Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ozsahin, Ayse Hulya"'
Autor:
Ansari Djaberi, Marc Georges, Strunk, Dirk, Schallmoser, Katharina, Delco, Cristina Maria, Rougemont-Pidoux, Anne-Laure, Moll, Solange, Villard, Jean, Gumy Pause, Fabienne, Chalandon, Yves, Parvex, Paloma Maria, Passweg, Jakob, Ozsahin, Ayse Hulya, Kindler, Vincent Lucien
Publikováno v:
Pediatric Transplantation, Vol. 16, No 2 (2012) pp. 131-6
TA-TMA is a pathology that occurs after allogenic HSC transplantation with an incidence of 4-13%, and represents one of the most severe vascular damage related with this therapy. We report here the case of a nine-yr-old girl suffering from a severe r
Autor:
Ozsahin, Ayse Hulya
Publikováno v:
Pediatric Blood and Cancer, Vol. 51, No 5 (2008) pp. 573-574
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1400::48890b2e9525c2fc15e4ecc74fe85fc8
https://archive-ouverte.unige.ch/unige:19203
https://archive-ouverte.unige.ch/unige:19203
Autor:
Seger, Reinhard A, Gungor, Tayfun, Belohradsky, Bernd H, Blanche, Stephane, Bordigoni, Pierre, Di Bartolomeo, Paolo, Flood, Terence, Landais, Paul, Müller, Susanna, Ozsahin, Ayse Hulya, Passwell, Justen H, Porta, Fulvio, Slavin, Shimon, Wulffraat, Nico, Zintl, Felix, Nagler, Arnon, Cant, Andrew, Fischer, Alain
Publikováno v:
Blood, Vol. 100, No 13 (2002) pp. 4344-50
Treatment of chronic granulomatous disease (CGD) with myeloablative bone marrow transplantation is considered risky. This study investigated complications and survival according to different risk factors present at transplantation. The outcomes of 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1400::adb10930b91e4609c89dfb0c23bb587d
https://archive-ouverte.unige.ch/unige:55904
https://archive-ouverte.unige.ch/unige:55904
Autor:
Girones, M, Aboun, G, Aubonney, S, Freudiger, T, Palama, F, De Sousa, L, Garcia, C, Dunant-Sauvin, C, Wacker, Pierre, Humbert, James Ronald, Ozsahin, Ayse Hulya
Publikováno v:
Journal for BMT Nursing, No 2 (1998) pp. 24-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1400::b4a75d438271863ad84dada027915c9e
https://archive-ouverte.unige.ch/unige:74599
https://archive-ouverte.unige.ch/unige:74599
Akademický článek
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Autor:
El Hassani, Yassine, Jenny, Benoit, Pittet-Cuenod, Brigitte, Bottani, Armand, Scolozzi, Paolo, Ozsahin Ayse, Hulya, Rilliet, Benédict
Publikováno v:
Child's Nervous System; Oct2013, Vol. 29 Issue 10, p1927-1931, 5p
Autor:
Campanelli, Alexandre, Kaya, Gürkan, Ozsahin, Ayse Hulya, La Scala, Giorgio, Jacquier, Cédric, Stauffer, Mélanie, Boehlen, Françoise, de Moerloose, Philippe, Saurat, Jean-Hilaire
Publikováno v:
Dermatology; March 2004, Vol. 208 Issue: 3 p262-264, 3p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Zsiros, József, Brugieres, Laurence, Brock, Penelope, Roebuck, Derek, Maibach, Rudolf, Zimmermann, Arthur, Childs, Margaret, Pariente, Daniele, Laithier, Veronique, Otte, Jean-Bernard, Branchereau, Sophie, Aronson, Daniel, Rangaswami, Arun, Ronghe, Milind, Casanova, Michela, Sullivan, Michael, Morland, Bruce, Czauderna, Piotr, Perilongo, Giorgio, International childhood liver tumours strategy group
Publikováno v:
The Lancet Oncology, Vol. 14, No 9 (2013) pp. 834-42
The Lancet Oncology
lancet oncology, 14(9), 834-842. Lancet Publishing Group
The Lancet Oncology
lancet oncology, 14(9), 834-842. Lancet Publishing Group
Summary Background The objective of this study was to establish the efficacy and safety of a new treatment regimen consisting of dose-dense cisplatin-based chemotherapy and radical surgery in children with high-risk hepatoblastoma. Methods SIOPEL-4 w
Autor:
George R. Buchanan, Leah Adix, Victor S. Blanchette, Sara K. Vesely, Cindy E. Neunert, Thomas Kühne, Paula H. B. Bolton-Maggs, Ellis J. Neufeld, Carolyn M. Bennett, Paul Imbach
Publikováno v:
Blood, Vol. 121, No 22 (2013) pp. 4457-62
Long-term follow-up of children with immune thrombocytopenia (ITP) indicates that the majority undergo remission and severe thrombocytopenia is infrequent. Details regarding bleeding manifestations, however, remain poorly categorized. We report here