Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ourania G. Papageorgiou"'
Autor:
Panagiotis Korovessis, Nicholas G. Beratis, Dimitris A. Papanastasiou, Alekos Oikonomopoulos, Ourania G. Papageorgiou
Publikováno v:
Pediatrics. 88:341-345
Skeletal abnormalities in patients with homozygous β thalassemia have been noted as early as 1927 by Cooley et al1 and have been the subject of many reviews.2-5 Abnormalities have been observed in the entire skeletal system, especially the skull and
Autor:
Jeane P. Hester, Mark J. Melaragno, Mari Nagata, Naoki Sadamori, Bertha A. Bouroncle, Christopher L. Reading, Takahiro Itoyama, Ourania G. Papageorgiou, Takeo Fujimoto, Naoyuki Katano, Dimitris A. Papanastasiou, A.E. Bradshaw, Hideo Nakamura, E. Fonseca, Lee Bairnsfather, A. Takatsuki, Keshava Prasad, Toshiro Hara, Masuko Tagawa, M. Sakaguchi, Y. Koishihara, Saroj Vadhan-Raj, Ruth Y. Wernli, Tammy R. Bordelon, Kanji Sakamoto, Luis Bello López, Seiji Tokunaga, F. Manso, Ronald G. Strauss, Yasunobu Yokoyama, M. Kawakita, Liisa Volin, William L. Marsh, Yoshitoshi Itoh, Keiji Sawada, Kohji Ueda, Karl S. Theil, Takaya Tanaka, Kuniaki Sasaki, G.J. Ventura, Micheal Bowen, Ei-ichi Yao, Ippei Sasagawa, Iris Th. Spiliopoulou, Nicholas G. Beratis, Hideki Kuriki, Kawai S, J. Matsushita, Tapani Ruutu, Isao Nakamura, Toshiaki Kamei, Hiroyuki Shimizu, Delores G. Cordle, Michito Ichimaru, Naoshi Takeyama, K. Shibuya, Tomoyuki Taniguchi, Glenn M. Mills, Robert E. Wolf, Daniel Sedmak, Bruce A. Baethge
Publikováno v:
Acta Haematologica. 84:I-IV
Autor:
Dimitris A. Papanastasiou, Iris Th. Spiliopoulou, Ourania G. Papageorgiou, Nicholas G. Beratis
Publikováno v:
Acta Haematologica. 84:182-185
The hepatitis B virus (HBV) markers have been studied in 184 household contacts of 110 thalassemic patients and 184 normal individuals matched for age and socioeconomic status with the study subjects. The mean age (+/- SD) in both patients and contro
Autor:
Michito Ichimaru, Jeane P. Hester, M. Sakaguchi, Glenn M. Mills, Takahiro Itoyama, Liisa Volin, Hideo Nakamura, Takaya Tanaka, Daniel Sedmak, Y. Koishihara, Lee Bairnsfather, Mark J. Melaragno, Yasunobu Yokoyama, Ei-ichi Yao, A.E. Bradshaw, Robert E. Wolf, Micheal Bowen, A. Takatsuki, Kawai S, E. Fonseca, Kuniaki Sasaki, Seiji Tokunaga, Delores G. Cordle, Naoyuki Katano, Dimitris A. Papanastasiou, Ourania G. Papageorgiou, Kohji Ueda, Luis Bello López, Masuko Tagawa, Toshiro Hara, Ippei Sasagawa, Tammy R. Bordelon, Saroj Vadhan-Raj, Kanji Sakamoto, Yoshitoshi Itoh, Ruth Y. Wernli, J. Matsushita, Tapani Ruutu, Isao Nakamura, Toshiaki Kamei, Keshava Prasad, F. Manso, Hideki Kuriki, Keiji Sawada, Christopher L. Reading, Naoki Sadamori, Naoshi Takeyama, G.J. Ventura, M. Kawakita, Bertha A. Bouroncle, William L. Marsh, Nicholas G. Beratis, Mari Nagata, Takeo Fujimoto, Ronald G. Strauss, Iris Th. Spiliopoulou, Tomoyuki Taniguchi, Bruce A. Baethge, Karl S. Theil, K. Shibuya, Hiroyuki Shimizu
Publikováno v:
Acta Haematologica. 84:219-220
Autor:
Nicholas G. Beratis, S. P. Gartaganis, Dimitris A. Papanastasiou, Ourania G. Papageorgiou, Konstantinos Ismiridis
Publikováno v:
American Journal of Ophthalmology. 108:699-703
We examined 29 patients with homozygous beta thalassemia. The mean age of the patients was 15.6 +/- 8.9 years. Twelve patients (mean age, 02.0 +/- 10.4 years) had one or more ocular abnormalities. Five patients had degeneration of the retinal pigment