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ICORD | International Conference on Rare Diseases and Orphan Drugs

ICORD is an International Society for all individuals actively involved in rare diseases and/or orphan drugs.

http://www.icord.se/

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ICORD | International Conference on Rare Diseases and Orphan Drugs | icord.se Reviews
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ICORD | International Conference on Rare Diseases and Orphan Drugs | icord.se Reviews

https://icord.se

ICORD is an International Society for all individuals actively involved in rare diseases and/or orphan drugs.

INTERNAL PAGES

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1

ICORD » Bank and payment information

http://icord.se/main-menu/bank_information

Society & Membership. Bank and payment information. Bank and payment information. Paying your membership fee. We accept VISA and MasterCard credit card. If you are not yet a member, please send in your membership application, go to Membership page. If you are already a member, please tick the Membership box in the online payment page. Should you experience problems with your credit card payment, please consult your bank. Make a payment order using the following bank information:. Bank name: Danske Bank.

2

ICORD » Aims

http://icord.se/main-menu/aims

Society & Membership. Bank and payment information. To organise International Conferences on Rare Diseases and Orphan Drugs (ICORD). To promote research, ethics, policies and actions on rare diseases and orphan products in all regions of the world. To facilitate and provide a global forum for all stakeholders for effective communication, formation of opinion and public debate, concerning rare diseases and orphan products. Return to Welcome start page. Updated: February 20, 2010.

3

ICORD » ICORD 2014 Ede

http://icord.se/past-events/icord-2014

Society & Membership. Bank and payment information. ICORD 2015 Mexico City. ICORD 2013 St Petersburg. Swedish Satellite Meeting 2005. IX Annual meeting of ICORD. The Societal value of Prevention, Diagnosis and Treatments of Rare Diseases. We also would like to thank the Dutch Medicines Day (FIGON DMD) and ZonMw who provided the opportunities to interact globally. The conference report summarizes the ICORD annual conference in Ede in 19 pages, including photos. VENUE, DATES AND PROGRAM. Domenica Taruscio,...

4

ICORD » Presentations ICORD 2014

http://icord.se/past-events/icord-2014/presentations-icord-2014

Society & Membership. Bank and payment information. ICORD 2015 Mexico City. ICORD 2013 St Petersburg. Swedish Satellite Meeting 2005. Opening and Plenary Lectures. Policies: The main steps for recognizing the societal value of diagnosis, prevention and treatment of rare diseases. Domenica Taruscio (ICORD Past-President, Italy). John Forman (ICORD President -. Elect, New Zeeland),. ICORD – a platform for bridging and cooperation. Virginia Llera (ICORD-President, Argentina. Yann Le Cam (EURORDIS, France).

5

ICORD » Society & Membership

http://icord.se/main-menu/society_and_membership

Society & Membership. Bank and payment information. Society & Membership. The ICORD (International Conferences for Rare Diseases and Orphan Drugs) Society was formed on September 13, 2007 in Brussels. Its mission is to improve the welfare of patients with rare diseases and their families world-wide through better knowledge, research, care, information, education and awareness. The ICORD Society arranges the annual ICORD Conferences. ICORD meeting in May, 2008. ICORD Membership Application Form.

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ICORD » Conferences

http://www.icord.info/main-menu/conferences

Society & Membership. Bank and payment information. ICORD arranges annual Conferences on Rare Diseases and Orphan Drugs in different parts of the world. ICORD annual meeting 2016. Cape Town (South Africa) October 19-22, 2016. ICORD 2015 Mexico City. ICORD 2014 Ede, The Netherlands. ACCORD workshop 2014 Stockholm. ICORD 2013 St Petersburg. ICORD 2012 in Tokyo. ICORD 2010 in Buenos Aires. ICORD 2009 in Rome. ICORD 2008 in Washington DC. ICORD 2007 in Brussels. ICORD 2006 in Madrid. ICORD 2005 in Stockholm.

icord.info icord.info

ICORD » Aims

http://www.icord.info/main-menu/aims

Society & Membership. Bank and payment information. To organise International Conferences on Rare Diseases and Orphan Drugs (ICORD). To promote research, ethics, policies and actions on rare diseases and orphan products in all regions of the world. To facilitate and provide a global forum for all stakeholders for effective communication, formation of opinion and public debate, concerning rare diseases and orphan products. Return to Welcome start page. Updated: February 20, 2010.

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Sällsynta diagnoser - sällsynt, inte ovanlig

http://sallsyntadiagnoser.gotlandica.se/Verksamhet/Samarbeten

Hoppa direkt till innehåll. Mål och stadgar ». Vår beskyddare ». Vårt 90-konto ». Fler databaser ». Regionala strukturer för brukarmedverkan ». Sällsynta dagen ». Undersökningar, kursmaterial och annat publicerat ». Medlemsskap i Sällsynta diagnoser ». Sunnerdahls Handikappfond ». Råd, tips, möteslokaler ». Information till medlemmar ». Regionala strukturer för brukarmedverkan ». Sällsynta dagen ». Undersökningar, kursmaterial och annat publicerat ». Sällsynta nyheter 2 2015, Patienten i centrum. Bedrive...

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Semana Global 2015 EERR en CDMX - Boletia

https://semanaer.boletia.com/en

Semana Global 2015 EERR en CDMX. This event is finished. Want to locale the organizer? Para descripción en Español, click aquí. The Global Week 2015 on Rare Diseases. GW2015RD) in Mexico City. Here are the five most important days to raise awareness about this complex issue of public health in Mexico. Oct 12 : : 4th Latin American Meeting for Rare Patients Advocates. Oct 13-14 : : Medical congress "Discoveries and Innovations on Orphan Drugs". Oct 14 : : Gala Dinner. La Semana Global 2015 sobre Enfermeda...

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Semana Global 2015 EERR en CDMX - Boletia

https://semanaer.boletia.com/es

Semana Global 2015 EERR en CDMX. Este evento ya ha terminado. Quieres localizar al organizador? Para descripción en Español, click aquí. The Global Week 2015 on Rare Diseases. GW2015RD) in Mexico City. Here are the five most important days to raise awareness about this complex issue of public health in Mexico. Oct 12 : : 4th Latin American Meeting for Rare Patients Advocates. Oct 13-14 : : Medical congress "Discoveries and Innovations on Orphan Drugs". Oct 14 : : Gala Dinner. La Semana Global 2015 sobre ...

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Semana Global 2015 EERR en CDMX - Boletia

https://semanaer.boletia.com/new-booking

Semana Global 2015 EERR en CDMX. Este evento ya ha terminado. Quieres localizar al organizador? Para descripción en Español, click aquí. The Global Week 2015 on Rare Diseases. GW2015RD) in Mexico City. Here are the five most important days to raise awareness about this complex issue of public health in Mexico. Oct 12 : : 4th Latin American Meeting for Rare Patients Advocates. Oct 13-14 : : Medical congress "Discoveries and Innovations on Orphan Drugs". Oct 14 : : Gala Dinner. La Semana Global 2015 sobre ...

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Fler aktörer : Sällsynta Diagnoser

http://www.sallsyntadiagnoser.se/verksamhet/samarbeten

Om oss Visa submeny. Om Riksförbundet Sällsynta diagnoser. Sällsynta dagen Visa submeny. Medlemskap i Sällsynta diagnoser. Det finns en rad aktörer som arbetar för personer som har sällsynta diagnoser. Här har vi listat de viktigaste. Och sex tredagarsvistelser för vuxna med sällsynta diagnoser. Nationella Funktionen för Sällsynta Diagnoser. Informationscentrum för ovanliga diagnoser. Är ett centrum vid Göteborgs universitet som arbetar för att öka medvetenheten och kunskapen om ovanliga sjukdomar och sy...

orphanet.se orphanet.se

Villkor för användning

http://www.orphanet.se/national/SE-SV/index/villkor-för-användning

Sveriges ingång till Orphanet. Få tillgång till Orphanets tjänster i Sverige och andra länder på:. Hitta på Orpha.net. 5 okt 2016: Klinefelter syndrom. 7 okt 2016: Barn och ungdomar med extremitetsavvikelser/dysmeli. 12 okt 2016: Sällsynta diagnoser - för handläggare inom LSS-verksamhet, socialtjänst, försäkringskassa och arbetsförmedling. 31 okt and 21 nov: Sällsynta diagnoser - Föräldraträff. ERS international congress 2016. 27th European Dysmorphology Meeting. Svensk Förening för Medicinsk Genetik.

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Om sällsynta diagnoser

http://www.orphanet.se/national/SE-SV/index/om-sällsynta-diagnoser

Sveriges ingång till Orphanet. Få tillgång till Orphanets tjänster i Sverige och andra länder på:. Hitta på Orpha.net. 5 okt 2016: Klinefelter syndrom. 7 okt 2016: Barn och ungdomar med extremitetsavvikelser/dysmeli. 12 okt 2016: Sällsynta diagnoser - för handläggare inom LSS-verksamhet, socialtjänst, försäkringskassa och arbetsförmedling. 31 okt and 21 nov: Sällsynta diagnoser - Föräldraträff. ERS international congress 2016. 27th European Dysmorphology Meeting. Svensk Förening för Medicinsk Genetik.

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