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6 days ago
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2 weeks ago
Rare Disease Day, 29 Feb 2012 - Official Video
February 29, 2012 marks the fifth international Rare Disease Day coordinated by EURORDIS and organised with rare disease national alliances in 25 E...
rarediseaseday • 42,326 views
BLACKSWANFoundation
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3 months ago
Printing the BLACKSWAN Foundation's Brochure
This video present the printing of the BLACKSWAN Foundation Brochure. The process used is unique and completely innovative.
The random hand mixin...
930 views
BLACKSWANFoundation
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3 months ago
BLACKSWANFoundation
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1 year ago
BLACKSWANFoundation
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9 months ago
Flashmob Shary-An, Wiep & Natascha, Amsterdam
Genzyme has a shared commitment with the worldwide rare disease community: to raise the awareness of rare diseases.
On May 15th 2011 the Dutch Rar...
GenzymeEurope • 15,694 views
BLACKSWANFoundation
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9 months ago
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1 year ago
TEDxGeneva - Demian Conrad - Visualisation Of Rarity
TEDxGeneva -- Demian Conrad
Visualisation Of Rarity
Demian Conrad is the founder and creative director of the studio DEMIAN CONRAD DESIGN. Born i...
TEDxTalks • 883 views
BLACKSWANFoundation
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1 year ago
BLACKSWANFoundation
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1 year ago
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1 year ago
Marco Vignale's rare disorder
Myofibrillar Myopathy (MFM) refers to a genetically heterogeneous group of adult onset disorders sharing a homogeneous morphological pattern. Unlik...
rarediseaseday • 7 views
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1 year ago
Interview Olivier Menzel (President and Founder BLACKSWAN Foundation) English subtitles
The BLACKSWAN Foundation is a Swiss foundation supporting research for rare and orphan diseases.
Current international policy has poor public fund...
55 views
BLACKSWANFoundation
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1 year ago
VISUALIZATION OF RARITY (English subtitles)
BLACKSWAN is a Swiss Foundation keen on supporting the research of rare (Orphan) diseases, which directly affect more than 600 million people world...
42 views
BLACKSWANFoundation
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1 year ago
French Interview Olivier Menzel (President and Founder BLACKSWAN Foundation)
The BLACKSWAN Foundation is a Swiss foundation supporting research for rare and orphan diseases.
Current international policy has poor public fund...
95 views
BLACKSWANFoundation
uploaded
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1 year ago
VISUALIZATION OF RARITY (French)
BLACKSWAN is a Swiss Foundation keen on supporting the research of rare (Orphan) diseases, which directly affect more than 600 million people world...
296 views
BLACKSWANFoundation
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1 year ago
Children with Rare Disease (Phil. Society for Orphan Disorders Inc.)
The Philippine Society for Orphan Disorders, Inc. (PSOD) serves as a central network for the advocacy and effective coordination of all viable eff...
psod2006 • 6,916 views
BLACKSWANFoundation
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1 year ago
Printing the BLACKSWAN Foundation's Brochure (short version)
This video present the printing of the BLACKSWAN Foundation Brochure. The process used is unique and completely innovative.
The random hand mixin...
134 views
BLACKSWANFoundation
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1 year ago
BLACKSWANFoundation
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1 year ago
Prof. Thomas Cerny
Head of Oncology, Kantonsspital of St. Gallen and President of the Swiss Cancer League
mondobiotechrare • 113 views
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1 year ago
VOTE to help fund hope for sick kids Metro video
Text to 73774 (PEPSI). Followed by our voting code (102614) in the text message. Please vote daily, every vote counts. Voting ends September 30th.
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TheProjectCRDN • 292 views
BLACKSWANFoundation
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1 year ago
VOTE to help fund hope for sick kids I Hope video
Text to 73774 (PEPSI). Followed by our voting code (102614) in the text message. Please vote daily, every vote counts. Voting ends September 30th.
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TheProjectCRDN • 666 views
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1 year ago
About BLACKSWAN FOUNDATION
Created by
BLACKSWANFoundationLatest Activity
Feb 24, 2012Date Joined
Feb 27, 2010About this user
Swiss Foundation for Research on Orphan DiseasesFondazione Svizzera per la Ricerca sulle Malattie Orfane
Fondation Suisse pour la Recherche sur les Maladies Orphelines
Schweizer Stiftung für die Forschung an Seltenen Krankheiten
@sandrobtn001 slightly opaque white ink...