Buyers Health Care Action Group

A coalition focused on #healthcare, uniting employers around common issues, and improving patient experiences and outcomes for Minnesotans.

• Specifically Named Diseases Research

• 983.

Selective Mutism Research Institute

The SMart Center is a comprehensive Selective Mutism treatment center directed by Dr.

• Religious Related, Spiritual Development N.E.C.

• 984.

Ancient Free & Accepted Masons of Oklahoma

To develop and implement programs to assist the lodges in becoming more visible and active in the communities and to promote Friendship, Morality and Brotherly Love throughout the state.

• Research Institutes and/or Public Policy Analysis

• 985.

Neurodegeneration Therapeutics Inc

CONDUCT BIOMEDICAL RESEARCH Neurodegeneration Therapeutics Inc NTI is 501c3 notforprofit biomedical research company that exists both to discover knowledge about the heterogeneity of adult brain diseases Alzheimers AD Parkinsons PD Lou Gherigs aka ALS and to develop novel personalized therapies for these disorders.

• Single Organization Support

• 986.

Meritcare Health Enterprises Incorporated

The mission of Sanford "Dedicated to the Work of Health and Healing" and the vision "Improving the Human Condition Through Exceptional Care, Innovation and Discovery" is the constant force that drive the organization's plans, decisions and actions.

NATIONAL MENINGITIS ASSOCIATION INC

NMA was established in 2002 by parents whose children either died from or were severely affected by meningococcal disease.

• Nerve, Muscle, and Bone Research

• 988.

Rampy MS Research Foundation

Join us in bringing encouragement to the world of MS through research, endurance sports & community.

• Brain Disorders

• 989.

Subramaniam Foundation for Global Brain Health

Founder & CEO: Dr. Thirusivapragasam Subramaniam (Siva) Create innovative technologies that will eradicate the disability of Hydrocephalus in children.

• Birth Defects, Genetic Diseases

• 990.

CTNNB1 SYNDROME AWARENESS WORLDWIDE

CTNNB1 Syndrome refers to complications resulting from either a mutation or deletion of the CTNNB1 gene.