Enza Maria Valente vince il bando Fondazione Cariplo e Fondazione Telethon - Fondazione Mondino
c:p. n°111.. - Prot. n°41..361.del OltJoLl2.D2.0
Solving mendelian mysteries: the non-coding genome may hold the key
IJMS | Free Full-Text | Genome-Wide DNA Methylation Analysis of a Cohort of 41 Patients Affected by Oculo-Auriculo-Vertebral Spectrum (OAVS)
La ricerca italiana in Europa: una sfida da vincere / Enza Maria Valente - YouTube
Rome, January 12th 2006
Loop | Enza Maria Valente
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Monogenic Portal Development Working Group - GP2
Enza Maria Valente vince il bando Fondazione Cariplo e Fondazione Telethon - Fondazione Mondino
Enza Valente - Administrative Coordinator - Bristol-Myers Squibb | LinkedIn
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GBA‐Related Parkinson's Disease: Dissection of Genotype–Phenotype Correlates in a Large Italian Cohort
WITHDRAWN: Schuurs-Hoeijmakers syndrome: Severe expression of the recurrent PACS1 c.607C>T mutation
Genetica Epigenetica Telomeri Longevità. Enza M. Valente. Pink 1, Parkinson da gene mutato - YouTube
Lab Valente | Dipartimento di Medicina Molecolare
Benign Hereditary Chorea as a Manifestation of HPCA Mutation - Brunetti - Movement Disorders Clinical Practice - Wiley Online Library
I “Martedì della Clinica Neurologica” con Enza Maria Valente "Non è detto che sia Parkinson" il 13 marzo 2018 Eventi a Padova
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Neurodevelopmental ciliopathies: a multimodel approach from molecular mechanisms to patients variant interpretation and treatmen
Introduction to human and medical genetics
Enza Maria VALENTE | University of Pavia, Pavia | UNIPV | Department of Molecular Medicine | Research profile
