with Severe VWD

Depression in adolescent females with heavy menstrual bleeding

Efficacy of Efanesoctocog Alfa on Physical Functioning: Results from the XTEND-1 Phase 3 Clinical Trial in Previously Treated Patients with Hemophilia A

Characteristics and Healthcare Utilization of Patients with Mild or Moderate Hemophilia A in the US - an Analysis from the Picnichealth Cohort

Characteristics and Bleeding Behavior of Females with Mild Hemophilia A: Longitudinal Study from Picnichealth Hemophilia A Database

Genome Editing of Factor V in Zebrafish Embryos Results in a Severe Hemostatic Defect without Spontaneous Hemorrhage

Bleeding in Patients with Clinically Severe Von Willebrand Disease: Preliminary Results of Athn 9, a Natural History Study of the Safety, Effectiveness, and Practice of Treatment for People with Severe Von Willebrand Disease (VWD)

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