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Therapeutic Advances in Musculoskeletal Disease|May 7, 2021
Comparison of three treatment protocols with intra-articular low or intermediate molecular weight hyaluronic acid in early symptomatic knee osteoarthritisFelice Galluccio, Daniela D'Angela, Barbara Polistena, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 16, 2025
Arginase 1 deficiency: a treatable form of spastic paraplegiaAlessandro Burlina, Anna Ardissone, Roberta Battini, et al.
Clinical Rheumatology|December 28, 2011
Longitudinal ultrasound and clinical follow-up of Baker's cysts injection with steroids in knee osteoarthritisFrancesca Bandinelli, Roberto Fedi, Sergio Generini, et al.
Bone|January 2, 2010
Prospective bone ultrasound patterns during childhood acute lymphoblastic leukemia treatmentAlessandro Mussa, Nicoletta Bertorello, Francesco Porta, et al.
Nephrology (Carlton, Vic.)|June 12, 2018
Differential response to renal replacement therapy in neonatal-onset inborn errors of metabolismFrancesco Porta, Licia Peruzzi, Roberto Bonaudo, et al.
BMJ Open Sport & Exercise Medicine|October 13, 2017
The waterpolo shoulder paradigm: results of ultrasound surveillance at poolsideFelice Galluccio, Eleonora Bellucci, Francesco Porta, et al.
Life (Basel, Switzerland)|November 27, 2024
Clinical Efficacy and Safety of Ultrasound-Guided Injection with Low-Molecular-Weight Peptides from Hydrolyzed Collagen in Patients with Partial Supraspinatus Tendon Tears: A Pilot StudyLuca Latini, Francesco Porta, Vincenzo Maccarrone, et al.
Orphanet Journal of Rare Diseases|April 4, 2025
The wide phenotypic spectrum of thiamine metabolism dysfunction syndrome 5 and its treatmentAlice Dallan, Giuseppe Reynolds, Carlotta Canavese, et al.
Italian Journal of Pediatrics|October 26, 2012
Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotypeCristina Lovera, Francesco Porta, Anna Caciotti, et al.
Italian Journal of Pediatrics|October 7, 2024
Triheptanoin in patients with long-chain fatty acid oxidation disorders: clinical experience in ItalyFrancesco Porta, Arianna Maiorana, Vincenza Gragnaniello, et al.
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