10 principais alextlc.org concorrentes

aldconnect.org

Please join ALD Connect for a discussion about ALD events, programs, projects, and initiatives at a Patient-Led Planning Committee meeting. This meeting, also known as Workgroup 4, is a place … Continued

alexanderdisease.com

Learn how the toxic accumulation of pathogenic variants of GFAP is one of the potential mechanisms responsible for Alexander disease.

mndaustralia.org.au

mnd australia is the national peak body supporting people impacted by motor neurone disease. we fund research to find treatments & ultimately a cure.

multiplesklerose.ch

Im Rahmen des Charity Games gegen den HC Davos engagierte sich der EHC Kloten erneut für Menschen mit Multipler Sklerose. Wir sagen Danke: Club, Spielern, Fans und allen Helfenden, die solche Spiele möglich machen.

alsjapan.org

ALS患者・家族の支援団体

youngepilepsy.org.uk

Needs editing - currenlty St Piers page

lewybody.org

We have put together the answers to some of the questions we get asked most often about Lewy body dementia.

uniliitto.fi

Uniliitto toimii unen häiriöihin ja hoitoon liittyvien rekisteröityjen yhdistysten yhteen liittävänä keskusjärjestönä. Tarjoamme unihäiriöistä kärsiville apua, tukea ja tietoa sekä edistämme edunvalvonnalla unihäiriöiden hoidon kehittämistä ja tasavertaista saavutettavuutta.

canfasd.ca

The Canada Fetal Alcohol Spectrum Disorder Research Network (CanFASD) is a collaborative, interdisciplinary research network, with collaborators, researchers and partners across the nation. It is Canada’s first comprehensive national Fetal Alcohol Spectrum Disorder (FASD) research network. It started as an alliance of seven jurisdictions and operated for seven years as the Canada Northwest FASD Research Network.

neurological.org.nz

Huntington’s disease is an inherited brain disorder that causes cells in specific parts of the brain to die which results in impairment of both mental capability and physical control. It is a genetic disorder caused by an expanded gene. While everybody has the gene, those who develop the disease have a longer version of the gene.