Matthew Goodyer

Sitten, VS, Switzerland

Last Updated: 09/26/2026

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Found 11 publications

Management of systemic lupus erythematosus and antiphospholipid syndrome during CAR-T therapy: insights from two clinical cases.

Management of systemic lupus erythematosus and antiphospholipid syndrome during CAR-T therapy: insights from two clinical cases.

Journal: Immuno-oncology technology
Published: August 20, 2026

Sequential combinations of rapid immunoassays for prompt recognition of heparin-induced thrombocytopenia.

Sequential combinations of rapid immunoassays for prompt recognition of heparin-induced thrombocytopenia.

Journal: Blood
Published: November 01, 2024

Targeted management of coexistent severe thrombophilias-A case report of a successful pregnancy despite paroxysmal nocturnal hemoglobinuria and hereditary protein C deficiency.

Targeted management of coexistent severe thrombophilias-A case report of a successful pregnancy despite paroxysmal nocturnal hemoglobinuria and hereditary protein C deficiency.

Journal: EJHaem
Published: February 14, 2024

Managing argatroban in heparin-induced thrombocytopenia: A retrospective analysis of 729 treatment days in 32 patients with confirmed heparin-induced thrombocytopenia.

Managing argatroban in heparin-induced thrombocytopenia: A retrospective analysis of 729 treatment days in 32 patients with confirmed heparin-induced thrombocytopenia.

Journal: British journal of haematology
Published: January 15, 2022

Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations.

Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations.

Journal: Thrombosis research
Published: June 10, 2020

Rapid and accurate Bayesian diagnosis of heparin-induced thrombocytopenia.

Rapid and accurate Bayesian diagnosis of heparin-induced thrombocytopenia.

Journal: Blood
Published: August 14, 2019

Mutational Epidemiology of Congenital Fibrinogen Disorders.

Mutational Epidemiology of Congenital Fibrinogen Disorders.

Journal: Thrombosis and haemostasis
Published: October 18, 2018

The JAK2 V617F Allele Burden in Latent Myeloproliferative Neoplasms Presenting with Splanchnic Vein Thrombosis.

The JAK2 V617F Allele Burden in Latent Myeloproliferative Neoplasms Presenting with Splanchnic Vein Thrombosis.

Journal: Pathology oncology research : POR
Published: August 31, 2015

Successful treatment with rituximab and mycophenolate mofetil of refractory autoimmune hemolytic anemia post-hematopoietic stem cell transplant for dyskeratosis congenita due to TINF2 mutation.

Successful treatment with rituximab and mycophenolate mofetil of refractory autoimmune hemolytic anemia post-hematopoietic stem cell transplant for dyskeratosis congenita due to TINF2 mutation.

Journal: Pediatric transplantation
Published: August 29, 2013

Allogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphoma.

Allogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphoma.

Journal: British journal of haematology
Published: July 09, 2013

A multi-centre retrospective study of rituximab use in the treatment of relapsed or resistant warm autoimmune haemolytic anaemia.

A multi-centre retrospective study of rituximab use in the treatment of relapsed or resistant warm autoimmune haemolytic anaemia.

Journal: British journal of haematology
Published: April 15, 2013
Showing 1-11 of 11

Last Updated: 09/26/2026