Search Results - "Angastiniotis, M."

ICSH recommendations for the measurement of Haemoglobin A2 by STEPHENS, A. D., ANGASTINIOTIS, M., BAYSAL, E., CHAN, V., FUCHAROEN, S., GIORDANO, P. C., HOYER, J. D., MOSCA, A., WILD, B.

“…Summary Although DNA analysis is needed for characterization of the mutations that cause β‐thalassaemia, measurement of the Hb A2 is essential for the routine…”
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Quality of Life in Thalassemia by TELFER, P., CONSTANTINIDOU, G., ANDREOU, P., CHRISTOU, S., MODELL, B., ANGASTINIOTIS, M.

“…: Morbidity and mortality related to thalassemia have been reduced significantly with modern medical treatment, and quality of life (QOL) should now be…”
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ICSH recommendations for the measurement of Haemoglobin F by STEPHENS, A. D., ANGASTINIOTIS, M., BAYSAL, E., CHAN, V., DAVIS, B., FUCHAROEN, S., GIORDANO, P. C., HOYER, J. D., MOSCA, A., WILD, B.

“…Summary Measurement of the Haemoglobin F in red cell haemolysates is important in the diagnosis of δβ thalassaemia, hereditary persistence of fetal haemoglobin…”
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Preimplantation diagnosis and HLA typing for haemoglobin disorders by Kuliev, A, Rechitsky, S, Verlinsky, O, Tur-Kaspa, I, Kalakoutis, G, Angastiniotis, M, Verlinsky, Y

“…Haemoglobin disorders are among the most frequent indications for preimplantation genetic diagnosis (PGD), introduced as an important option to couples at risk…”
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Prevention and control of haemoglobinopathies by ANGASTINIOTIS, M, MODELL, B, ENGLEZOS, P, BOULYJENKOV, V

“…In many developing countries the haemoglobinopathies (thalassaemias and sickle-cell disorder) are so common that they provide a convenient model for working…”
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P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL by Coralea Stephanou, C, Petros Kountouris, P, Carsten W Lederer, C, Celeste Bento, C, Cornelis L Hartveld, C, Jan Traeger‐Synodinos, J, John S Waye, J, Zhiyu Peng, Z, Irene Fylaktou, I, Hashim Halim‐Fikri, H, Tamara T. Koopmann, T, Landry Nfonsam, L, Jun Sun, J, Franck Nzengu‐Lukusa, F, Michael Angastiniotis, M, Catherine Badens, C, Bertha Ibarra Cortes, B, Johan T. den Dunnen, J, Jacques Elion, J, Suthat Fucharoen, S, Kyriaki Michailidou, K, Thessalia Papasavva, T, Antonio Piga, A, Raj Ramesar, R, Swee Lay Thein, S, Léon Tshilolo, L, Zilfalil Bin Alwi, Z, Marina Kleanthous, M

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International network on endocrine complications in thalassaemia (I-CET): an opportunity to grow by De Sanctis, V, Soliman, A T, Angastiniotis, M, Eleftheriou, A, Kattamis, Ch, Karimi, M, El Kholy, M, Elsedfy, H, Yassin, Mohd Abdel Daem Mohd, El Awwa, A, Stoeva, I, Skordis, N, Raiola, G, Fiscina, B

“…Most of the endocrine complications in thalassaemia are attributable to iron overload which may be the result of economic circumstances (expense of the…”
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Preimplantation diagnosis of thalassemias by Kuliev, A, Rechitsky, S, Verlinsky, O, Ivakhnenko, V, Evsikov, S, Wolf, G, Angastiniotis, M, Georghiou, D, Kukharenko, V, Strom, C, Verlinsky, Y

“…Preimplantation genetic diagnosis (PGD) is an important option for couples at risk of having children with beta-globin mutations to avoid selective abortions…”
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Fertility in female patients with thalassemia by Skordis, N, Christou, S, Koliou, M, Pavlides, N, Angastiniotis, M

“…With recent therapeutic advances, thalassemic patients can now reach adulthood and attain reproductive capacity. Endocrine complications due to hemosiderosis…”
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Birth of healthy children after preimplantation diagnosis of thalassemias by Kuliev, A, Rechitsky, S, Verlinsky, O, Ivakhnenko, V, Cieslak, J, Evsikov, S, Wolf, G, Angastiniotis, M, Kalakoutis, G, Strom, C, Verlinsky, Y

“…Preimplantation genetic diagnosis (PGD) allows couples at risk of having children with thalassemia to ensure the healthy outcome of their pregnancy. Seventeen…”
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Bone pain in thalassaemia: assessment of DEXA and MRI findings by Angastiniotis, M, Pavlides, N, Aristidou, K, Kanakas, A, Yerakaris, M, Eracleous, E, Posporis, T

“…An increasing number of adult thalassaemics have been complaining of aches and pains of varying degrees of severity. In a minority the pains are debilitating…”
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alpha-Thalassaemia in the population of Cyprus by Baysal, E, Kleanthous, M, Bozkurt, G, Kyrri, A, Kalogirou, E, Angastiniotis, M, Ioannou, P, Huisman, T H

“…We have determined the alpha-thalassaemia (alpha-thal) determinants in 78 patients with Hb H disease from Cyprus; 25 were Turkish Cypriots and 53 were Greek…”
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The adolescent thalassemic. The complicant rebel by Angastiniotis, M

“…Chronic hereditary conditions are expected to have a strong influence on the psychosocial development of the adolescent. Thalassaemia major is the commonest of…”
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Genetic Services in Cyprus by Angastiniotis, M., Middleton, L.

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Hb Bart's Levels in Cord Blood and α-Thalassemia Mutations in Cyprus by Kyriacou, K., Kyrri, A., Kalogirou, E., Vasiliades, Ph, Angastiniotis, M., Ioannou, P. A., Kleanthous, M.

“…The purpose of this study was to examine the frequency of α-thalassemia in the population of Cyprus using cord blood samples. The levels of Hb Bart's were…”
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Alpha-thalassaemia prenatal diagnosis by two PCR-based methods by Kleanthous, M., Kyriacou, K., Kyrri, A., Kalogerou, E., Vassiliades, PH, Drousiotou, A., Kallikas, I., Ioannou, P., Angastiniotis, M.

“…In Cyprus all couples carrying α0‐thalassaemia mutations are detected in the course of the thalassaemia carrier screening program and prenatal diagnosis is…”
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Global Epidemiology of Hemoglobin Disorders by ANGASTINIOTIS, MICHAEL, MODELL, BERNADETTE

“…: Thalassemias and the hemoglobinopathies such as Hemoglobins S, C and E, are now a global problem. They have spread through migration from their native areas…”
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The beta-thalassaemia mutations in the population of Cyprus by Baysal, E, Indrak, K, Bozkurt, G, Berkalp, A, Aritkan, E, Old, J M, Ioannou, P, Angastiniotis, M, Droushiotou, A, Yüregir, G T

“…We have identified the beta-thalassaemia alleles in nearly all known Turkish Cypriot beta-thalassaemia homozygotes and in over 700 Greek Cypriot…”
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ICSH recommendations for the measurement of Haemoglobin A 2 by STEPHENS, A. D., ANGASTINIOTIS, M., BAYSAL, E., CHAN, V., FUCHAROEN, S., GIORDANO, P. C., HOYER, J. D., MOSCA, A., WILD, B.

“…Summary Although DNA analysis is needed for characterization of the mutations that cause β‐thalassaemia, measurement of the Hb A 2 is essential for the routine…”
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Improved survival in thalassemia major patients on switching from desferrioxamine to combined chelation therapy with desferrioxamine and deferiprone by Telfer, Paul T, Warburton, Fiona, Christou, Soteroula, Hadjigavriel, Michael, Sitarou, Maria, Kolnagou, Anita, Angastiniotis, Michael

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