Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dickenmann, Martina"'
Autor:
Neziri, Alban Y., Dickenmann, Martina, Scaramozzino, Pasquale, Andersen, Ole K., Arendt-Nielsen, Lars, Dickenson, Anthony H., Curatolo, Michele
Publikováno v:
In Pain 2012 153(2):311-318
Autor:
Simeunovic, Helena, Dickenmann, Martina, Nabergoj, Mitja, Baldomero, Helen, Masouridi‐Levrat, Stavroula, Nair, Gayathri, Schanz, Urs, Passweg, Jacob, Rovo, Alicia, Chalandon, Yves, Rebmann, Ekaterina
Publikováno v:
EJHaem; Feb2023, Vol. 4 Issue 1, p262-265, 4p
Autor:
Jalowiec, Katarzyna A., Andres, Martin, Mansouri Taleghani, Behrouz, Musa, Albulena, Dickenmann, Martina, Angelillo-Scherrer, Anne, Rovó, Alicia, Kremer Hovinga, Johanna Anna
BACKGROUND Acquired hemophilia A is a rare autoimmune disease with clinically often significant bleeding diathesis resulting from circulating autoantibodies inhibiting coagulation factor VIII. Half of acquired hemophilia A cases are associated with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4c146078b33fd67b5081ba87f56bc60
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Helena Simeunovic, Martina Dickenmann, Mitja Nabergoj, Helen Baldomero, Stavroula Masouridi‐Levrat, Gayathri Nair, Urs Schanz, Jacob Passweg, Alicia Rovo, Yves Chalandon, Ekaterina Rebmann
Publikováno v:
Simeunovic, Helena; Dickenmann, Martina; Nabergoj, Mitja; Baldomero, Helen; Masouridi-Levrat, Stavroula; Nair, Gayathri; Schanz, Urs; Passweg, Jacob; Rovo, Alicia; Chalandon, Yves; Rebmann, Ekaterina (2022). Allogeneic hematopoietic stem cell transplantation in Hodgkin lymphoma in Switzerland, 20 years of experience: 2001–2020. eJHaem, 4(1), pp. 262-265. Wiley 10.1002/jha2.629
Despite the high cure rate with initial therapy, approximately 10% of Hodgkin lymphoma (HL) patients are refractory to initial treatment, and up to 30% of patients will relapse after achieving initial complete remission. Despite promising initial res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a12ec50566d1a8a0d6e2cd6f8053c5
Autor:
Martina Dickenmann, Albulena Musa, Martin Andres, Alicia Rovó, Anne Angelillo-Scherrer, Johanna A. Kremer Hovinga, Katarzyna Aleksandra Jalowiec, Behrouz Mansouri Taleghani
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-6 (2020)
Jalowiec, Katarzyna A.; Andres, Martin; Mansouri Taleghani, Behrouz; Musa, Albulena; Dickenmann, Martina; Angelillo-Scherrer, Anne; Rovó, Alicia; Kremer Hovinga, Johanna Anna (2020). Acquired hemophilia A and plasma cell neoplasms: a case report and review of the literature. Journal of medical case reports, 14(1), p. 206. BioMed Central 10.1186/s13256-020-02505-7
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-6 (2020)
Jalowiec, Katarzyna A.; Andres, Martin; Mansouri Taleghani, Behrouz; Musa, Albulena; Dickenmann, Martina; Angelillo-Scherrer, Anne; Rovó, Alicia; Kremer Hovinga, Johanna Anna (2020). Acquired hemophilia A and plasma cell neoplasms: a case report and review of the literature. Journal of medical case reports, 14(1), p. 206. BioMed Central 10.1186/s13256-020-02505-7
BackgroundAcquired hemophilia A is a rare autoimmune disease with clinically often significant bleeding diathesis resulting from circulating autoantibodies inhibiting coagulation factor VIII. Half of acquired hemophilia A cases are associated with an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b9e656021dee386d943bbd4d2be35d
http://europepmc.org/articles/PMC7596986
http://europepmc.org/articles/PMC7596986