Search Results - "Gavillet, Mathilde"

Obstetrical Impact of Anti-MUT (Anti-MNS35) Alloimmunization.

Authors: Gavillet, Mathilde Gleich-Nagel, Tobias Legardeur, Helene et al.

Source: Transfusion Medicine & Hemotherapy. Feb2026, p1-7. 7p. 3 Illustrations, 1 Chart.

Indications and contraindications to platelet‐rich plasma injections in musculoskeletal diseases in case of infectious, oncological and haematological comorbidities: A 2025 formal consensus from the GRIIP (International Research Group on Platelet Injections)

Authors: Eymard, Florent Louati, Karine Noel, Éric et al.

Source: Knee Surgery, Sports Traumatology, Arthroscopy. Jun2025, Vol. 33 Issue 6, p2293-2306.

Acquired haemophilia A in the postpartum and risk of relapse in subsequent pregnancies: A systematic literature review.

Authors: Dewarrat, Natacha Gavillet, Mathilde Angelillo‐Scherrer, Anne et al.

Source: Haemophilia. Mar2021, Vol. 27 Issue 2, p199-210. 12p. 3 Charts, 1 Graph.

Successful outcome of pregnancy post‐allogeneic stem cell transplant despite severe RH1 alloimmunization: A case report.

Authors: Gavillet, Mathilde Rufer, Nathalie Grandoni, Francesco et al.

Source: British Journal of Haematology. May2023, Vol. 201 Issue 3, p581-584. 4p.

La transfusion de CGR en néonatologie : pratiques transfusionnelles en Suisse.

Authors: Canellini, Giorgia Gavillet, Mathilde Fontana, Stefano et al.

Source: Transfusion Clinique et Biologique. Nov2025:Supplement, Vol. 32 Issue 4, pS9-S9. 1p.

T315I clone selection in a Ph+ all patient under low-dose ponatinib maintenance.

Authors: Noetzli, Jasmine Gavillet, Mathilde Masouridi‐Levrat, Stavroula et al.

Source: Clinical Case Reports. Aug2017, Vol. 5 Issue 8, p1320-1322. 3p.

A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family.

Authors: Voruz, Sophie Noetzli, Jasmine Gavillet, Mathilde et al.

Source: Haemophilia. Jan/Feb2026, Vol. 32 Issue 1, p344-347. 4p.

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Acute leukemia in the time of COVID-19.

Authors: Gavillet, Mathilde Carr Klappert, Jeanette Spertini, Olivier et al.

Source: Leukemia Research. May2020, Vol. 92, pN.PAG-N.PAG. 1p.

Haematological changes from conception to childbirth: An indicator of major pregnancy complications.

Authors: Patxot, Marion Stojanov, Miloš Ojavee, Sven Erik et al.

Source: European Journal of Haematology. Nov2022, Vol. 109 Issue 5, p566-575. 10p.

Pseudo‐macrocytosis in chronic lymphocytic leukaemia.

Authors: Costanza, Mariangela Coutaz, Christine Cairoli, Anne et al.

Source: International Journal of Laboratory Hematology. Oct2023, Vol. 45 Issue 5, p623-624. 2p.

Hémochromatose héréditaire, hyperferritinémie et qualité des CGR.

Authors: Infanti, Laura Prudent, Michel Martin, Agathe et al.

Source: Transfusion Clinique et Biologique. Nov2025:Supplement, Vol. 32 Issue 4, pS38-S38. 1p.

Loss of Function of TET2 Cooperates with Constitutively Active KIT in Murine and Human Models of Mastocytosis.

Authors: De Vita, Serena Schneider, Rebekka K. Garcia, Michael et al.

Source: PLoS ONE. May2014, Vol. 9 Issue 5, p1-13. 13p.

Pregnancy with Chuvash Polycythaemia and Other Congenital Erythrocytosis.

Authors: Dewarrat, Natacha Kaiser, Julie Baud, David et al.

Source: Acta Haematologica. 2020, Vol. 143 Issue 1, p69-72. 4p. 1 Chart, 1 Graph.

Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients.

Authors: Andolfo, Immacolata Martone, Stefania Rosato, Barbara Eleni et al.

Source: Genes. Jul2021, Vol. 12 Issue 7, p958. 1p.