Որոնման արդյունքները - Roberto Giorda
- Ցուցադրվում են 1 - 20 արդյունքները 34
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KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia Sara Mascheretti, Valentina Riva, Roberto Giorda, Silvana Beri, Lara Francesca Emilia Lanzoni, Maria Rosaria Cellino, Cecilia Marino
Հրապարակվել է 2014Artigo -
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Analysis of the Structure and Expression of the Augmenter of Liver Regeneration (ALR) Gene Roberto Giorda, Michio Hagiya, Tatsuya Seki, Manabu Shimonishi, Harumi Sakai, James Michaelson, A. Francavilla, Thomas E. Starzl, Massimo Trucco
Հրապարակվել է 1996Artigo -
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Association of short‐term memory with a variant within<i> DYX1C1 </i>in developmental dyslexia Cecilia Marino, Andrea Citterio, Roberto Giorda, Andrea Facoetti, Giorgia Menozzi, Laura Vanzin, Maria Luisa Lorusso, Maria Nobile, Massimo Molteni
Հրապարակվել է 2006Artigo -
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Pain-related stress during the Neonatal Intensive Care Unit stay and SLC6A4 methylation in very preterm infants Livio Provenzi, Monica Fumagalli, Ida Sirgiovanni, Roberto Giorda, Uberto Pozzoli, Francesco Morandi, Silvana Beri, Giorgia Menozzi, Fabio Mosca, Renato Borgatti, Rosario Montirosso
Հրապարակվել է 2015Artigo -
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An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypes Sara Mascheretti, Alexandre Bureau, Marco Battaglia, D. Simone, Ermanno Quadrelli, Jordie Croteau, Maria Rosaria Cellino, Roberto Giorda, Silvana Beri, Michel Maziade, Cecilia Marino
Հրապարակվել է 2012Artigo -
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A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia Cecilia Marino, Roberto Giorda, Maria Luisa Lorusso, Laura Vanzin, Nello Salandi, Maria Nobile, Alessandra Citterio, Silvana Beri, Valentina Crespi, Marco Battaglia, Massimo Molteni
Հրապարակվել է 2005Artigo -
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Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation Renata Bocciardi, Roberto Giorda, Jens Buttgereit, Stefania Gimelli, Maria Teresa Divizia, Silvana Beri, Silvio Garofalo, Sara Tavella, Margherita Lerone, Orsetta Zuffardi, Michael Bäder, Roberto Ravazzolo, Giorgio Gimelli
Հրապարակվել է 2007Artigo -
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The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia Cecilia Marino, Paola Scifo, Pasquale Anthony Della Rosa, Sara Mascheretti, Andrea Facoetti, Maria Luisa Lorusso, Roberto Giorda, Monica Consonni, Andrea Falini, Massimo Molteni, Jeffrey R. Gruen, Daniela Perani
Հրապարակվել է 2014Artigo -
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Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements Sabrina Giglio, Karl W. Broman, Naomichi Matsumoto, Vladimiro Calvari, Giorgio Gimelli, Thomas Neumann, Hirofumi Ohashi, Lucille Voullaire, Daniela Larizza, Roberto Giorda, Jim L. Weber, David H. Ledbetter, Orsetta Zuffardi
Հրապարակվել է 2001Artigo -
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From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth Monica Fumagalli, Livio Provenzi, Pietro De Carli, Francesca Dessimone, Ida Sirgiovanni, Roberto Giorda, Claudia Cinnante, Letizia Squarcina, Uberto Pozzoli, Fabio Triulzi, Paolo Brambilla, Renato Borgatti, Fabio Mosca, Rosario Montirosso
Հրապարակվել է 2018Artigo -
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A novel<i>CLN8</i>mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function Chiara Vantaggiato, Francesca Redaelli, Sestina Falcone, Cristiana Perrotta, Alessandra Tonelli, Sara Bondioni, Michela Morbin, Daria Riva, Veronica Saletti, María Clara Bonaglia, Roberto Giorda, Nereo Bresolin, Emilio Clementi, Maria Teresa Bassi
Հրապարակվել է 2009Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Gene
Medicine
Psychology
Chromosome
Phenotype
Mutation
Breakpoint
Dyslexia
Law
Political science
Reading (process)
Chromosomal translocation
Endocrinology
Genotype
Karyotype
Allele
Biochemistry
Computer science
Developmental psychology
Disease
Gene duplication
Genome
Internal medicine
Molecular biology
Neuroscience
Pathology
Proband
Psychiatry