Tag Archives: Genomics of Rare Diseases

SERBORDISinn & 2014 Golden Helix Symposium “Genomics of Rare Diseases”

SERBORDISinn & 2014 Golden Helix Symposium “Genomics of Rare Diseases” was one of the main dissemination and promotion activities of the FP7 REGPOT SERBORDISinn. In order to attract more participants from abroad, IMGGE organized the Symposium in collaboration with Golden Helix Foundation. The Symposium was under the auspices of Ministry of Education, Science and Technological Development Republic of Serbia, Genomic Medicine Alliance and RD-Connect, while Orphanet and Public Health Genomics were communication sponsors. The Symposium was accredited by the Serbian Health Council (No. A-1-1990/14) for continuous medical education with the aim to attract more medical doctors and biochemist. IMGGE provided a free booth for the National organization for rare diseases of Serbia (NORBS) thus enabling patients to actively participate in the Symposium.

Symposium was organized into four sessions that addressed following topics: Public Health of Rare Diseases, Genomics of Rare Diseases, Pharmacogenomics and Individualized Therapy and Rare Diseases in Balkan Countries. Over 39 international, Balkan and Serbian researchers with an expertise in the field of rare diseases were invited to give lectures, and 128 participants (molecular biologists, biochemist, medical doctors and representatives of the relevant governmental departments) from Serbia and Balkan region participated in the event.

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Media coverage: The event was announced and commented in Serbian broadcasting and printed media thus increasing mentions of IMGGE in public media.

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Press release:

http://www.b92.net/zdravlje/vesti.php?yyyy=2014&mm=10&nav_id=918413

http://www.rtv.rs/sr_lat/zivot/porodica/dok-je-beba-u-stomaku-genom-otkriva-uzrok-bolesti_532038.html

http://www.blic.rs/Vesti/Drustvo/507357/Dijagnostika-retkih-bolesti-u-Srbiji-od-januara

http://www.ekapija.com/website/sr/page/1009539/Dijagnostika-retkih-bolesti-o-tro%C5%A1ku-RFZO-od-januara-2015

http://www.infogo.biz/dijagnostika-retkih-bolesti-u-srbiji-od-januara-332155.html

http://vazdan.com/vijest/dijagnostika-retkih-bolesti-u-srbiji-od-januara/826348

http://www.novosti.rs/vesti/zivot_+.304.html:517369-Dok-je-beba-u-stomaku-genom-otkriva-od-cega-ce-bolovati

http://pregledvesti.com/sjajno-otkrice-dok-je-beba-u-stomaku-genom-otkriva-od-cega/

http://www.medias.rs/najnovije-vesti/dok-je-beba-u-stomaku-genom-otkriva-od-cega-ce-bolovati/

http://www.netkafa.net/2014/10/31/1381424/dok-je-beba-u-stomaku-genom-otkriva-od-cega-ce-bolovati

http://www.prelistavanje.rs/vest/prikazi/sjajno-otkrice-dok-je-beba-u-stomaku-genom-otkriva-od-cega-ce-bolovati/1095812

http://www.hranazasve.com/zdravlje/vesti.php

Symposium Genomics of Rare Diseases General information

GENOMICS OF RARE DISEASES
SERBORDISINN & GOLDEN HELIX SYMPOSIUM
31. October – 1. November 2014.

 SerbordissInn-GoldenHelix

Meeting venue: Hotel Tulip Inn Putnik, Belgrade, Serbia www.tulipinnputnikbelgrade.com

Participants of Genomics of Rare Diseases SERBORDISinn and GoldenHelix Symposium could benefit from reduced room price in the Tulip Inn Putnik Hotel. For beneficial price please contact hotel directly. Contact person is Milica Tošić: mtosic@tulipinnputnikbelgrade.com

Registration: You may register online via SERBORDISinn.rs or GoldenHelix.org


Participation is free of charge.

The Symposium is accredited by the Health Council of Serbia (A-1-1990/14) to provide continuing medical education for physicians and biochemists (for lecturers 11 CME credits, for participants 5 CME credits).

Download updated SCIENTIFIC PROGRAM of Genomics of Rare Diseases in PDF format.

Abstract information

Abstract submission is optional. However, all submitted abstracts will be at display during Symposium and the Award will be given to the Best Abstract.

The corresponding author of the Best Abstract will be notified by October 20th in order to prepare 10 minutes oral presentation that will be held on October 31st at 16:30 hours.

Preparing an abstract for submission:

Abstract title (up to 50 word), Authors, Authors’ Affiliations, Text (up to 350 words) and the corresponding author’s e-mail.

Presentation format (only posters):

Poster should not be bigger than 70 cm width and 90 cm high. You are expected to bring your poster to the registration desk on Friday, October 31st between 08:00-08:30. Posters will be available for viewing during coffee breaks and lunches on October 31st and November 1st. Posters will be removed on November 1st during lunch time (15:00 at the latest).

Upcoming Symposium: Genomics of Rare Diseases

October 30th – November 1st, 2014, Belgrade, Republic of Serbia

The Symposium Faculty consists of international renowned speakers from Europe, the US and Asia.

The meeting will highlight the implementation of genomics to elucidate the molecular etiology of rare diseases in Serbia and the surrounding countries, as part of the EC-funded SERBORDISinn project.

Lastly, the meeting will feature the 2014 Genomic Medicine Alliance – pUblic Health Genomics award, presented for the best abstract submitted for this meeting.

Registration will open in July 2014.

For more information, registration and abstract submission, please click here to visit Golden Helix web site.
Download SCIENTIFIC PROGRAM of Genomics of Rare Diseases of Genomics of Rare Diseases Symposium in PDF format.