Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Anna Karastaneva"'
Autor:
Anna Karastaneva, Paolo Gasparella, Sebastian Tschauner, Roman Crazzolara, Gabriele Kropshofer, Manfred Modl, Andreas Pfleger, Ante Burmas, Mirjam Pocivalnik, Raphael Ulreich, Werner Zenz, Wolfgang Schwinger, Besiana P. Beqo, Christian Urban, Emir Q. Haxhija, Herwig Lackner, Martin Benesch
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundDespite recent developments, the role of sirolimus in the heterogeneous spectrum of vascular anomalies is yet to be defined, in terms of indication, dosage, and therapy duration, recognizing both its potential and limitations.MethodsWe retr
Externí odkaz:
https://doaj.org/article/599941b5a1f14c7aa31464ca7a04aa07
Autor:
Alireza Basharkhah, Herwig Lackner, Anna Karastaneva, Marko Bergovec, Stephan Spendel, Christoph Castellani, Erich Sorantin, Martin Benesch, Bernadette Liegl-Atzwanger, Freyja-Maria Smolle-Jüttner, Christian Urban, Michael Höllwarth, Georg Singer, Holger Till
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Introduction: Ewing sarcomas of the chest wall, historically known as “Askin tumors” represent highly aggressive pediatric malignancies with a reported 5-year survival ranging only between 40 and 60% in most studies. Multimodal oncological treatm
Externí odkaz:
https://doaj.org/article/20d396bb64644f7dbc3ab653d96ffb99
Autor:
Wolfgang Schwinger, Christian Urban, Raphael Ulreich, Daniela Sperl, Anna Karastaneva, Volker Strenger, Herwig Lackner, Kaan Boztug, Michael H. Albert, Martin Benesch, Markus G. Seidel
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Early diagnosis of primary immunodeficiency disorders (PID) is vital and allows directed treatment, especially in syndromes with severe or profound combined immunodeficiency. In PID patients with perinatal CMV or other opportunistic, invasive infecti
Externí odkaz:
https://doaj.org/article/c5eb36eb4eb14ea896c109bcc3caa409
Publikováno v:
Case Reports in Medicine, Vol 2014 (2014)
Although bone marrow transplantation (BMT) from an HLA identical sibling is considered as treatment of choice in pediatric patients with severe aplastic anemia (SAA), a significant number of them experience graft failure (GF) after BMT. We report a c
Externí odkaz:
https://doaj.org/article/5d515522e908487db2a1122aac8e6318
Autor:
Ellen Heitzer, Axel Schlagenhauf, Irina Grigorow, Martin Benesch, Anna Karastaneva, Markus G. Seidel, Gerald Höfler, Karin Nebral, Christian Urban, Oskar A. Haas, Andreas Greinacher, Raghavendra Palankar, Michael R. Speicher, Herbert Juch, Marcel Baschin
Publikováno v:
Journal of Medical Genetics. 57:427-433
Background. The phenotypes of patients with the recently discovered, dominant, ETV6-linked leukaemia predisposition and familial thrombocytopenia syndrome are variable, and the exact mechanism of leukaemogenesis remains unclear.Patients and Methods.
Autor:
Anna Karastaneva, R. Marterer, Volker Strenger, Gregor Gorkiewicz, Ch. Urban, Markus G. Seidel, Markus Egger, Benno Kohlmaier, Andreas Trobisch, Herwig Lackner, S. Flaschberger, Martin Benesch, Daniela Sperl
Publikováno v:
Supportive Care in Cancer
A 5-year-old patient treated for acute lymphoblastic leukaemia (ALL) developed proven pulmonary invasive fungal disease (IFD) due to Actinomucor elegans. While completing ALL treatment according to AIEOP ALL protocol 2009 for further 15 months, antif
Publikováno v:
Journal of Clinical Immunology. 39:19-22
Autor:
Erich Sorantin, Christoph Castellani, Herwig Lackner, Freyja-Maria Smolle-Jüttner, Bernadette Liegl-Atzwanger, Stephan Spendel, Georg Singer, Alireza Basharkhah, Michael E. Höllwarth, Marko Bergovec, Martin Benesch, Christian Urban, Holger Till, Anna Karastaneva
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics, Vol 9 (2021)
Introduction: Ewing sarcomas of the chest wall, historically known as “Askin tumors” represent highly aggressive pediatric malignancies with a reported 5-year survival ranging only between 40 and 60% in most studies. Multimodal oncological treatm
Publikováno v:
Monatsschrift Kinderheilkunde. 165:772-779
Autoimmunerscheinungen gehoren zum Symptomspektrum primarer Immundefekte und -dysregulationserkrankungen (PID). Immunzytopenien treten am haufigsten bei B‑ oder T‑Zell-Defekten auf; Patienten mit PID haben ein gegenuber der Normalbevolkerung ca.
Autor:
Anna, Karastaneva, Karin, Nebral, Axel, Schlagenhauf, Marcel, Baschin, Raghavendra, Palankar, Herbert, Juch, Ellen, Heitzer, Michael R, Speicher, Gerald, Höfler, Irina, Grigorow, Christian, Urban, Martin, Benesch, Andreas, Greinacher, Oskar A, Haas, Markus G, Seidel
Publikováno v:
Journal of medical genetics. 57(6)