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Elisabetta Salvatici

Showing results (1-10 of 24) with videos related to

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Clinical Case Reports|February 14, 2022
PMM2-CDG and nephrotic syndrome: A case reportGiuseppe Banderali, Elisabetta Salvatici, Valentina Rovelli, et al.
Nutrition & Metabolism|February 7, 2012
Phenylketonuria: nutritional advances and challengesMarcello Giovannini, Elvira Verduci, Elisabetta Salvatici, et al.
Journal of the American College of Nutrition|April 15, 2014
Randomized controlled trial of a protein substitute with prolonged release on the protein status of children with phenylketonuriaMarcello Giovannini, Enrica Riva, Elisabetta Salvatici, et al.
Minerva Pediatrica|May 6, 2017
Psychological and psychosocial implications for parenting a child with phenylketonuria: a systematic reviewLidia Borghi, Elisabetta Salvatici, Enrica Riva, et al.
Minerva Pediatrics|April 14, 2018
Psychological wellbeing in parents of children with phenylketonuria and association with treatment adherenceLidia Borghi, Elisabetta Salvatici, Giuseppe Banderali, et al.
Journal of Medical Case Reports|April 18, 2012
Fabry disease presenting with sudden hearing loss and otosclerosis: a case reportGiovanni Felisati, Elisabetta Salvatici, Carlotta Pipolo, et al.
Molecular Genetics and Metabolism|November 25, 2020
Retrospective analysis of 19 patients with 6-Pyruvoyl Tetrahydropterin Synthase Deficiency: Prolactin levels inversely correlate with growthFrancesca Manzoni, Elisabetta Salvatici, Alberto Burlina, et al.
The Journal of Nutrition|May 27, 2011
A specific prebiotic mixture added to starting infant formula has long-lasting bifidogenic effectsFilippo Salvini, Enrica Riva, Elisabetta Salvatici, et al.
American Journal of Medical Genetics. Part A|March 22, 2020
PIGW-related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literatureAngela Peron, Maria Iascone, Elisabetta Salvatici, et al.
Molecular Genetics and Metabolism Reports|August 21, 2023
Low bone mineralization in phenylketonuria may be due to undiagnosed metabolic acidosisValentina Rovelli, Vittoria Ercoli, Alice Re Dionigi, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Clinical Case Reports|February 14, 2022
PMM2-CDG and nephrotic syndrome: A case reportGiuseppe Banderali, Elisabetta Salvatici, Valentina Rovelli, et al.
Nutrition & Metabolism|February 7, 2012
Phenylketonuria: nutritional advances and challengesMarcello Giovannini, Elvira Verduci, Elisabetta Salvatici, et al.
Journal of the American College of Nutrition|April 15, 2014
Randomized controlled trial of a protein substitute with prolonged release on the protein status of children with phenylketonuriaMarcello Giovannini, Enrica Riva, Elisabetta Salvatici, et al.
Minerva Pediatrica|May 6, 2017
Psychological and psychosocial implications for parenting a child with phenylketonuria: a systematic reviewLidia Borghi, Elisabetta Salvatici, Enrica Riva, et al.
Minerva Pediatrics|April 14, 2018
Psychological wellbeing in parents of children with phenylketonuria and association with treatment adherenceLidia Borghi, Elisabetta Salvatici, Giuseppe Banderali, et al.
Journal of Medical Case Reports|April 18, 2012
Fabry disease presenting with sudden hearing loss and otosclerosis: a case reportGiovanni Felisati, Elisabetta Salvatici, Carlotta Pipolo, et al.
Molecular Genetics and Metabolism|November 25, 2020
Retrospective analysis of 19 patients with 6-Pyruvoyl Tetrahydropterin Synthase Deficiency: Prolactin levels inversely correlate with growthFrancesca Manzoni, Elisabetta Salvatici, Alberto Burlina, et al.
The Journal of Nutrition|May 27, 2011
A specific prebiotic mixture added to starting infant formula has long-lasting bifidogenic effectsFilippo Salvini, Enrica Riva, Elisabetta Salvatici, et al.
American Journal of Medical Genetics. Part A|March 22, 2020
PIGW-related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literatureAngela Peron, Maria Iascone, Elisabetta Salvatici, et al.
Molecular Genetics and Metabolism Reports|August 21, 2023
Low bone mineralization in phenylketonuria may be due to undiagnosed metabolic acidosisValentina Rovelli, Vittoria Ercoli, Alice Re Dionigi, et al.
Pageof 3