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Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Chiropractic care for hypertension: Review of the literature and study of biological and genetic basesStephanie Gb Sullivan, Stefano Paolacci, Aysha Karim Kiani, et al.
Lymphatic Research and Biology|November 16, 2019
Electrical Stimulation in the Treatment of Lymphedema and Associated Skin UlcersMirko Baglivo, Francesco Martelli, Stefano Paolacci, et al.
Journal of Preventive Medicine and Hygiene|December 8, 2022
Ion mobility mass spectrometry with surface activated chemical ionisation as a method for studying the domain of water clustersSimone Cristoni, Martina Larini, Simone Madama, et al.
Acta Bio-Medica : Atenei Parmensis|November 10, 2020
Genetic and physiological autonomic nervous system factors involved in failed back surgery syndrome: A review of the literature and report of nine cases treated with pulsed radiofrequencyManuela Baronio, Mirko Baglivo, Giuseppe Natalini, et al.
Journal of Biotechnology|December 4, 2019
Molecular pathways involved in lymphedema: Hydroxytyrosol as a candidate natural compound for treating the effects of lymph accumulationMatteo Bertelli, Aysha Karim Kiani, Stefano Paolacci, et al.
Journal of Medical Genetics|February 15, 2018
Genetic tests in lymphatic vascular malformations and lymphedemaSandro Michelini, Stefano Paolacci, Elena Manara, et al.
American Journal of Medical Genetics. Part A|April 28, 2017
Wiedemann-Rautenstrauch syndrome: A phenotype analysisStefano Paolacci, Debora Bertola, José Franco, et al.
Acta Bio-Medica : Atenei Parmensis|October 3, 2019
Diagnostic and therapeutic implements based on advanced Biotechnology should be available in low-income countriesMatteo Bertelli, Stefano Paolacci, Tommaso Beccari, et al.
Journal of Clinical Medicine|September 30, 2020
Paraneoplastic Neurological Syndromes: Study of Prevalence in a Province of the Lombardy Region, ItalyLorenzo Lorusso, Vincenza Precone, Daniela Ferrari, et al.
European Journal of Human Genetics : EJHG|June 20, 2020
Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndromeSehime Gulsun Temel, Mahmut Cerkez Ergoren, Elena Manara, et al.
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