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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta-Analysis of Previously Published Studies 2017 Collantoni, EnricoSolmi, MarcoGallicchio, DavideSantonastaso, PaoloMENEGUZZO, PAOLOClementi, MaurizioPINATO, CLAUDIAForzan, MonicaCassina, MatteoSiani, RobertaTenconi, ElenaVeronese, NicolaFavaro, Angela + EUROPEAN EATING DISORDERS REVIEW - -
Congenital anomalies in contaminated sites: A multisite study in Italy 2017 CASSINA, MATTEOCLEMENTI, MAURIZIO + INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH - -
Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1 2017 TREVISSON, EVACASSINA, MATTEOOPOCHER, ENRICOVICENZI, VIRGINIALUCCHETTA, MARTAPARROZZANI, RAFFAELEMIGLIONICO, GIACOMOMARDARI, RODICAVISCARDI, ELISABETTAMIDENA, EDOARDOCLEMENTI, MAURIZIO JOURNAL OF NEURO-ONCOLOGY - -
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling 2017 Favaro, AngelaSantonastaso, PaoloMonteleone, PalmieroBruson, AliceClementi, MaurizioDegortes, DanielaForzan, MonicaTenconi, ElenaGambaro, Giovanni + SCIENTIFIC REPORTS - -
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa 2017 CASSINA, MATTEOCLEMENTI, MAURIZIODEGORTES, DANIELAFAVARO, ANGELAFORZAN, MONICASANTONASTASO, PAOLOTENCONI, ELENA + THE AMERICAN JOURNAL OF PSYCHIATRY - -
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index 2017 FAVARO, ANGELASANTONASTASO, PAOLOBRUSON, ALICECLEMENTI, MAURIZIODEGORTES, DANIELAFORZAN, MONICATENCONI, ELENA + MOLECULAR PSYCHIATRY - -
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 2016 CASSINA, MATTEOCLEMENTI, MAURIZIO + CLINICAL EPIGENETICS - -
Clinical and genetic correlates of decision making in anorexia nervosa 2016 TENCONI, ELENADEGORTES, DANIELACLEMENTI, MAURIZIOCOLLANTONI, ENRICOCASSINA, MATTEOSANTONASTASO, PAOLOFAVARO, ANGELA + NEUROPSYCHOLOGY, DEVELOPMENT, AND COGNITION. SECTION A, JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY - -
Functional connectivity correlates of response inhibition impairment in anorexia nervosa 2016 COLLANTONI, ENRICOTENCONI, ELENADEGORTES, DANIELAManara, RenzoCLEMENTI, MAURIZIOCASSINA, MATTEOSANTONASTASO, PAOLOFAVARO, ANGELA + PSYCHIATRY RESEARCH. NEUROIMAGING - -
Advising Mothers on the Use of Medications during Breastfeeding : A Need for a Positive Attitude 2016 CLEMENTI, MAURIZIO + JOURNAL OF HUMAN LACTATION - -
Regression of gadolinium-enhanced lesions in patients affected by neurofibromatosis type 1 2016 LUCCHETTA, MARTAManara, RenzoPERILONGO, GIORGIOCLEMENTI, MAURIZIOTREVISSON, EVA LA RADIOLOGIA MEDICA - -
Serotonin transporter gene polymorphism in eating disorders: Data from a new biobank and META-analysis of previous studies 2016 SOLMI, MARCOGALLICCHIO, DAVIDECOLLANTONI, ENRICOCLEMENTI, MAURIZIOCASSINA, MATTEOFONTANA, FABIOLAGIANNUNZIO, VALERIASiani, RobertaSANTONASTASO, PAOLOTENCONI, ELENAVERONESE, NICOLAFAVARO, ANGELA + THE WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY - -
Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns 2016 CASSINA, MATTEORUOL, MICHELEPERTILE, RICCARDOMIDRIO, PAOLAVICENZI, VIRGINIAGAMBA, PIERGIORGIOCLEMENTI, MAURIZIO + BIRTH DEFECTS RESEARCH. PART A, CLINICAL AND MOLECULAR TERATOLOGY - -
Pregnancy outcome following maternal exposure to mirtazapine: a multicenter, prospective study. 2015 CLEMENTI, MAURIZIO + JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY - -
Ichthyosis and Kallmann syndrome: Not always a contiguous gene syndrome 2015 TREVISSON, EVALUDWIG, KATHRINRenzo ManaraCLEMENTI, MAURIZIOSALVIATI, LEONARDO + JOURNAL OF DERMATOLOGICAL SCIENCE - -
Validation of CFTR intronic variants identified during cystic fibrosis population screening by a minigene splicing assay. 2015 CASARIN, ALBERTOTREVISSON, EVACASSINA, MATTEOCLEMENTI, MAURIZIOSALVIATI, LEONARDO + CLINICAL CHEMISTRY AND LABORATORY MEDICINE - -
The role of cell-free plasma DNA in peritoneal dialysis patients with peritonitis 2015 BROCCA, ALESSANDRACLEMENTI, MAURIZIORonco, Claudio + PERITONEAL DIALYSIS INTERNATIONAL - -
Is there a link between COQ6 and schwannomatosis? 2015 TREVISSON, EVACLEMENTI, MAURIZIOSALVIATI, LEONARDO GENETICS IN MEDICINE - -
Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure. 2015 Desbats MALUNARDI, GIADACASARIN, ALBERTODOIMO, MARASPINAZZI, MARCOANGELINI, CORRADOBURLINA, ALBERTOCHIANDETTI, LINOCLEMENTI, MAURIZIOTREVISSON, EVASALVIATI, LEONARDO + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Advances in the pathogenesis of cardiorenal syndrome type 3 2015 BROCCA, ALESSANDRACLEMENTI, MAURIZIORonco, Claudio + OXIDATIVE MEDICINE AND CELLULAR LONGEVITY - -
Mostrati risultati da 21 a 40 di 275
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