Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eleni Kalogerou"'
Autor:
Loukas Kythreotis, Xenia Felekis, Barbara J. Wild, Andreani R Kyrri, Marina Kleanthous, Marios Phylactides, Eleni Kalogerou
Publikováno v:
Hemoglobin. 33:81-94
Cyprus, located at the eastern end of the Mediterranean region, has been a place of eastern and western civilizations, and the presence of various hemoglobin (Hb) variants can be considered a testimony to past colonizations of the island. In this stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3938c939979c996b9ece40b515a837e3
https://doi.org/10.1080/03630260902813502
https://doi.org/10.1080/03630260902813502
Autor:
Marios Phylactides, Marina Kleanthous, Ioannis Georgiou, Eleni Kalogerou, Eleni Pavlou, Andriani Kyrri, Christiana Makariou
Publikováno v:
Hemoglobin. 30:455-462
To help clarify the hematological picture of patients who may be positive for β- and δ-globin gene mutations, the following study was carried out. Our aim was to identify the δ-globin gene mutations found in the Greek Cypriot population, their fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29a801954d01cb555965bce12f372a56
https://doi.org/10.1080/03630260600868006
https://doi.org/10.1080/03630260600868006
Autor:
Michael Angastiniotis, Andriani Kyrri, Kyriacos Kyriacou, Marina Kleanthous, Anthi Drousiotou, Ph. Vassiliades, I. Kallikas, Panos Ioannou, Eleni Kalogerou
Publikováno v:
Prenatal Diagnosis. 21:413-417
In Cyprus all couples carrying α0-thalassaemia mutations are detected in the course of the thalassaemia carrier screening program and prenatal diagnosis is offered to all of them. Prenatal diagnosis for α-thalassaemia is routinely done by two indep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d901ceb6299b549bc235764bf86fbbb
https://doi.org/10.1002/pd.73
https://doi.org/10.1002/pd.73
Autor:
Anthi Drousiotou, Marina Kleanthous, Andreani R Kyrri, George Christopoulos, Sotiroulla Christou, Kyriakos Kyriakou, Marios Phylactides, Eleni Kalogerou, Xenia Felekis
Publikováno v:
Hemoglobin. 32(3)
We report two cases of compound heterozygote patients for the --(MED I) and Hb Agrinio [alpha29(B10)Le-->uPro (alpha2)] anomalies in two unrelated Greek Cypriot families. The first patient had a serious form of Hb H disease and died at the age of 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d3b3c2b7dcbd342487c42b6c5d9fcf3
https://pubmed.ncbi.nlm.nih.gov/18473239
https://pubmed.ncbi.nlm.nih.gov/18473239
Autor:
Eleni, Pavlou, Marios, Phylactides, Andriani, Kyrri, Eleni, Kalogerou, Christiana, Makariou, Ioannis, Georgiou, Marina, Kleanthous
Publikováno v:
Hemoglobin. 30(4)
To help clarify the hematological picture of patients who may be positive for beta- and delta-globin gene mutations, the following study was carried out. Our aim was to identify the delta-globin gene mutations found in the Greek Cypriot population, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23dcc5f63d19d0d2aff997e2d77f2010
https://pubmed.ncbi.nlm.nih.gov/16987800
https://pubmed.ncbi.nlm.nih.gov/16987800
Autor:
Antroulla Kyrri, Eleni Kalogerou, Marina Kleanthous, Christiana Makariou, Xenia Felekis, George Christopoulos, Dena Loizidou
Publikováno v:
Hemoglobin. 25(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93eb3fa08fcef4a885efa4e4bc26394
https://pubmed.ncbi.nlm.nih.gov/11791876
https://pubmed.ncbi.nlm.nih.gov/11791876
Autor:
Dena Loizidou, Andreani R Kyrri, Christina Makariou, Michael Angastiniotis, Marios Phylactides, Christina Ioannou, Eleni Kalogerou, Marina Kleanthous, Bernadette Modell, Petros Kountouris, Loukas Kythreotis
Publikováno v:
Hemoglobin
The first epidemiological study for thalassemia in Cyprus was performed by Fawdry in 1946. The study determined that the frequency of β-thalassemia (β-thal) carriers was around 18.0% and that of α(0)-thal carriers (individuals with both cis α-glo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a7b780c27a82fb78ae28f29c80dfcf
Autor:
Miranda Petrou, Soteroula Christou, Christiana Ioannou, Michael Angastiniotis, Annita Kolnagou, Loukas Kythreotis, George Christopoulos, Petros Kountouris, Georgia Hadjilambi, Xenia Feleki, Irene Savvidou, Christiana Makariou, Carsten W. Lederer, Thessalia Papasavva, Michael Hadjigavriel, Eleni Karitzie, Marina Kleanthous, Pavlos Fanis, Marios Phylactides, Andreani R Kyrri, Eleni Kalogerou, Eleni Pavlou, Ioanna Kousiappa, Evangelia Pangalou, Nicoletta Andreou, Maria Sitarou
Publikováno v:
Scientific Reports
Haemoglobinopathies are the most common monogenic diseases, posing a major public health challenge worldwide. Cyprus has one the highest prevalences of thalassaemia in the world and has been the first country to introduce a successful population-wide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bf45a1621e8ef9d05f99d514167c23b