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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
Here are answers to the most common questions about the Kleine-Levin Syndrome Foundation — Medical Research Funding. This section explains what the program is, how much funding is available, eligibility requirements, application deadlines, and other important details to help you determine if this grant is right for your business.
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)