J. Chapin

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Adherence to guidelines for perioperative management of anticoagulation results in decreased bleeding complications: a single-centre experience

M. Desancho, Svetoslava Bardarova, J. Chapin, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Apoptotic death following Fas activation in human oligodendrocyte hybrid cultures

S. Cook, X. Ming, P. Dowling, 2002, Journal of neuroscience research.

Bleeding Diatheses: Approach to the Patient Who Bleeds or Has Abnormal Coagulation.

J. Chapin, Marcia N. Paddock, 2016, Primary care.

Fibrinolysis and the control of blood coagulation.

K. Hajjar, J. Chapin, 2015, Blood reviews.

Peri- and Postpartum Management of Patients With Factor XI Deficiency

J. Bussel, G. F. Gerber, M. Desancho, 2019, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Clinical presentations, risk factors, treatment and outcomes in patients with splanchnic vein thrombosis: a single-center experience

M. Desancho, E. DeFilippis, J. Chapin, 2016, Journal of Thrombosis and Thrombolysis.

Pulmonary embolism in a patient with congenital afibrinogenemia

M. Desancho, J. Chapin, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

C5b-9 and MASP2 deposition in skin and bone marrow microvasculature characterize hematopoietic stem cell transplant-associated thrombotic microangiopathy

J. Atkinson, A. Chadburn, J. Laurence, 2022, Bone Marrow Transplantation.

The safety of chronic antithrombotic therapy in patients with factor XI deficiency

P. Christos, M. Desancho, J. Chapin, 2017, British journal of haematology.

Platelets and platelet-derived factor Va confer hemostatic competence in complete factor V deficiency.

N. Key, P. Durda, J. Chapin, 2015, Blood.

Hematopoietic transplant-associated thrombotic microangiopathy: case report and review of diagnosis and treatments.

K. van Besien, J. Laurence, Peter A Forsberg, 2014, Clinical advances in hematology & oncology : H&O.

Risk Factors and Treatment Strategies in Patients With Retinal Vascular Occlusions

P. Christos, M. Desancho, J. Chapin, 2015, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Eculizumab in the treatment of refractory idiopathic thrombotic thrombocytopenic purpura

B. Weksler, J. Laurence, C. Magro, 2012, British journal of haematology.

Gender and duration of disease differentiate responses to rituximab–dexamethasone therapy in adults with immune thrombocytopenia

J. Zehnder, Haiyu Zhang, J. Bussel, 2016, American journal of hematology.

Platelet-derived growth factor-alpha receptor-positive oligodendroglia are frequent in multiple sclerosis lesions.

J. Menonna, P. Dowling, Y. Maeda, 2001, Annals of neurology.

Gene Therapy for Hemophilia: Progress to Date

P. Monahan, John C Chapin, Paul Edward Monahan, 2017, BioDrugs.

Outcomes in Patients With Hemophilia and von Willebrand Disease Undergoing Invasive or Surgical Procedures

P. Christos, Paul Christos, M. Desancho, 2017, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Von Willebrand disease in the elderly: clinical perspectives

J. Chapin, 2018, Clinical interventions in aging.

BAX 335 hemophilia B gene therapy clinical trial results - potential impact of CpG sequences on gene expression.

R. Samulski, B. Konkle, I. Bilic, 2020, Blood.

An update on the US adult thalassaemia population: a report from the CDC thalassaemia treatment centres

E. Neufeld, J. Boudreaux, E. Vichinsky, 2021, British journal of haematology.

The role of complement activation in thrombosis and hemolytic anemias.

D. Kleinert, J. Laurence, J. Chapin, 2016, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

MASP2 levels are elevated in thrombotic microangiopathies: association with microvascular endothelial cell injury and suppression by anti‐MASP2 antibody narsoplimab

J. Laurence, J. Chapin, J. Ahamed, 2020, Clinical and experimental immunology.

Thrombelastograph Analysis After Heparin Neutralization with Protamine and Heparinase During Cardiopulmonary Bypass

A. Stammers, J. Chapin, C. Forst, 1994, The Journal of ExtraCorporeal Technology.

Combined factor V and factor VIII deficiency: a report of a case, genetic analysis, and response to desmopressin acetate.

J. Laurence, J. Chapin, C. Gibb, 2012, Clinical advances in hematology & oncology : H&O.

Platelet‐derived growth factor‐α receptor‐positive oligodendroglia are frequent in multiple sclerosis lesions

J. Menonna, P. Dowling, Y. Maeda, 2001, Annals of neurology.

Complement factor H mutations are present in ADAMTS13-deficient, ticlopidine-associated thrombotic microangiopathies.

Richard J. H. Smith, J. Laurence, J. Chapin, 2013, Blood.

Use of eculizumab in the treatment of a case of refractory, ADAMTS13‐deficient thrombotic thrombocytopenic purpura: additional data and clinical follow‐up

J. Laurence, J. Chapin, H. Tsai, 2013, British journal of haematology.

Standard Dose Rituximab and 3 4-Day Cycles of Dexamethasone (R+3D) Appears Curative in Females with ITP < 12 Months Duration

J. Bussel, J. Chapin, J. Oved, 2015 .

Gene Therapy for Hemophilia: Progress to Date

P. Monahan, J. Chapin, 2017, BioDrugs.