thalassaemia.org.cy
Home page of the Thalassaemia International FederationThe home page of the International Federation for Thalassaemia and other Haemoglobin Disorders
http://thalassaemia.org.cy/
The home page of the International Federation for Thalassaemia and other Haemoglobin Disorders
http://thalassaemia.org.cy/
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Home page of the Thalassaemia International Federation | thalassaemia.org.cy Reviews
https://thalassaemia.org.cy
The home page of the International Federation for Thalassaemia and other Haemoglobin Disorders
Thalassaemia International Federation
http://thalassaemia.org.cy/patients-voice-and-involvement/testimonials.shtml
Phone: 357 22 319 129. Advocacy and Policy Issues. TIFs Mission, Vision, and Pillars. The Board of Directors. Awareness and Educational Programme. Country Work / Delegation Visits. Industry Circle / Sponsors. Sultan Bin Khalifa Award. We believe in give back! Congratulations to Thalassaemia Patient’s Friend Society (TPFS)! We are delighted to share with you some exciting news received from the Ministry of Heath of Palestine! Safe Blood Transfusion Programme Newsletter. UKTS Conference, 12 May 2016. We ar...
Thalassaemia International Federation
http://thalassaemia.org.cy/patients-voice-and-involvement/member-news.shtml
Phone: 357 22 319 129. Advocacy and Policy Issues. TIFs Mission, Vision, and Pillars. The Board of Directors. Awareness and Educational Programme. Country Work / Delegation Visits. Industry Circle / Sponsors. Sultan Bin Khalifa Award. We believe in give back! Congratulations to Thalassaemia Patient’s Friend Society (TPFS)! We are delighted to share with you some exciting news received from the Ministry of Heath of Palestine! Safe Blood Transfusion Programme Newsletter. UKTS Conference, 12 May 2016. We ar...
Thalassaemia International Federation
http://thalassaemia.org.cy/join_us.shtml
Phone: 357 22 319 129. Advocacy and Policy Issues. TIFs Mission, Vision, and Pillars. The Board of Directors. Awareness and Educational Programme. Country Work / Delegation Visits. Industry Circle / Sponsors. Sultan Bin Khalifa Award. We believe in give back! Congratulations to Thalassaemia Patient’s Friend Society (TPFS)! We are delighted to share with you some exciting news received from the Ministry of Heath of Palestine! Safe Blood Transfusion Programme Newsletter. UKTS Conference, 12 May 2016. We ar...
Thalassaemia International Federation
http://thalassaemia.org.cy/members-corner.shtml
Phone: 357 22 319 129. Advocacy and Policy Issues. TIFs Mission, Vision, and Pillars. The Board of Directors. Awareness and Educational Programme. Country Work / Delegation Visits. Industry Circle / Sponsors. Sultan Bin Khalifa Award. We believe in give back! Congratulations to Thalassaemia Patient’s Friend Society (TPFS)! We are delighted to share with you some exciting news received from the Ministry of Heath of Palestine! Safe Blood Transfusion Programme Newsletter. UKTS Conference, 12 May 2016. We ar...
- Thalassaemia International Federation
http://thalassaemia.org.cy/projects/video-sharing-platform-gallery.html
Phone: 357 22 319 129. Advocacy and Policy Issues. TIFs Mission, Vision, and Pillars. The Board of Directors. Awareness and Educational Programme. Country Work / Delegation Visits. Industry Circle / Sponsors. Sultan Bin Khalifa Award. We believe in give back! Awareness and Educational Programme. Country Work / Delegation Visits. Industry Circle / Sponsors. Sultan Bin Khalifa Award. Download TIF’s Digital Library. Download TIF’s ThaliMe application.
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12
Asia Pacific Iron Academy (APIA)-MRI Network
http://www.apia-mri.com/index.php
Asia Pacific Iron Academy (APIA)-MRI Network. Meetings & Symposiums. During Phase I of the APIA network,. All image analysis will initially be performed centrally at Mahidol University. The purpose of this is to ensure quality control across all of the network sites and provide the lowest barrier to participating centers. Meetings & Symposiums.
Abrasta - Talassemia - Notícias e Informações
http://www.abrasta.org.br/noticias-view?ID=280
Viver bem faz parte do tratamento. O que é Talassemia. Desafios para adesão ao Tratamento. Estudos e Casos Clínicos. Apoio à Equipe de Saúde. Resultados / Balanço Social. Reunião Ordinária do mês de Abril do Hospital HEMOPE. Encontre o local de tratamento e de transfusão mais próximo de você. Doe Sangue pela vida. Faça parte do nosso cadastro de doadores de sangue. Veja como e onde doar. Espaço para você interagir enviando perguntas ou opiniões. Confira a programação de todos os eventos e palestras.
Abrasta - Talassemia - Palavra do Presidente
http://www.abrasta.org.br/palavra-presidente-abrasta
Viver bem faz parte do tratamento. O que é Talassemia. Desafios para adesão ao Tratamento. Estudos e Casos Clínicos. Apoio à Equipe de Saúde. Resultados / Balanço Social. A Talassemia não representa uma limitação a nada daquilo que queremos fazer. Doe Sangue pela vida. Faça parte do nosso cadastro de doadores de sangue. Veja como e onde doar. Espaço para você interagir enviando perguntas ou opiniões. Abrasta é membro da.
Abrasta - Talassemia - Fale Conosco
http://www.abrasta.org.br/fale-conosco-abrasta
Viver bem faz parte do tratamento. O que é Talassemia. Desafios para adesão ao Tratamento. Estudos e Casos Clínicos. Apoio à Equipe de Saúde. Resultados / Balanço Social. Este é o seu canal direto com a Abrasta. Para solicitar maiores informações ou esclarecer dúvidas, basta preencher o formulário abaixo:. Escreva aqui a sua mensagem. Encontre o local de tratamento e de transfusão mais próximo de você. Doe Sangue pela vida. Faça parte do nosso cadastro de doadores de sangue. Veja como e onde doar.
Dr Niyaf's Thalassaemia Support Group: September 2005
http://niyafsthalgroup.blogspot.com/2005_09_01_archive.html
Dr Niyaf's Thalassaemia Support Group. A support network for people diagnosed with Beta Thalassaemia major, Thalassaemia carrier status, parents, guardians and family members of patients, medical professionals, paramedical personnel, administrators and managers of Thalassaemia services and anyone interested in Thalassaemia. Thursday, September 29, 2005. Interesting question: Iron tablets. Let me start by noting down some facts:. Iron does not cure Beta Thalassaemia! Through blood transfusions and by exce...
Dr Niyaf's Thalassaemia Support Group: August 2005
http://niyafsthalgroup.blogspot.com/2005_08_01_archive.html
Dr Niyaf's Thalassaemia Support Group. A support network for people diagnosed with Beta Thalassaemia major, Thalassaemia carrier status, parents, guardians and family members of patients, medical professionals, paramedical personnel, administrators and managers of Thalassaemia services and anyone interested in Thalassaemia. Tuesday, August 30, 2005. Alpha Thalassaemia in the Maldives. Prevention of thalassaemia and haemoglobinopathies in remote and isolated communities—The Maldives experience.
اليوم العالمي للدفاع المدني
http://www.jordan-id.net/international_thalassaemia_day.htm
أي ار / مايو. اليوم العالمي للثلاسيميا /. يحتفل العالم في الثامن من أي ار / مايو من كل عام باليوم العالمي للثلاسيميا. وقد جاء تحديد هذا اليوم لأول مرة عام 1994 تكريما لذكرى جورج إبن بانوس انجليزوس - رئيس الإتحاد العالمي للثلاسيميا - الذي توفي بمرض الثلاسيميا في الثامن من أي ار / مايو 1993، وكذلك تكريما لذكرى من توفي في هذا المرض ولمساندة المرضى الذين يعانون منه. أما عدد المصابين المسجلين فهو 1200 مريض من مختلف الأعمار. ويقدر عدد المواليد الجدد المصابين بالمرض في العام الواحد 70-80 مواطنا . يتوفون في مقتب...
Cacoethes Scribendi: May 2009
http://zyklon1985.blogspot.com/2009_05_01_archive.html
Thursday, May 28, 2009. The day of reckoning. I just found this. Yes, I shall take some time off from work and go someplace good to view it. A solar eclipse visible in your own country on your own birthday is not something to come by every day. Hmm maybe some latent magical powers shall surface. LOL. I have been reading The Strain by Guillermo del Toro. So don't blame me for having strange thoughts about solar eclipses. Links to this post. Sunday, May 17, 2009. Grey's Anatomy Season 5 Finale.
Cacoethes Scribendi: Where does my time go?
http://zyklon1985.blogspot.com/2009/04/where-does-my-time-go.html
Sunday, April 12, 2009. Where does my time go? Ok, there is alot and alot and alot of backdated posts that I wrote halfway and didn't complete. My time has been disappearing alot lately and I don't know where it goes. Anyway, I was in one of the pictures in The Star today. I myself didn't realize until someone told me about it. Then quite a number of people also began smsing me about it. Can you spot me? Anyway, updates and backdated posts coming soon. Lolof course. so obvious. Malacca, PJ, Malaysia.
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:::: Foundation Against Thalassaemia ::::
8220;Foundation Against Thalassaemia Regd.”. Is a registered NGO based at Faridabad Haryana India. Foundation was set up in 1995 and was registered under societies act 1860/21 on 24 April 2001 by a group of parents and charitable members of community. Shri Sudhanshu Ji Maharaj. Shri APJ Abdul Kalam. Ms Meena Juneja From Guntur, Andra Pradesh. Smt Shobha Tuli Thalassaemics India Delhi. Smt Tripta Sethi Past President Inner Wheel Club Qutab Delhi. Dr N K. Pandey. Ms Chitra Parihar Kidz Kingdom.
The domain name is registered
THE DOMAIN NAME IS REGISTERED. DOMÉNA JE ZAREGISTROVÁNA. A DOMAIN NÉV REGISZTRÁLT.
Thalassaemia Australia, Donate Blood
333 Waverley Rd Mt Waverley VIC 3149. Ph: 613 9888 2211 or EMAIL US. Cycle246').cycle({fx:'fade', timeout: 7200, speed: 9000});. Thalassaemia and related blood disorders. Genetic Testing and Counselling Services. Vision, Mission, Aims and Objectives. Why do you need TA? Beta Thalassaemia Minor - Carriers. Teacher resource for Students with Thalassaemia. Children receiving a blood transfusion. A membership supports Thalassaemia Australia's work. For more information go to our. Every little bit helps.
| Lab One Foundation of Thalassaemia
Lab One Foundation of Thalassaemia. LAB ONE FOUNDATION OF THALASSAEMIA. PROFILE OF FOUNDER CHAIRMAN. NEWS & EVENTS. HOW YOU CAN HELP. FIND A TREATMENT CENTRE. BECOME A TIF MEMBER. IMAGES & VIDEOS. Lab One Blood Donor Club. Lab One Foundation of Thalassaemia has started its journey from 1. Thalassaemia patients are getting special services from this hospital. All kinds of treatment facilities are available for Thalassaemia patients at Lab One Foundation of Thalassaemia. Lab One Foundation of Thalassaemia.
Home page of the Thalassaemia International Federation
And Our People ⇒. The Board of Directors. George Englezos and Panos Englezos Awards. Beta Thalassaemia ⇒. Other Forms of Thalassaemia and Abnormal Haemoglobins. The Cure of Thalassaemia. Alpha Thalassaemia ⇒. Sickle Cell Disease ⇒. Inheritance of Sickle Cell Disease. Cure of Sickle Cell Disease. Official European and Other Bodies. Other Disease and Disease Group Organisations. Professional Medical and Other Health Related Organisations and NGOs. International Network for Cardiology. Policy Issues ⇒.
Maldivian Thalassaemia Society
Maldivian Thalassaemia Society (MTS) is a non-governmental organization which came into existence in the year 1994 the sole purpose being to improve and enhance quality of lives of Thalassaemics in Maldives. With support from other parents, the co-founders Mohamed Moosa Didi and Mohamed Rasheed Ibrahim, both parents of Thalassaemic patients, founded this Society because of the urgent need for such an organization at that time.
Thalassaemia Society of Pakistan
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