Understanding Hashimoto's Encephalopathy 2016 Edition:
An Expanded and Updated Guide For Patients, Families, and Caregivers
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Autoimmune Encephalitis Studies

Autoimmune encephalitis: paving the way for early diagnosis
Jean-Christophe Antoine
The Lancet
Published Online: 19 February 2016
DOI: http://dx.doi.org/10.1016/S1474-4422(16)00025-9
Abstract: http://www.thelancet.com/journals/laneur/article/PIIS1474-4422(16)00025-9/fulltext
Clinical characterization of autoimmune LGI1 antibody limbic encephalitis
Gaoa, et al.
Science Direct
Available online 17 February 2016
doi:10.1016/j.yebeh.2015.12.041
Abstract: http://www.sciencedirect.com/science/article/pii/S1525505015006964
Cerebrospinal fluid markers of neuronal and glial cell damage to monitor disease activity and predict long-term outcome in patients with autoimmune encephalitis
Constantinescu, et al.
European Journal of Neurology
Article first published online: January 29th, 2016
DOI: 10.1111/ene.12942
Abstract: ttp://onlinelibrary.wiley.com/doi/10.1111/ene.12942/abstract;jsessionid=246D1558A96059C6B8BEB0D0A26C2C32.f04t03

Last updated by Web Team on March 5th, 2016

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AE Alliance
"The Autoimmune Encephalitis Alliance promotes collaboration to improve care, find a cure and create community so that no one faces autoimmune encephalitis alone.


The Encephalitis Society
"The Encephalitis Society is an International organization providing information and support for all causes of Encephalitis."


Encephalitis Global
"Encephalitis Global is a U.S.A. 501(c)(3) non-profit organization formed in 2005 as an alliance connecting encephalitis survivors and caregivers around the world."


Mark2Cure
Scientific literature is growing at a rate of more than 2 new articles every single minute. It is impossible for scientists to consume and understand the rapidly expanding ocean of biomedical literature. You can help biomedical researchers find the information they need to discover cures faster.


RareConnect.org
"Connecting Rare Disease Patients Globally"


RareDisesases.org
"Alone we are rare. Together we are strong.®"


Contact a Family
"For families with disabled children."


Madison's Foundation Provides information about rare diseases and connects parents whose children have the same rare disease.


NIH Health Hotline
Toll-free numbers from the National Library of Medicine's Health Hotlines Database.


HE Notebook - Wordpress Site
A great blog of an HE patient with a trove of information, personal stories, and links to medical studies.