NTSAD Research Library
Explore Scientific Literature and Other Resources on Tay-Sachs, Canavan, GM1 gangliosidosis, and Sandhoff Diseases.
Over the years, National Tay-Sachs & Allied Diseases (NTSAD) has curated a collection of scientific literature and other resources on Tay-Sachs, Canavan, GM1 gangliosidosis, and Sandhoff diseases.
We’ll continue to add to this library so you can stay up to date on developments in the field.
You can search the NTSAD research library for:
- Scientific articles and posters
- NTSAD newsletters
- Advocacy information and toolkits
- Care guides
- Position statements
The pathogenesis of, and pharmacological treatment for, Canavan disease
1 file(s) 7 downloads
|Canavan Disease||May 27, 2022||Download|
The natural history of Canavan disease: 23 new cases and comparison with patients from literature.
1 file(s) 1 download
|Canavan Disease||May 19, 2021||Download|
Canavan Disease as a Model for Gene Therapy-Mediated Myelin Repair.
1 file(s) 62 downloads
|Canavan Disease||April 23, 2021||Download|
Gene Therapy for the Treatment of Neurological Disorders: Metabolic Disorders.
1 file(s) 3 downloads
|Canavan Disease||September 30, 2016||Download|
Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease.
1 file(s) 2 downloads
|Canavan Disease||October 5, 1993||Download|
Submit Your Research
If you have an article or paper you’d like to submit to the research library, please email Valerie Greger (firstname.lastname@example.org), our Research Director.
If you or a family member is affected by a rare disease and you’d like help reviewing scientific literature, please contact our Family Support Team by emailing Diana Jussila (email@example.com), Director of Family Services, or Becky Benson (firstname.lastname@example.org), Family Services Manager.