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Information maladies rares/Information rare diseases

11 Pins
 2y
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Regroupement québécois des maladies orphelines
#JournéeInternationale #handicap #sensibilisation #Hoptoys #Poster #Handicap Les gens rient parce que je suis différents, je ris parce qu'ils sont tous pareils. #différence Startup Weekend, International Day, Marketing Data, Aspergers, Occupational Therapy, Pathology, Cognitive, Acceptance, Sentimental
Startup Weekend
International Day
Marketing Data
Aspergers
Occupational Therapy
Pathology
Cognitive
Acceptance
Sentimental
#JournéeInternationale #handicap #sensibilisation #Hoptoys #Poster #Handicap Les gens rient parce que je suis différents, je ris parce qu'ils sont tous pareils. #différence
Hop'Toys
Hop'Toys
Information maladies rares/Information rare diseases
Check Rare Diseases and Symptoms - Checkrare.com Rare Disease, Genetics, Symptoms, Clinic, Insight, Check
Rare Disease
Genetics
Symptoms
Clinic
Insight
Check
Check Rare Diseases and Symptoms - Checkrare.com
Rare Disease Information and Resource Centre Support Telephone, Centre, Resources
Support Telephone
Centre
Resources
Rare Disease Information and Resource Centre
Centre d’information et de ressources en maladies rares Information
Information
Centre d’information et de ressources en maladies rares
[Full text] The health and life path of rare disease patients: results of the 2015 | PROM Peer Review, Life Path, Medical Care, The Professional, Psychology, Prom, Text, Luxury
Peer Review
Life Path
Medical Care
The Professional
Psychology
Prom
Text
Luxury
[Full text] The health and life path of rare disease patients: results of the 2015 | PROM
About GARD | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program Information Center, Medical Information, Leiden, Síndrome De Ehlers Danlos, Bartter Syndrome, Essential Thrombocythemia, Idiopathic Hypersomnia, Williams Syndrome, Mast Cell Activation Syndrome
Information Center
Medical Information
Leiden
Síndrome De Ehlers Danlos
Bartter Syndrome
Essential Thrombocythemia
Idiopathic Hypersomnia
Williams Syndrome
Mast Cell Activation Syndrome
About GARD | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
Orphanet Français France, Index, Drugs, English, Orphan, English Language, French
France
Index
Drugs
English
Orphan
English Language
French
Orphanet Français
Orphanet English
Orphanet English
Rare Diseases on the Internet: An Assessment of the Quality of Online Information Assessment, Knowledge, Internet, Health, Quality, Health Care, Business Valuation
Assessment
Knowledge
Internet
Health
Quality
Health Care
Business Valuation
Rare Diseases on the Internet: An Assessment of the Quality of Online Information
Rare Disease Information and Resource Centre – RQMO
Rare Disease Information and Resource Centre – RQMO
Centre d'information et de ressources en maladies rares
Centre d'information et de ressources en maladies rares