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Genetic Testing and Molecular Biomarkers|November 26, 2009
A nationwide genetic testing survey in Italy, year 2007Bruno Dallapiccola, Isabella Torrente, Emanuele Agolini, et al.American Journal of Medical Genetics. Part A|August 12, 2016
Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndromeAgatino Battaglia, Laura Bernardini, Isabella Torrente, et al.European Journal of Human Genetics : EJHG|May 26, 2006
Genetic testing in Italy, year 2004Bruno Dallapiccola, Isabella Torrente, Arnaldo Morena, et al.Asian Journal of Andrology|July 27, 2010
Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocolsRossella Giuliani, Ivana Antonucci, Isabella Torrente, et al.Italian Journal of Pediatrics|February 13, 2013
Four-year follow-up study in a NF1 boy with a focal pontine hamartomaPasquale Parisi, Severino Persechino, Maria Chiara Paolino, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 20, 2013
Spinal neurofibromatosis in a family with classical neurofibromatosis type 1 and a novel NF1 gene mutationFrancesco Nicita, Isabella Torrente, Alberto Spalice, et al.Annals of Human Genetics|August 21, 2009
Founder effects for ATM gene mutations in Italian Ataxia Telangiectasia familiesLuciana Chessa, Maria Piane, Monia Magliozzi, et al.American Journal of Medical Genetics. Part A|May 27, 2010
Germline mosaicism in neurofibromatosis type 1 due to a paternally derived multi-exon deletionIrene Bottillo, Isabella Torrente, Valentina Lanari, et al.American Journal of Medical Genetics. Part A|February 24, 2011
Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1Martino Ruggieri, Mario Mastrangelo, Alberto Spalice, et al.European Journal of Medical Genetics|January 24, 2007
Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlationLaura Bernardini, Anna Capalbo, Maria Gabriella D'Avanzo, et al.Pageof 4