Resources

RELX,

November 2023

In this episode of the "World We Want" podcast, Márcia Balisciano interviews Filip Neele, Lead Scientist at TNO in Utrecht, the Netherlands. They discuss carbon capture and storage (CCS) technology as a “key” in energy transition and its role in supporting global sustainability.
Image of front cover of Elsevier report The Power of Data in Advancing the SDGs
RELX
Access to information is critical in achieving the SDGs - empowering the public to make decisions, informing policy making and enabling effective implementation and monitoring. RELX businesses regularly produce and publish free to download reports and analytics that draw upon vast amounts of information and data in support of the SDGs. Explore some of the reports and tools developed to date.
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
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
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
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
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
Elsevier

Rare Disease Education:  PGAP3-Congenital Disorder of Glycosylation

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

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

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