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Mostrati risultati da 41 a 60 di 275
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
In vivo detection of Choroidal abnormalities related to NF1: Feasibility and comparison with standard NIH diagnostic criteria in pediatric patients 2015 PARROZZANI, RAFFAELECLEMENTI, MAURIZIOFrizziero, LuisaTREVISSON, EVAFUSETTI, STEFANOMIDENA, EDOARDO + INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE - -
FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome. 2015 CASSINA, MATTEOSALVIATI, LEONARDOCLEMENTI, MAURIZIO + AMERICAN JOURNAL OF MEDICAL GENETICS. PART A - American journal of medical genetics. Part A
Neural signatures of the interaction between the 5-HTTLPR genotype and stressful life events in healthy women 2014 FAVARO, ANGELACLEMENTI, MAURIZIOTENCONI, ELENADEGORTES, DANIELAGIANNUNZIO, VALERIASANTONASTASO, PAOLO + PSYCHIATRY RESEARCH. NEUROIMAGING - -
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases. 2014 DEL PRETE, DORELLACLEMENTI, MAURIZIO + CLINICAL GENETICS - -
Using ancestry-informative markers to identify fine structure across 15 populations of European origin 2014 FAVARO, ANGELASANTONASTASO, PAOLOBRUSON, ALICECLEMENTI, MAURIZIODEGORTES, DANIELAFORZAN, MONICATENCONI, ELENA + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Neurofibromatosis type 1 in two siblings due to Maternal Germline Mosaicism. 2014 TREVISSON, EVASALVIATI, LEONARDOCLEMENTI, MAURIZIO + CLINICAL GENETICS - -
First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis. 2014 CASSINA, MATTEOLITTA, PIETRO SALVATORECLEMENTI, MAURIZIO + HUMAN REPRODUCTION UPDATE - -
Pregnancy outcome after methotrexate treatment for rheumatic disease prior to or during early pregnancy: a prospective multicenter cohort study. 2014 CLEMENTI, MAURIZIO + ARTHRITIS & RHEUMATOLOGY - -
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus 2014 ZANETTI, ALESSANDRATOMANIN, ROSELLARAMPAZZO, ANGELICARIGON, CHIARAGASPAROTTO, NICOLETTACASSINA, MATTEOCLEMENTI, MAURIZIOSCARPA, MAURIZIO JIMD REPORTS - -
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas. 2014 TREVISSON, EVAFORZAN, MONICACLEMENTI, MAURIZIO + EUROPEAN JOURNAL OF HUMAN GENETICS - -
High-Resolution Melt as a Screening Method in Autosomal Dominant Polycystic Kidney Disease (ADPKD). 2014 CLEMENTI, MAURIZIORonco C. + JOURNAL OF CLINICAL LABORATORY ANALYSIS - -
A new clinical tool for assessing numerical abilities in neurological diseases: numerical activities of daily living 2014 SEMENZA, CARLOARCARA, GIORGIOBURGIO, FRANCESCABENAVIDES VARELA, SILVIA ELENACLEMENTI, MAURIZIO + FRONTIERS IN AGING NEUROSCIENCE - -
A genome-wide association study of anorexia nervosa 2014 FAVARO, ANGELASANTONASTASO, PAOLOBRUSON, ALICECLEMENTI, MAURIZIODEGORTES, DANIELAFORZAN, MONICATENCONI, ELENA + MOLECULAR PSYCHIATRY - -
Evaluation of tibial osteopathy occurrence in neurofibromatosis Type 1 Italian patients. 2013 CLEMENTI, MAURIZIO + AMERICAN JOURNAL OF MEDICAL GENETICS. PART A - -
Pregnancy outcome in women exposed to antiepileptic drugs: Teratogenic role of maternal epilepsy and its pharmacologic treatment. 2013 CASSINA, MATTEOCLEMENTI, MAURIZIO + REPRODUCTIVE TOXICOLOGY - -
Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families. 2013 CLEMENTI, MAURIZIO + KIDNEY INTERNATIONAL - -
Analysis of p53 polymorphisms in individuals with multiple melanocytic nevi 2013 BRUSON, ALICEZATTRA, EDOARDOCASSINA, MATTEOBALDO, VINCENZOCLEMENTI, MAURIZIOALAIBAC, MAURO SALVATORE ALESSANDRO + EUROPEAN JOURNAL OF DERMATOLOGY - -
Optical Coherence Tomography in the Diagnosis of Optic Pathway Gliomas 2013 PARROZZANI, RAFFAELECLEMENTI, MAURIZIOTREVISSON, EVAG. OrlandoE. PilottoMIDENA, EDOARDO + INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE - -
The outcomes of pregnancy in women exposed to the new macrolides in the first trimester: a prospective, multicentre, observational study. 2012 CLEMENTI, MAURIZIO + DRUG SAFETY - -
The SHOX Gene and The Short Stature. Roundtable On Diagnosis andTreatment of Short Stature Due To SHOX Haploinsufficiency: How Genetics,Radiology And Anthropometry Can Help The Pediatrician in The Diagnostic 2012 CLEMENTI, MAURIZIOFACCHIN, PAOLA + PEDIATRIC ENDOCRINOLOGY REVIEW - -
Mostrati risultati da 41 a 60 di 275
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