Closed
Kleine-Levin Syndrome Foundation — Medical Research Funding
Medical research funding for Kleine-Levin Syndrome
Last Update: May 13, 2026
Funding available
Varies by project
Timeline
- Receipt of requests is now closed
Location
Canada
Overview
The KLS Foundation funds medical research on Kleine-Levin Syndrome and supports studies aimed at finding a cause and a cure. Research includes genetics, proteomics, actigraphy, and sleep-related studies with patient and healthy volunteer participation.
/100
Opportunity Score
Moderate potential, but conditions must align.
At a glance
Funding available
Financing goals
- Increase social or community impact
- Conduct research and development activities
- Train or support volunteers
Eligible Funding
- Varies by project
Timeline
- Receipt of requests is now closed
Eligible candidates
Eligible Industries
- Health care and social assistance
Location
- Canada
Legal structures
- Non-profit
Annual revenue
- All revenue ranges
Organisation size
- All organization sizes
Audience
- Canadians
Non-profit candidates
Sector of operation
- Research
Target groups
- General public
- Academia / students
Revenue structures
- All structures
Scope
- International
Next Steps
1
Determine your project
2
Validate your eligibility
Activities funded
- Medical research on Kleine-Levin Syndrome.
- Genetics studies related to KLS.
- Proteomics research related to KLS.
- Actigraphy and sleep rhythm studies for KLS.
- Brain scintigraphy and cognition studies related to KLS.
Eligibility
Who is eligible?
- Universities and research institutions.
- Hospitals conducting KLS research.
- Medical researchers and investigators.
Eligible geographic areas
- Stanford University, Palo Alto, California
- Pitié Salpêtrière Hospital, Paris, France
Contacts
Frequently Asked Questions about the Kleine-Levin Syndrome Foundation — Medical Research Funding Program
What is the Kleine-Levin Syndrome Foundation — Medical Research Funding?
The KLS Foundation funds medical research on Kleine-Levin Syndrome and supports studies aimed at finding a cause and a cure. Research includes genetics, proteomics, actigraphy, and sleep-related studies with patient and healthy volunteer participation.
Who is eligible for the Kleine-Levin Syndrome Foundation — Medical Research Funding program?
To be eligible for the Kleine-Levin Syndrome Foundation — Medical Research Funding program, you must:
KLS-focused research only.
Supports cause and cure studies.
May involve volunteer participation.
What expenses are eligible under Kleine-Levin Syndrome Foundation — Medical Research Funding?
Medical research on Kleine-Levin Syndrome.
Genetics studies related to KLS.
Proteomics research related to KLS.
Actigraphy and sleep rhythm studies for KLS.
Brain scintigraphy and cognition studies related to KLS.
Who can I contact for more information about the Kleine-Levin Syndrome Foundation — Medical Research Funding?
You can contact Kleine-Levin Syndrome Foundation (KLSF) by email at maeva.cazeres@aphp.fr or by phone at none.
Where is the Kleine-Levin Syndrome Foundation — Medical Research Funding available?
The Kleine-Levin Syndrome Foundation — Medical Research Funding program is available across Canada.
Is the Kleine-Levin Syndrome Foundation — Medical Research Funding a grant, loan, or tax credit?
Kleine-Levin Syndrome Foundation — Medical Research Funding is a Researchers And Facilities
Who are the financial supporters of the Kleine-Levin Syndrome Foundation — Medical Research Funding?
Kleine-Levin Syndrome Foundation — Medical Research Funding is funded by Kleine-Levin Syndrome Foundation (KLSF)