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LexisNexis Risk Solutions
UGAHacks is a 501 (c)(3) non-profit organization that has been hosting an annual 48-hour hackathon for almost a decade now. This was the 2nd time HPCC Systems sponsored a challenge and participated in the hackathon held at the University of Georgia. If you want to catch up on our participation in last year’s event, please read the blog: UGA Hacks 8, Hot Wings and Hope for the Future.
Brown-Sequard Syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Brown-Sequard Syndrome
Elsevier

Rare Disease Education:  PGAP3-Congenital Disorder of Glycosylation

Editor: Kelsey LaFayette, DNP, RN, FNP-C

Reiter Syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Reiter Syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Autoimmune Polyglandular Syndrome Type I
Canavan Disease
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Canavan Disease
Shwachman-Diamond Syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Shwachman-Diamond Syndrome
Thoracic Outlet Syndrome
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Thoracic Outlet Syndrome
Fibromuscular Dysplasia
Elsevier
This article relates to SDG 3. This resource, created together by Osmosis and the National Organization for Rare Diseases (NORD), aims to increase the knowledge and awareness about Rare Disease Education: Fibromuscular Dysplasia

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