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July 2016
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By Mathew Forbes Romer Foundation
Sold Out Crowd of 200, Including Friends, Family & South Florida Leaders, Came Together to Raise Awareness and Funds for Children's Genetic Diseases of the Brain
By The Mathew Forbes Romer Foundation
See the Light Award Winners Include Mr. Ron Assaf and Dr. Gustavo Maegaway for their Commitment to Advancing the Foundation's Mission and Research Goals
By The Mathew Forbes Romer Foundation
South Florida Genetic Screening and Education Fair, New At-Home Screening Option, Gala and Awards Banquet, and Movie Screening will Take Place February 22, 2015
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By Matthew Forbes Romer Foundation
Foundation is Focused on Education & Research of Children’s Genetic Diseases of the Brain; Event will Celebrate Honorees, Entertain Attendees with ‘The Capitol Steps’ Comedy Show, and Update Guests on This Year’s New and Exciting Progra
By NTSAD
First human trial for Tay-Sachs, Canavan and other rare enzyme deficiency diseases plans to begin in early 2013 thanks to NTSAD, the nation's oldest patient advocacy organization, which leads efforts to find a cure or treatment.
By National Tay-Sachs & Allied Diseases Association
NTSAD Family Conference will bring together 300-plus people from around the world; To focus on research findings, family support and practical tips
By National Tay-Sachs & Allied Diseases Association
Leading the Fight to Treat and Cure Tay-Sachs, Canavan and Related Fatal Genetic Diseases in Children, NTSAD Provides Families with Group and Individual Support, Research Updates and Education During Four-Day Event
By Mathew Forbes Romer Foundation
Emotional Event Celebrates Boca Raton Rabbi and Massachusetts Doctor for Their Work; Honors Numerous Children and Their Families Afflicted with Fatal Genetic Diseases
By www.twitter.com/taysachs
An International Health Care Campaign To Help Fight Disease Was Launched On Twitter at www.twitter.com/taysachs.

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