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Reports of Practical Oncology and Radiotherapy : Journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology|August 22, 2018
Volumetric image-guided conformal radiotherapy for localized prostate cancer: Analysis of dosimetric and clinical factors affecting acute and late toxicityGianluca Ingrosso, Alessandra Carosi, Daniela di Cristino, et al.
Brain & Development|July 11, 2013
14q12 duplication including FOXG1: is there a common age-dependent epileptic phenotype?Chiara Bertossi, Matteo Cassina, Luca De Palma, et al.
Reports of Practical Oncology and Radiotherapy : Journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology|December 7, 2016
Volumetric image-guided highly conformal radiotherapy of the prostate bed: Toxicity analysisGianluca Ingrosso, Alessandra Carosi, Daniela di Cristino, et al.
Epilepsy Research|November 28, 2017
CNTNAP2 mutations and autosomal dominant epilepsy with auditory featuresEmanuela Leonardi, Emanuela Dazzo, Maria Cristina Aspromonte, et al.
Journal of Human Genetics|December 15, 2015
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disabilitySilvia Moncini, Paola Castronovo, Alessandra Murgia, et al.
Vaccines|November 25, 2020
Vaccination Attitude and Communication in Early Settings: An Exploratory StudyNoemi Mereu, Alessandra Mereu, Alessandra Murgia, et al.
Cells|July 14, 2023
Activation Ratio Correlates with IQ in Female Carriers of the <i>FMR1</i> PremutationDragana Protic, Roberta Polli, Ye Hyun Hwang, et al.
Cancer Investigation|October 28, 2014
Acute and late toxicity after three-dimensional conformal image-guided radiotherapy for localized prostate cancerGianluca Ingrosso, Alessandra Carosi, Elisabetta Ponti, et al.
Annals of Human Genetics|July 6, 2010
Spectrum and frequency of SLC26A4 mutations among Czech patients with early hearing loss with and without Enlarged Vestibular Aqueduct (EVA)Radka Pourová, Petr Janousek, Michal Jurovcík, et al.
Epilepsia|September 29, 2009
Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathyDavide Mei, Carla Marini, Francesca Novara, et al.
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