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| Poster session 1: Anemia - Congenital |
| Date: | Friday, June 11 2004 |
| Time: | 17:00-18:30 |
| Room: | |
| 17:00-18:30 |
239 |
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HAPLOTYPES LINKED TO THE BETA S GENE IN SICKLE CELL ANEMIA PATIENTS FROM SOUTHERN IRAN
Z. Rahimi, A. Merat, M. Haghshenass, N. Gerard, R. Krishnamoorthy, R.L. Nagel (Kermanshah, Iran)
| 17:00-18:30 |
240 |
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MICROANGIOPATHIC HAEMOLYTIC ANAEMIA IN SICKLE CELL DISEASE
D.K. Shome, A. Al Ajmi, F. Ali Darwish, K. Ravishekhar, A. Zaman, N. Malik (Manama, Bahrain)
| 17:00-18:30 |
241 |
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XMN I SITE POLYMORPHISM 5' TO GAMA G IN SICKLE CELL DISEASE IN SOUTHERN IRAN
Z. Rahimi, A. Merat, M. Haghshenass, M. Karimi, N. Gerard, R. Krishnamoorthy, R.L. Nagel (Kermanshah, Iran)
| 17:00-18:30 |
242 |
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A NEW VARIANT OF GLUCOSE PHOSPHATE ISOMERASE (GPI) (G145C/C921A) ASSOCIATED WITH SEVERE HEMOLYTIC ANEMIA
E. Fermo, C. Vercellati, P. Bianchi, M.G. Mariani, A. Marcello, A. De Fanti, G. Izzi, A. Zanella (Milan, Italy)
| 17:00-18:30 |
243 |
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DIAGNOSTIC AND ANEMIA-ASSOCIATED ABERRATIONS OF RED BLOOD CELL MEMBRANE PROTEINS IN HEREDITARY SPHEROCYTOSIS AND MILD THALASSEMIA
M.H. Antonelou, I.S. Papassideri, F.J. Karababa, A. Loutradi, L.H. Margaritis (Athens, Greece)
| 17:00-18:30 |
244 |
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IMPAIRED PROLIFERATION AND TRANSLATION IN DIAMOND-BLACKFAN ANEMIA PATIENTS
J.C. Cmejlova, L. Dolezalova, D. Pospisilova, R. Cmejla (Prague, Czech Republic)
| 17:00-18:30 |
245 |
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CHARACTERIZATION OF A PYRIMIDIN 5' NUCLEOTIDASE MUTANT FORM (G241R) CAUSING HEREDITARY HEMOLYTIC ANEMIA.
L.R. Chiarelli, A. Mattevi, A. Galizzi, P. Iadarola, E. Fermo, P. Bianchi, A. Zanella, G. Valentini (Pavia, Italy)
| 17:00-18:30 |
246 |
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THE EFFCT OF PROLACTIN ON THE PROLIFERATION AND DIFFERENTIATION OF ERYTHROID PROGENITORS FROM HEMATOPOIETIC STEM CELLS IN DIAMOND-BLACKFAN ANEMIA.
H. Kawasaki, Y. Noda, T. Nakano, Y. Kobayashi, K. Tsuji (Tokyo, Japan)
| 17:00-18:30 |
247 |
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A FAMILY WITH SECONDARY AND CONGENITAL POLYCYTHEMIA: PROBABLE INVOLVEMENT OF O2 SENSOR PATHWAY
J. del Río Garma, L. Kun, R. Kralovics, R. Skoda (Ribeira-la Coruña, Spain)
| 17:00-18:30 |
248 |
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THE FREQUENCY AND MOLECULAR GENETICS OF ERYTHROCYE G6PD DEFICIENCY IN ZANJAN CITY (NORTHWEST IRAN)
Y. Mortazavi, A.R. Esmaeilzadeh, S. Kalantari (Zanjan, Iran)
| 17:00-18:30 |
249 |
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MOLECULAR ANALYSIS OF FERROCHELATASE GENE IN ITALIAN PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA
M.D. Cappellini, E. Di Pierro, V. Moriondo, L. Perego, D. Tavazzi, P. Bonara (Milano, Italy)
| 17:00-18:30 |
250 |
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DIAGNOSTIC TOOLS IN CRYOHYDROCYTOSIS DEMONSTRATED IN A PATIENT WITH A SPONTANEOUS MUTATION
J.S. Goede, G.W. Stewart, R. Rüegg, J. Fehr, H.U. Lutz (Zürich, Switzerland)
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