Zobrazeno 1 - 10
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pro vyhledávání: '"N, Illum"'
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Publikováno v:
Acta Ophthalmologica Scandinavica. 79:370-373
Purpose: To report on the efficacy of systemic Interferon-alfa therapy in controlling the endothelial proliferation in expanding facial haemangiomas of infancy threatening the eye. Methods: The series comprised 9 subjects with facial haemangiomas of
Autor:
Y. Shigenaga, M. Harms, I. Masouyé, B. Didona, R. Happle, E. Svejgaard, T. Kanzaki, A. Fiedler, P. Elsner, C. Willa-Craps, J.-H. Saurat, L. Didierjean, J. Sayag, G. Dawn, R. Hoffmann, P.H. Itin, C. Gelmetti, H.C. Korting, I. Braide, I. Ikeda, H. Ogawa, P.A. Piletta, R. Schultheiss, M. Yoshioka, M.C. Koeppel, E. Frenk, M. Yamazaki, T. Ono, T. Hisa, C. Mazzanti, C. Angeli-Besson, J.-M. Geiger, T. Kageshita, M.-H. Schmid, T. Fukumitsu, A.J. Kanwar, U.-F. Haustein, S. Ullman, P. Fileccia, D. Hohl, M.A. Fernández-Pugnaire, S. Mizoguchi, C. Nishikawa, C.R. Çelebi, T. Hamada, N. Kürkçüoğlu, T. Hunziker, T. Gobello, L. Andrac, R. Ammann, D. Guggisberg, V. Delgado-Florencio, S. Dhar, K. Rosén, K. Unno, M. Yssing, S. Cambiaghi, T. Rufli, T. Horio, C. Remondat, G. Scarabelli, B. Vion, H. Yaguchi, G. Pistritto, H. Miyauchi, P. Jacquet, A.M. Calza, C. Bertrand, G. Burg, S.A. Buechner, T. Karlsmark, I. Katayama, C. Hansson, C. Schepis, T. Yamamoto, M. Pechère, F. Atzori, K. Nishioka, R. Cavalieri, R. Tsuboi, N. Illum, M. Takigawa, P. Nenoff, M. Papi, M. Siragusa, Y. Hirachi, M. Setoyama, L.R. Braathen, P. Blecher
Publikováno v:
Dermatology. 191:I-VI
Autor:
J Jones, N Illum, D J Anstee, SN Wickramasinghe, Joyce Poole, E Wiener, Brigitte Gardner, Philip A. Judson, Stephen Parsons
Publikováno v:
Blood. 83:860-868
We have used a panel of well-characterized monoclonal antibodies (MoAbs) to examine the blood cells of a patient with a novel form of congenital dyserythropoietic anemia (CDA) characterized by intra- erythroblastic and intra-erythrocytic membranous i
Publikováno v:
Blood. 81:1636-1640
A 10-year-old Danish girl with congenital anemia is described. At birth, she had severe anemia and erythroblastosis and was transfused a number of times during the first year. The need for transfusions has since declined steadily. Her reticulocyte co
Publikováno v:
Blood. 81:1636-1640
A 10-year-old Danish girl with congenital anemia is described. At birth, she had severe anemia and erythroblastosis and was transfused a number of times during the first year. The need for transfusions has since declined steadily. Her reticulocyte co
Publikováno v:
Scandinavian Journal of Immunology. 34:635-645
We have characterized CD4-CD8- double-negative (DN) alpha beta TCR+ T cells from a patient with immunodeficiency, lymphocytosis, lymphadenopathy, and hepatosplenomegaly. The majority of peripheral blood lymphocytes were DN alpha beta TCR+ T cells as
Publikováno v:
British Journal of Haematology. 79:322-330
Summary A hitherto undescribed form of congenital dyserythropoietic anaemia is reported. The patient was severely anaemic and hydropic at birth and is now 8 years old. She has a moderate normochromic normocytic anaemia, HbF level of 50%, reticulocyte
Akademický článek
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