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U-M researchers reveal how a mutated protein acts as risk factor in Parkinson’s disease

In about a fifth of the cases of Parkinson’s disease, [...]

By Michael Foley|2022-07-27T15:52:34+00:00June 23, 2022|Uncategorized|Comments Off

Using genetic screening for selecting the ‘best’ embryo in IVF

Each year, tens of thousands of babies are born in [...]

By Michael Foley|2022-07-27T15:54:26+00:00October 12, 2021|Uncategorized|Comments Off

A new combination therapy for treating rare, fatal Sanfilippo syndrome in children

A study aiming to develop a new therapeutic technique could [...]

By Michael Foley|2022-07-27T15:57:09+00:00February 24, 2021|Uncategorized|Comments Off

National Tay-Sachs & Allied Diseases Association (NTSAD) leads the worldwide fight to treat and cure Tay-Sachs, Canavan, GM1, and Sandhoff diseases by driving research, forging collaboration, and fostering community. Supporting families is the center of everything we do.

The content of this website is intended for informational purposes only and not intended to be a substitute for professional medical advice, diagnosis, or treatment.

The National Tay-Sachs & Allied Diseases Association (NTSAD) leads the worldwide fight to treat and cure Tay-Sachs, Canavan, GM1, and Sandhoff diseases by driving research, forging collaboration, and fostering community. Supporting families is the center of everything we do.

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Get the latest news from NTSAD about our Community, the research that provides hope, and what is happening in the world of rare disease.

2001 Beacon Street, Suite 204
Boston, MA 02135
(617) 277-4463
info@ntsad.org

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National Tay-Sachs & Allied Diseases Association
2001 Beacon Street, Suite 204, Boston, MA 02135
(617) 277-4463 | info@ntsad.org