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Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|May 27, 2025
Recovery of functional outcomes after robot assisted radical prostatectomy (RaRP): impact of vacuum therapy compared to PDE5 inhibitors alonePier Paolo Prontera, Francesca Romana Prusciano, Marco Lattarulo, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|October 5, 2020
Predictors of surgical outcomes of retroperitoneal laparoscopic partial nephrectomyCarmine Sciorio, Pier Paolo Prontera, Salvatore Scuzzarella, et al.
American Journal of Medical Genetics. Part A|October 13, 2011
Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndromePaolo Prontera, Emanuela Garelli, Ilenia Isidori, et al.
Genes|June 27, 2024
Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature ReviewMaria Teresa Bonati, Agnese Feresin, Paolo Prontera, et al.
Medicine|July 8, 2020
Intestinal lymphangiectasia in a 3-month-old girl: A case report of Hennekam syndrome caused by CCBE1 mutationAntonella Fattorusso, Elena Sofia Pieri, Giovanni Battista Dell'Isola, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|May 15, 2025
ChatGPT artificial intelligence in clinical data analysis: an example comparing standard vs fusion prostate biopsy outcomes after robotic-assisted radical prostatectomy (RaRP)Pier Paolo Prontera, Francesca Romana Prusciano, Marco Lattarulo, et al.
Public Health Genomics|October 12, 2016
A Clinical and Molecular Survey of 62 Cystic Fibrosis Patients from Umbria (Central Italy) Disclosing a High Frequency (2.4%) of the 2184insA Allele: Implications for ScreeningPaolo Prontera, Ilenia Isidori, Valeria Mencarini, et al.
Biogerontology|January 25, 2015
A genetic-demographic approach reveals a gender-specific association of SLC6A3/DAT1 40 bp-VNTR with life-expectancyFazal Hadi, Serena Dato, Francesco M Carpi, et al.
American Journal of Medical Genetics. Part A|April 6, 2011
Craniometaphyseal dysplasia with severe craniofacial involvement shows homozygosity at 6q21-22.1 locusPaolo Prontera, Daniela Rogaia, Cristina Sobacchi, et al.
American Journal of Medical Genetics. Part A|December 13, 2007
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotypeAlberto Sensi, Paolo Prontera, Barbara Buldrini, et al.
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