Associazione Luigi Comini is a specialized philanthropic funder focused on curing and studying mitochondrial and pediatric diseases, with a clear emphasis on rare, medically serious conditions such as Pearson syndrome, KSS, and mtDNA deletion disorders. It supports scientific research teams through direct competitive project grants, suggesting a preference for high-quality biomedical research with translational potential and strong institutional leadership. The presence of prominent scientific committee members from pediatric hospitals and research institutes indicates that it funds credible, research-driven projects rather than broad charitable programs.
Competitive direct research grants and project funding, with grant sizes ranging roughly from $20,000 to $377,955. Likely awards are tied to specific scientific proposals and institutional research teams, with an international reach across Italy, Europe, and beyond.
Applicants should propose well-defined mitochondrial or pediatric rare disease research projects with strong scientific merit and clear translational value. Priority is likely given to established research teams and institutions aligned with the foundation’s medical advisory network; check the foundation website for any calls, eligibility rules, and submission windows, as funding appears to be competitive and project-based.
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Financiamiento actual y próximo de Associazione Luigi Comini - Ente Filantropico al que tu organización sin fines de lucro podría postularse.
¿Quién puede postularse? Progetti di ricerca scientifica e di studio su malattie mitocondriali; il sito indica che i fondi vengono erogati ad enti senza scopo di lucro. Non sono indicati criteri formali di eleggibilità pubblici.
¿Quién puede postularse? Research projects related to mitochondrial diseases; applicants are research groups based in universities, hospitals or non-profit research institutions. The association's Scientific Committee evaluates and selects projects.
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