Jos�, Ben & Life Today
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Great Results Through Understanding
Sat, Mar 18, 2017 -
'Right To Try' Congressional Bill for ALS Patients
Thu, Jul 14, 2016 -
SB Independent - Ice Bucket Challenge: One Year Later
Wed, Aug 19, 2015
The #1 nonprofit biotechnology organization dedicated to developing effective treatments for ALS, the Institute was founded in 1999 and is based in Cambridge, MA.
This is the protocol for the Precision Medicine Program in which Jos� is participating.
The Forbes Norris MDA/ALS Research and Treatment Center carries on the legacy of an internationally renowned physician in the field of Amyotrophic Lateral Sclerosis (ALS) research and clinical care. It is the largest ALS clinical research center in the US
Established in 1985, the Association focuses on research, care services, public education, and public policy � giving help and hope to those facing ALS.
The National ALS Registry is a congressionally mandated registry for persons in the U.S. with ALS. It is the only population-based registry in the U.S. that collects information to help scientists learn more about who gets ALS and its causes.
Information page about ALS from the National Institutes of Health.
La Esclerosis Lateral Amiotr'fica, (ALS, por su sigla en ingl's), es una enfermedad neurol'gica grave que afecta a la capacidad para movernos. Tambi'n se le llama enfermedad de Lou Gehrig. Este sumario le informar' sobre la ALS.