Transfusion and Apheresis Science

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Short Biography of Guest Editor, Dr. Mary Frances Scully

Mary-Frances Scully

DOI: https://doi.org/10.1016/j.transci.2018.07.001

Vol. 57, Issue 4, p445

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Blood coagulation dissected

Edward L.G. Pryzdial, Frank M.H. Lee, Bryan H. Lin, Rolinda L.R. Carter, Tseday Z. Tegegn, Mark J. Belletrutti

DOI: https://doi.org/10.1016/j.transci.2018.07.003

Vol. 57, Issue 4, p449–457

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Introduction to Part 1 of a 3-part theme edition focused on Hereditary Bleeding Disorders

Mary-Frances Scully

DOI: https://doi.org/10.1016/j.transci.2018.07.002

Vol. 57, Issue 4, p446–448

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Bleeding by the numbers: The utility and the limitations of bleeding scores, bleeding prediction tools, and bleeding case definitions

Emily K. Rimmer, Donald S. Houston

DOI: https://doi.org/10.1016/j.transci.2018.07.004

Vol. 57, Issue 4, p458–462

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Current approaches to diagnostic testing in von Willebrand Disease

Emily Southard Rao, Christopher J. Ng

DOI: https://doi.org/10.1016/j.transci.2018.07.005

Vol. 57, Issue 4, p463–465

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State of the art in factor XIII laboratory assessment

Michael A. Durda, Alisa S. Wolberg, Bryce A. Kerlin

DOI: https://doi.org/10.1016/j.transci.2018.07.006

Vol. 57, Issue 6, p700–704

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Issues complicating precision dosing for factor VIII prophylaxis

Leonard A. Valentino, Peter L. Turecek, Herbert Gritsch, Saulius Butenas, Kenneth G. Mann

DOI: https://doi.org/10.1016/j.transci.2018.07.007

Vol. 57, Issue 4, p472–479

Open Access

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Novel assays in the coagulation laboratory: a clinical and laboratory perspective

Jennifer Teichman, Hina Razzaq Chaudhry, Michelle Sholzberg

DOI: https://doi.org/10.1016/j.transci.2018.07.008

Vol. 57, Issue 4, p480–484

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Laboratory diagnosis of inherited platelet function disorders

Margaret L. Rand, Emily C. Reddy, Sara J. Israels

DOI: https://doi.org/10.1016/j.transci.2018.07.009

Vol. 57, Issue 4, p485–493

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Inherited platelet functional disorders: General principles and practical aspects of management

Adrienne Lee, Man-Chiu Poon

DOI: https://doi.org/10.1016/j.transci.2018.07.010

Vol. 57, Issue 4, p494–501

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Treatment and prevention of bleeding in congenital hemophilia A patients with inhibitors

Jerome M. Teitel

DOI: https://doi.org/10.1016/j.transci.2018.07.011

Vol. 57, Issue 4, p466–471

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The current and future role of plasma-derived clotting factor concentrate in the treatment of haemophilia A

Barry Kevane, Niamh O’Connell

DOI: https://doi.org/10.1016/j.transci.2018.07.012

Vol. 57, Issue 4, p502–506

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Introduction to part two of a three-part theme on hereditary bleeding disorders

Mary-Frances Scully

DOI: https://doi.org/10.1016/j.transci.2018.10.008

Vol. 57, Issue 6, p698–699

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Management of rare coagulation disorders in 2018

Shilpa Jain, Suchitra S. Acharya

DOI: https://doi.org/10.1016/j.transci.2018.10.009

Vol. 57, Issue 6, p705–712

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The unusual pattern of hereditary bleeding disorders in the province of Newfoundland and Labrador—Canada’s most Eastern Province

Mary-Frances Scully, Jayson Stoffman, Sarah Boyd

DOI: https://doi.org/10.1016/j.transci.2018.10.010

Vol. 57, Issue 6, p713–716

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Management of acquired hemophilia A: Review of current evidence

Janie Charlebois, Georges-Étienne Rivard, Jean St-Louis

DOI: https://doi.org/10.1016/j.transci.2018.10.011

Vol. 57, Issue 6, p717–720

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Management of acquired von Willebrand syndrome

Janie Charlebois, Georges-Étienne Rivard, Jean St-Louis

DOI: https://doi.org/10.1016/j.transci.2018.10.012

Vol. 57, Issue 6, p721–723

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Acquired factor XIII deficiency: A review

Matthew Tak Sheng Yan, Natalia Rydz, Dawn Goodyear, Michelle Sholzberg

DOI: https://doi.org/10.1016/j.transci.2018.10.013

Vol. 57, Issue 6, p724–730

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Supply and demand for hemophilia treatments—Systems-based approaches to mitigate the risk

J.M. Stoffman, S. Jackson, J. Teitel

DOI: https://doi.org/10.1016/j.transci.2018.10.014

Vol. 57, Issue 6, p731–734

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Iron deficiency and anemia in patients with inherited bleeding disorders

Heather VanderMeulen, Michelle Sholzberg

DOI: https://doi.org/10.1016/j.transci.2018.10.015

Vol. 57, Issue 6, p735–738

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Hereditary Bleeding Disorders

Edited by Mary-Frances Scully

Short Biography of Guest Editor, Dr. Mary Frances Scully

Blood coagulation dissected

Introduction to Part 1 of a 3-part theme edition focused on Hereditary Bleeding Disorders

Bleeding by the numbers: The utility and the limitations of bleeding scores, bleeding prediction tools, and bleeding case definitions

Current approaches to diagnostic testing in von Willebrand Disease

State of the art in factor XIII laboratory assessment

Issues complicating precision dosing for factor VIII prophylaxis

Novel assays in the coagulation laboratory: a clinical and laboratory perspective

Laboratory diagnosis of inherited platelet function disorders

Inherited platelet functional disorders: General principles and practical aspects of management

Treatment and prevention of bleeding in congenital hemophilia A patients with inhibitors

The current and future role of plasma-derived clotting factor concentrate in the treatment of haemophilia A

Introduction to part two of a three-part theme on hereditary bleeding disorders

Management of rare coagulation disorders in 2018

The unusual pattern of hereditary bleeding disorders in the province of Newfoundland and Labrador—Canada’s most Eastern Province

Management of acquired hemophilia A: Review of current evidence

Management of acquired von Willebrand syndrome

Acquired factor XIII deficiency: A review

Supply and demand for hemophilia treatments—Systems-based approaches to mitigate the risk

Iron deficiency and anemia in patients with inherited bleeding disorders