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Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|August 2, 2012
The effect of clodronate on a mevalonate kinase deficiency cellular modelValentina Zanin, Annalisa Marcuzzi, Elisa Piscianz, et al.Micromachines|May 27, 2026
A Droplet-Based Microfluidic Platform for Rapid Optical Detection of Bacteria: Proof-of-Concept for Radiopharmaceutical Sterility TestingAdriano Colombelli, Daniela Lospinoso, Vita Guarino, et al.Gene|December 18, 2017
Genetic profile of patients with early onset inflammatory bowel diseaseMartina Girardelli, Federica Basaldella, Sara Della Paolera, et al.Journal of Pediatric Gastroenterology and Nutrition|February 7, 2022
MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase PhenotypeLorenza Matarazzo, Anna Monica Bianco, Emmanouil Athanasakis, et al.Journal of Pediatric Hematology/Oncology|November 28, 2017
The Challenge of Next Generation Sequencing in a Boy With Severe Mononucleosis and EBV-related LymphomaFederico Verzegnassi, Erica Valencic, Valentina Kiren, et al.Medical Hypotheses|February 8, 2012
A common genetic background could explain early-onset Crohn's diseaseAnna Monica Bianco, Valentina Zanin, Martina Girardelli, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 5, 2012
Lovastatin-induced apoptosis is modulated by geranylgeraniol in a neuroblastoma cell lineAnnalisa Marcuzzi, Valentina Zanin, Elisa Piscianz, et al.Langmuir : the ACS Journal of Surfaces and Colloids|April 19, 2023
Sunset Yellow Confined in Curved Geometry: A Microfluidic ApproachCaterina Maria Tone, Alessandra Zizzari, Lorenza Spina, et al.Nanomaterials (Basel, Switzerland)|November 24, 2023
Polymeric Membranes Doped with Halloysite Nanotubes Imaged using Proton Microbeam MicroscopyGiovanna Vasco, Valentina Arima, Soufiane Boudjelida, et al.European Journal of Medical Genetics|July 7, 2010
A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defectSilvia Vettore, Daniela De Rocco, Bernhard Gerber, et al.Pageof 5