• Epilepsy

• 91.

Epilepsy Foundation of Southeast Tennessee

We are a non-profit agency providing educational, vocational, and outreach services to people with epilepsy, their families and their communities.

• Fund Raising and/or Fund Distribution

• 92.

Eleanor Kaplan Foundation Inc

To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.

Malan Syndrome Foundation Inc

Malan syndrome is a rare genetic disorder that is the result of a change in the NFIX gene.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

• Patient Services�Entertainment, Recreation

• 95.

Idefine Inc

IDefine is committed to identifying life-changing treatments & cures and building community for those with Kleefstra Syndrome and intellectual disabilities.

MICKIE'S MIRACLES INC

Learn the History Behind Mickies Miracles Mickies Miracles advocated for parents to get their child an urgent diagnosis and the highest level of care at Level IV Pediatric Epilepsy Centers increased awareness about the catastrophic dangers of pediatric epilepsy and fought for legislative change to reduce barriers to care and research funding.

• Science & Technology Research Institutes, Services N.E.C.

• 97.

HUDSON-ALPHA INSTITUTE FOR

A nonprofit institute where scientists, educators, clinicians and entrepreneurs collaborate and apply genomics to improve the human condition around the globe.

• Science, General (includes Interdisciplinary Scientific Activities)

• 98.

SPARK NS INC

Advancing Academic Discoveries in Neuroscience.

International Rett Syndrome Foundation

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.