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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue 3-4
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Original Article

An Electronic Infrastructure for Research and Treatment of the Thalassemias and Other Hemoglobinopathies: The Euro-Mediterranean Ithanet Project

Carsten W. Lederer The Cyprus Institute of Neurology and Genetics, Nicosia, CyprusCorrespondence[email protected]
,
A. Nazli Basak Boğaziçi University, Istanbul, Turkey
,
Yesim Aydinok EGE University, Izmir, Turkey
,
Soteroula Christou Ministry of Health, Nicosia, Cyprus
,
Amal El-Beshlawy Cairo University, Cairo, Egypt
,
Androulla Eleftheriou Thalassaemia International Federation, Nicosia, Cyprus
,
Slaheddine Fattoum Hopital d'Enfants, Tunis, Tunisia
,
Alex E. Felice University of Malta, Msida, Malta
,
Eitan Fibach Hadassah Medical Organization, Jerusalem, Israel
,
Renzo Galanello University of Cagliari, Cagliari, Italy
,
Roberto Gambari Ferrara University, Ferrara, Italy
,
Lucian Gavrila University of Bucharest, Bucharest, Romania
,
Piero C. Giordano Leiden University Medical Center, Leiden, Netherlands
,
Frank Grosveld Erasmus University Medical Center, Rotterdam, Netherlands
,
Helen Hassapopoulou University General Hospital of Thessaloniki AHEPA, Thessaloniki, Greece
,
Eva Hladka CESNET, z.s.p.o., Prague, Czech Republic
,
Emmanuel Kanavakis National & Kapodistrian University of Athens, Athens, Greece
,
Franco Locatelli IRCCS Policlinico San Matteou, Pavia, Italy
,
John Old Oxford Radcliffe Hospitals National Health Service Trust, Oxford, Oxfordshire, UK
,
George P. Patrinos Asclepion Genetics Sàrl, Lausanne, Switzerland
,
Giovanni Romeo European Genetics Foundation, Bologna, Italy
,
Ali Taher The Chronic Care Center, Beirut, Lebanon
,
Joanne Traeger-Synodinos National & Kapodistrian University of Athens, Athens, Greece
,
Panayiotis Vassiliou The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus
,
Ana Villegas Hospital Clinico San Carlos, Madrid, Spain
,
Ersi Voskaridou Laikon General Hospital, Athens, Greece
,
Henri Wajcman Institut National de la Sante et de la Recherche Medicale, Créteil Cédex, France
,
Anastasios Zafeiropoulos Greek Research and Technology Network, Athens, Greece
&
Marina Kleanthous The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus
 show all
Pages 163-176 | Received 18 Mar 2009, Accepted 26 Mar 2009, Published online: 15 Sep 2009

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Nafis Muhimmatul ‘Ulya, Vera Nurohmah Indrawati, Woro Triaksiwi Wulansari, Indra Lesmana & Niken Satuti Nur Handayani. (2023) Mutation Spectrum of β-Globin Gene in Patients with β-Thalassemia at Tidar Hospital, Magelang, Central Java, Indonesia. Hemoglobin 47:4, pages 152-156.
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Manousos E. Kambouris. (2016) Population Screening for Hemoglobinopathy Profiling: Is the Development of a Microarray Worthwhile?. Hemoglobin 40:4, pages 240-246.
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Alessia Finotti, Laura Breda, Carsten W Lederer, Nicoletta Bianchi, Cristina Zuccato, Marina Kleanthous, Stefano Rivella & Roberto Gambari. (2015) Recent trends in the gene therapy of β-thalassemia. Journal of Blood Medicine 6, pages 69-85.
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Alessia Finotti & Roberto Gambari. (2014) Recent trends for novel options in experimental biological therapy of β-thalassemia. Expert Opinion on Biological Therapy 14:10, pages 1443-1454.
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Laura Breda, Stefano Rivella, Cristina Zuccato & Roberto Gambari. (2013) Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia. Expert Review of Hematology 6:3, pages 255-264.
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Roberto Gambari. (2012) Alternative options for DNA-based experimental therapy of β-thalassemia. Expert Opinion on Biological Therapy 12:4, pages 443-462.
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Articles from other publishers (12)

Syahzuwan Hassan, Rosnah Bahar, Muhammad Farid Johan, Ezzeddin Kamil Mohamed Hashim, Wan Zaidah Abdullah, Ezalia Esa, Faidatul Syazlin Abdul Hamid & Zefarina Zulkafli. (2023) Next-Generation Sequencing (NGS) and Third-Generation Sequencing (TGS) for the Diagnosis of Thalassemia. Diagnostics 13:3, pages 373.
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Maria Xenophontos, Anna Minaidou, Coralea Stephanou, Stella Tamana, Marina Kleanthous & Petros Kountouris. (2023) IthaPhen: An Interactive Database of Genotype-Phenotype Data for Hemoglobinopathies. HemaSphere 7:7, pages e922.
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Roberto Gambari & Marina Kleanthous. (2019) Theranostics of Genetic Diseases. Molecular Diagnosis & Therapy 23:2, pages 153-154.
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Houda Elloumi‐Zghal & Habiba Chaabouni Bouhamed. (2018) Genetics and genomic medicine in Tunisia. Molecular Genetics & Genomic Medicine 6:2, pages 134-159.
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Theodora Katsila & George P. Patrinos. 2018. Human Genome Informatics. Human Genome Informatics 91 107 .
Petros Kountouris, Ioanna Kousiappa, Thessalia Papasavva, George Christopoulos, Eleni Pavlou, Miranda Petrou, Xenia Feleki, Eleni Karitzie, Marios Phylactides, Pavlos Fanis, Carsten W. Lederer, Andreani R. Kyrri, Eleni Kalogerou, Christiana Makariou, Christiana Ioannou, Loukas Kythreotis, Georgia Hadjilambi, Nicoletta Andreou, Evangelia Pangalou, Irene Savvidou, Michael Angastiniotis, Michael Hadjigavriel, Maria Sitarou, Annita Kolnagou, Marina Kleanthous & Soteroula Christou. (2016) The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study. Scientific Reports 6:1.
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Mohsen Jahangirian & Simon J.E. Taylor. (2013) Profiling e-health projects in Africa: trends and funding patterns. Information Development 31:3, pages 199-218.
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Carsten W. Lederer, Eleni Pavlou, Christiana Makariou, Georgia Hadjilambi, Nicoletta Andreou, Michael Hadjigavriel, Annita Kolnagou, Maria Sitarou, Soteroulla Christou & Marina Kleanthous. (2014) Hb Famagusta—analysis of a novel δ-globin chain variant [HBD:c.60C>A] in four families with diverse globin genotypes. Annals of Hematology 93:9, pages 1625-1627.
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Petros Kountouris, Carsten W. Lederer, Pavlos Fanis, Xenia Feleki, John Old & Marina Kleanthous. (2014) IthaGenes: An Interactive Database for Haemoglobin Variations and Epidemiology. PLoS ONE 9:7, pages e103020.
Crossref
Thessalia E. Papasavva, Carsten W. Lederer, Jan Traeger‐Synodinos, Ariadne Mavrou, Emmanuel Kanavakis, Christiana Ioannou, Christiana Makariou & Marina Kleanthous. (2013) A Minimal Set of SNPs for the Noninvasive Prenatal Diagnosis of β ‐Thalassaemia . Annals of Human Genetics 77:2, pages 115-124.
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Alessia Finotti, Giulia Breveglieri, Monica Borgatti & Roberto Gambari. 2012. Detection of Non-Amplified Genomic DNA. Detection of Non-Amplified Genomic DNA 3 24 .
George P. Patrinos, Jumana Al Aama, Aida Al Aqeel, Fahd Al-Mulla, Joseph Borg, Andrew Devereux, Alex E. Felice, Finlay Macrae, Makia J. Marafie, Michael B. Petersen, Ming Qi, Rajkumar S. Ramesar, Joel Zlotogora & Richard G.H. Cotton. (2011) Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection. Human Mutation 32:1, pages 2-9.
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