Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 2
473
Views
57
CrossRef citations to date
0
Altmetric
Second Titus H.J. Huisman Memorial Symposium: Recent Advances in Hemoglobinopathy, May 8–9, 2006, Adana, Turkey

Results From The North Cyprus Thalassemia Prevention Program

Pages 257-264 | Published online: 07 Jul 2009

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (6)

Pustika A. Wahidiyat, Teny T. Sari, Ludi D. Rahmartani, Stephen D. Iskandar, Anastasia M. Pratanata, Ivana Yapiy, Iswari Setianingsih, Tubagus D. Atmakusuma & Anna M. Lubis. (2022) Thalassemia in Indonesia. Hemoglobin 46:1, pages 39-44.
Read now
Duran Canatan. (2014) Thalassemias and Hemoglobinopathies in Turkey. Hemoglobin 38:5, pages 305-307.
Read now
Mahmoud Hadipour Dehshal, Mehdi Tabrizi Namini, Alireza Ahmadvand, Mohsen Manshadi, Forouzan Sadeghian Varnosfaderani & Hassan Abolghasemi. (2014) Evaluation of the National Prevention Program in Iran, 2007–2009: the Accomplishments and Challenges with Reflections on the Path Ahead. Hemoglobin 38:3, pages 179-187.
Read now
Arslan Mirza, Alina Ghani, Anam Pal, Abeer Sami, Sana Hannan, Zohaib Ashraf, Sulala Iqbal, Umair Zafar Malik, Umar Hayat & Zafar Fatmi. (2013) Thalassemia and Premarital Screening: Potential for Implementation of a Screening Program Among Young People in Pakistan. Hemoglobin 37:2, pages 160-170.
Read now
Mahmoud Hadipour Dehshal, Alireza Ahmadvand, Sakineh Yousefi Darestani, Mohsen Manshadi & Hassan Abolghasemi. (2013) Secular Trends in the National and Provincial Births of New Thalassemia Cases in Iran From 2001 to 2006. Hemoglobin 37:2, pages 124-137.
Read now
Hossein Heli, Siamak Mirtorabi & Khashayar Karimian. (2011) Advances in iron chelation: an update. Expert Opinion on Therapeutic Patents 21:6, pages 819-856.
Read now

Articles from other publishers (51)

Teny Tjitra Sari, Ludi Dhyani Rahmartani, Angga Wirahmadi, Nathasha Brigitta Selene, Stephen Diah Iskandar & Pustika Amalia Wahidiyat. (2024) Psychological Burden among Pediatric Thalassemia Major Patients in Indonesia: A Review. Thalassemia Reports 14:2, pages 33-43.
Crossref
Шыхбаба оглы Бабаев Меджнун & Фирудин кызы Мамедова Рена. (2024) ПРОБЛЕМА ГЕМОГЛОБИНОПАТИЙ В МИРЕ И СОВРЕМЕННЫЕ МЕТОДЫ БОРЬБЫ С НИМИ. ПРОБЛЕМА ГЕМОГЛОБИНОПАТИЙ В МИРЕ И СОВРЕМЕННЫЕ МЕТОДЫ БОРЬБЫ С НИМИ.
Khaled M. Musallam, M. Domenica Cappellini, Thomas D. Coates, Kevin H.M. Kuo, Hanny Al-Samkari, Sujit Sheth, Vip Viprakasit & Ali T. Taher. (2024) Αlpha-thalassemia: A practical overview. Blood Reviews 64, pages 101165.
Crossref
Wanna Chetruengchai, Prasit Phowthongkum & Vorasuk Shotelersuk. (2024) Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais. BMC Medical Genomics 17:1.
Crossref
Aziz Suat Gunsel, Mahmut Cerkez Ergoren, Hatice Kemal, Haniyeh Rahbar Kafshboran, Levent Cerit, Ayla Turgay & Hamza Duygu. (2023) Determination of Carrier Frequency of Actionable Pathogenic Variants in Autosomal Recessive Genetic Diseases in the Turkish Cypriot Population. Genes 14:10, pages 1967.
Crossref
Khaled M. Musallam, Louise Lombard, Kristin D. Kistler, Maria Arregui, Keely S. Gilroy, Christina Chamberlain, Erin Zagadailov, Kimberly Ruiz & Ali T. Taher. (2023) Epidemiology of clinically significant forms of alpha‐ and beta‐thalassemia : A global map of evidence and gaps . American Journal of Hematology 98:9, pages 1436-1451.
Crossref
Ali Temelci, Hasan Güney Yılmaz, Gürkan Ünsal, Lokman Onur Uyanik, Dilek Yazman, Aysa Ayali & Giuseppe Minervini. (2023) Investigation of the Wetting Properties of Thalassemia Patients’ Blood Samples on Grade 5 Titanium Implant Surfaces: A Pilot Study. Biomimetics 8:1, pages 25.
Crossref
Muhammad Salman Khan, Azmat Ullah, Kaleem Nawaz Khan, Huma Riaz, Yasar Mehmood Yousafzai, Tawsifur Rahman, Muhammad E. H. Chowdhury & Saad Bin Abul Kashem. (2022) Deep Learning Assisted Automated Assessment of Thalassaemia from Haemoglobin Electrophoresis Images. Diagnostics 12:10, pages 2405.
Crossref
Ayesha Ahmad, Amrita Singh, Fareha Khatoon & Shweta Kumari. (2022) Assessing the Need for a Population-based Screening for Thalassemia in Pregnancy: Systematic Analysis of Evidence from Uttar Pradesh. Journal of South Asian Federation of Obstetrics and Gynaecology 14:2, pages 218-222.
Crossref
Bin Hashim Halim-Fikri, Carsten W. Lederer, Atif Amin Baig, Siti Nor Assyuhada Mat-Ghani, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Wardah Yusof, Diana Abdul Rashid, Nurul Fatihah Azman, Suthat Fucharoen, Ramdan Panigoro, Catherine Lynn T. Silao, Vip Viprakasit, Norunaluwar Jalil, Norafiza Mohd Yasin, Rosnah Bahar, Veena Selvaratnam, Norsarwany Mohamad, Nik Norliza Nik Hassan, Ezalia Esa, Amanda Krause, Helen Robinson, Julia Hasler, Coralea Stephanou, Raja-Zahratul-Azma Raja-Sabudin, Jacques Elion, Ghada El-Kamah, Domenico Coviello, Narazah Yusoff, Zarina Abdul Latiff, Chris Arnold, John Burn, Petros Kountouris, Marina Kleanthous, Raj Ramesar & Bin Alwi Zilfalil. (2022) Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries. Journal of Personalized Medicine 12:4, pages 552.
Crossref
Lucio Luzzatto & Julie Makani. (2022) Treating Rare Diseases in Africa: The Drugs Exist but the Need Is Unmet. Frontiers in Pharmacology 12.
Crossref
Esther Kisanga, Ritah Mutagonda, David T. Myemba, Belinda J. Njiro, Franklin Simon, Alphonce I. Marealle, Wigilya P. Mikomangwa, Manase Kilonzi, Godfrey Sambayi & George M. Bwire. (2021) Premarital genetic screening and care of Tanzanian children with sickle cell disease: a qualitative study on parents’ views and experiences. Journal of Community Genetics 12:4, pages 515-523.
Crossref
Najat Rouh AlDeen, Asmaa A Osman, Monira J Alhabashi, Rasha Al Khaldi, Hassan Alawadi, Maha K Alromh, Eiman G Alyafai & Nagihan Akbulut-Jeradi. (2021) The Prevalence of β-Thalassemia and Other Hemoglobinopathies in Kuwaiti Premarital Screening Program: An 11-Year Experience. Journal of Personalized Medicine 11:10, pages 980.
Crossref
Mahmut C. Ergoren, Sehime G. Temel, Gamze Mocan & Munis Dundar. (2021) The Story of a Ship Journey, Malaria, and the HBB Gene IVS-II-745 Mutation: Circassian Immigration to Cyprus. Global Medical Genetics 08:02, pages 069-071.
Crossref
Cindy-Lee Dennis, Flavia Marini, Jennifer Abbass Dick, Stephanie Atkinson, Jon Barrett, Rhonda Bell, Anick Berard, Howard Berger, Hillary K Brown, Evelyn Constantin, Deborah Da Costa, Andrea Feller, Astrid Guttmann, Magdalena Janus, K S Joseph, Peter Jüni, Sarah Kimmins, Nicole Letourneau, Patricia Li, Stephen Lye, Jonathon L Maguire, Stephen G Matthews, David Millar, Dragana Misita, Kellie Murphy, Anne Monique Nuyt, Deborah L O'Connor, Rulan Savita Parekh, Andrew Paterson, Martine Puts, Joel Ray, Paul Roumeliotis, Stephen Scherer, Daniel Sellen, Sonia Semenic, Prakesh S Shah, Graeme N Smith, Robyn Stremler, Peter Szatmari, Deanna Telnner, Kevin Thorpe, Mark S Tremblay, Simone Vigod, Mark Walker & Catherine Birken. (2021) Protocol for a randomised trial evaluating a preconception-early childhood telephone-based intervention with tailored e-health resources for women and their partners to optimise growth and development among children in Canada: a Healthy Life Trajectory Initiative (HeLTI Canada). BMJ Open 11:2, pages e046311.
Crossref
SyedSameer Aga, YaraAbdulaziz Alghamdi, AmalAbdullah Alghamdi & MuhammadAnwar Khan. (2021) Knowledge, awareness, and attitude of medical students concerning genetics and premarital screening. Journal of Nature and Science of Medicine 4:4, pages 356.
Crossref
Farjana Akther Noor, Nusrat Sultana, Golam Sarower Bhuyan, Md Tarikul Islam, Mohabbat Hossain, Suprovath Kumar Sarker, Khaleda Islam, Waqar Ahmed Khan, Mujahida Rahman, Syeda Kashfi Qadri, Hossain Uddin Shekhar, Firdausi Qadri, Syed Saleheen Qadri & Kaiissar Mannoor. (2020) Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population. Orphanet Journal of Rare Diseases 15:1.
Crossref
Nehama Cohen-Kfir, Miriam Ethel Bentwich, Andrew Kent, Nomy Dickman, Mary Tanus, Basem Higazi, Limor Kalfon, Mary Rudolf & Tzipora C. Falik-Zaccai. (2020) Challenges to effective and autonomous genetic testing and counseling for ethno-cultural minorities: a qualitative study. BMC Medical Ethics 21:1.
Crossref
Pustika Amalia Wahidiyat, Teny Tjitra Sari, Ludi Dhyani Rahmartani, Iswari Setianingsih, Stephen Diah Iskandar, Anastasia Michelle Pratanata, Ivana Yapiy, Mikhael Yosia & Fernando Tricta. (2020) An insight into Indonesian current thalassaemia care and challenges. ISBT Science Series 15:3, pages 334-341.
Crossref
Sujata Sinha, Tulika Seth, Roshan B. Colah & Alan H. Bittles. (2019) Haemoglobinopathies in India: estimates of blood requirements and treatment costs for the decade 2017–2026. Journal of Community Genetics 11:1, pages 39-45.
Crossref
Subarna Chakravorty & Moira C Dick. (2019) Antenatal screening for haemoglobinopathies: current status, barriers and ethics. British Journal of Haematology 187:4, pages 431-440.
Crossref
Gulten Tuncel & Mahmut Çerkez Ergören. (2019) Functional coding and non-coding variants in human BRCA1 gene and their use in genetic screening. Medical Oncology 36:8.
Crossref
Baroukh Maurice Assael & Giovanni Boniolo. 2019. Philosophical and Methodological Debates in Public Health. Philosophical and Methodological Debates in Public Health 149 161 .
Md Tarikul Islam, Suprovath Kumar Sarkar, Nusrat Sultana, Mst. Noorjahan Begum, Golam Sarower Bhuyan, Shezote Talukder, A. K. M. Muraduzzaman, Md Alauddin, Mohammad Sazzadul Islam, Pritha Promita Biswas, Aparna Biswas, Syeda Kashfi Qadri, Tahmina Shirin, Bilquis Banu, Salma Sadya, Manzoor Hussain, Golam Sarwardi, Waqar Ahmed Khan, Mohammad Abdul Mannan, Hossain Uddin Shekhar, Emran Kabir Chowdhury, Abu Ashfaqur Sajib, Sharif Akhteruzzaman, Syed Saleheen Qadri, Firdausi Qadri & Kaiissar Mannoor. (2018) High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genetics 19:1.
Crossref
Poonam TripathiRavindra KumarSarita Agarwal. (2018) Spectrum and hematological profile of hereditary anemia in North Indians: SGPGI experience. Intractable & Rare Diseases Research 7:4, pages 258-263.
Crossref
Angela N. Barrett, Ramasamy Saminathan & Mahesh Choolani. (2017) Thalassaemia screening and confirmation of carriers in parents. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 27-40.
Crossref
Eman S. Alsaeed, Ghada N. Farhat, Abdullah M. Assiri, Ziad Memish, Elawad M. Ahmed, Mohammad Y. Saeedi, Mishal F. Al-Dossary & Hisham Bashawri. (2017) Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011–2015. Journal of Epidemiology and Global Health 7:S1, pages S41.
Crossref
Andrew Turner, Jurgen Sasse & Aniko Varadi. (2016) Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR). BMC Medical Genetics 17:1.
Crossref
G. Crighton, E. Wood, R. Scarborough, P. J. Ho & D. Bowden. (2016) Haemoglobin disorders in Australia: where are we now and where will we be in the future?. Internal Medicine Journal 46:7, pages 770-779.
Crossref
Fazeela Waheed, Colleen Fisher, AwoNiyi Awofeso & David Stanley. (2016) Carrier screening for beta-thalassemia in the Maldives: perceptions of parents of affected children who did not take part in screening and its consequences. Journal of Community Genetics 7:3, pages 243-253.
Crossref
F. Ouali, H. Siala, A. Bibi, S. Hadj Fredj, B. Dakhlaoui, R. Othmani, F. Ouenniche, F. Zouari, B. Bouguerra, H. Rezigua, S. Fattoum & T. Messaoud. (2016) Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience. International Journal of Laboratory Hematology 38:3, pages 223-232.
Crossref
Sohni V Dean, Zohra S Lassi, Ayesha M Imam & Zulfiqar A Bhutta. (2014) Preconception care: promoting reproductive planning. Reproductive Health 11:S3.
Crossref
Omar A Al-Farsi, Yahya M Al-Farsi, Ishita Gupta, Allal Ouhtit, Khalil S Al-Farsi & Samir Al-Adawi. (2014) A study on knowledge, attitude, and practice towards premarital carrier screening among adults attending primary healthcare centers in a region in Oman. BMC Public Health 14:1.
Crossref
Jeremy LauranceSarah HendersonPeter J. HowittMariam MatarHanan Al KuwariSusan Edgman-LevitanAra Darzi. (2014) Patient Engagement: Four Case Studies That Highlight The Potential For Improved Health Outcomes And Reduced Costs. Health Affairs 33:9, pages 1627-1634.
Crossref
Muhammad Shariq, Bushra Moiz, Nazneen Zaidi, Waleed Bin Azhar, Waseem Iqbal, Aiyesha Humaira & Rab Nawaz Memon. (2014) Pre-marital screening for beta thalassaemia in Pakistan: an insight. Journal of Medical Screening 21:3, pages 163-164.
Crossref
J.O. Kaufmann, I.P.C. Krapels, B.T.J. Van Brussel, R.C. Zekveld-Vroon, J.C. Oosterwijk, F. van Erp, J. van Echtelt, P.J.G. Zwijnenburg, F. Petrij, E. Bakker & P.C. Giordano. (2014) After the Introduction into the National Newborn Screening Program: Who Is Receiving Genetic Counseling for Hemoglobinopathies in The Netherlands?. Public Health Genomics 17:1, pages 16-22.
Crossref
J. O. Kaufmann, J. W. Smit, W. Huisman, R. N. Idema, E. Bakker & P. C. Giordano. (2012) Basic haemoglobinopathy diagnostics in D utch laboratories; providing an informative test result . International Journal of Laboratory Hematology 35:4, pages 428-435.
Crossref
Vassilis Ladis, Markissia Karagiorga‐Lagana, Ioanna Tsatra & Giorgos Chouliaras. (2013) Thirty‐year experience in preventing haemoglobinopathies in G reece: achievements and potentials for optimisation . European Journal of Haematology 90:4, pages 313-322.
Crossref
Sylvia M. van der Pal, Nicole M. C. van Kesteren, Jacobus P. van Wouwe, Paula van Dommelen & Symone B. Detmar. (2013) The Attitudes and Intention to Participate in Hemoglobinopathy Carrier Screening in The Netherlands among Individuals from Turkish, Moroccan, and Surinamese Descent. Journal of Environmental and Public Health 2013, pages 1-8.
Crossref
Hanan Hamamy. (2013) Community genetic services in Arab countries. Middle East Journal of Medical Genetics 2:1, pages 6-10.
Crossref
G. T. Roche. 2013. Legal and Forensic Medicine. Legal and Forensic Medicine 1519 1533 .
N. Rahmioglu, H. Naci & J. Cylus. (2012) Improving health care services in Northern Cyprus: a call for research and action. The European Journal of Public Health 22:6, pages 754-755.
Crossref
Elizabeth Argent, Phillip Emder, Paul Monagle, David Mowat, Toni Petterson, Susan Russell, Rani Sachdev, Christine Stone & David S Ziegler. (2011) Australian Paediatric Surveillance Unit study of haemoglobinopathies in Australian children. Journal of Paediatrics and Child Health 48:4, pages 356-360.
Crossref
Judith O. Kaufmann, Gönül Demirel‐Güngör, Anke Selles, Cisca Hudig, Gerard Steen, Gabrielle Ponjee, Cas Holleboom, Liv M. Freeman, Joris Hendiks, Pierre Wijermans, Piero C. Giordano & Jean‐Louis Kerkhoffs. (2011) Feasibility of nonselective testing for hemoglobinopathies in early pregnancy in The Netherlands. Prenatal Diagnosis 31:13, pages 1259-1263.
Crossref
Nicole E Cousens, Clara L Gaff, Sylvia A Metcalfe & Martin B Delatycki. (2010) Carrier screening for Beta-thalassaemia: a review of international practice. European Journal of Human Genetics 18:10, pages 1077-1083.
Crossref
Jumana Y. Al-Aama. (2010) Attitudes towards mandatory national premarital screening for hereditary hemolytic disorders. Health Policy 97:1, pages 32-37.
Crossref
Nazan Savas, Ebru Turhan, Tacettin Inandi & Hasan Kaya. (2010) Hemoglobinopathy awareness among high school students in Antakya (Antioch), Turkey. International Journal of Hematology 91:3, pages 413-418.
Crossref
Piero C. Giordano. (2009) Prospective and retrospective primary prevention of Hemoglobinopathies in multiethnic societies. Clinical Biochemistry 42:18, pages 1757-1766.
Crossref
Dong‐Zhi Li. (2009) Premarital screening for thalassemia in mainland China. Prenatal Diagnosis 29:6, pages 637-638.
Crossref
Parag M. Tamhankar, Sarita Agarwal, Vandana Arya, Ravindra Kumar, U. R. Gupta & S. S. Agarwal. (2008) Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India. Prenatal Diagnosis 29:1, pages 83-88.
Crossref
M. C. Cornel. (2008) Dragerschapsscreening. Bijblijven 24:6, pages 28-33.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.