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Daniela Concolino

Showing results (1-10 of 80) with videos related to

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Metabolites|November 7, 2014
New Strategies for the Treatment of Phenylketonuria (PKU)Pietro Strisciuglio, Daniela Concolino
European Journal of Internal Medicine|August 16, 2014
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry diseaseDaniela Concolino, Emilia Degennaro, Rossella Parini, et al.
Journal of Clinical Medicine|August 12, 2023
Left Atrial Strain in Cardiomyopathies and Congenital Heart Disease: A Call for Its Integration into Clinical PracticeGiulia Pelaia, Daniela Concolino, Jolanda Sabatino
Current Pharmaceutical Design|March 2, 2013
Anderson-Fabry disease in childrenSimona Sestito, Ferdinando Ceravolo, Daniela Concolino
Italian Journal of Pediatrics|November 17, 2018
Enzyme replacement therapy: efficacy and limitationsDaniela Concolino, Federica Deodato, Rossella Parini
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 2005
Early detection of podiatric anomalies in children with Down syndromeDaniela Concolino, Antonietta Pasquzzi, Giuseppe Capalbo, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 23, 2014
Successful management of neonatal renal venous thrombosisAntonio Piscitelli, Rossella Galiano, Vincenzo Piccolo, et al.
Molecular Genetics and Metabolism|February 14, 2012
Dopamine agonists in dihydropteridine reductase deficiencyFrancesco Porta, Alessandro Mussa, Daniela Concolino, et al.
European Journal of Pediatrics|August 31, 2013
Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathyFerdinando Ceravolo, Sonia Messina, Carmelo Rodolico, et al.
Human Mutation|February 22, 2002
Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathyGiovanni Cuda, Andrea Mussari, Daniela Concolino, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Metabolites|November 7, 2014
New Strategies for the Treatment of Phenylketonuria (PKU)Pietro Strisciuglio, Daniela Concolino
European Journal of Internal Medicine|August 16, 2014
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry diseaseDaniela Concolino, Emilia Degennaro, Rossella Parini, et al.
Journal of Clinical Medicine|August 12, 2023
Left Atrial Strain in Cardiomyopathies and Congenital Heart Disease: A Call for Its Integration into Clinical PracticeGiulia Pelaia, Daniela Concolino, Jolanda Sabatino
Current Pharmaceutical Design|March 2, 2013
Anderson-Fabry disease in childrenSimona Sestito, Ferdinando Ceravolo, Daniela Concolino
Italian Journal of Pediatrics|November 17, 2018
Enzyme replacement therapy: efficacy and limitationsDaniela Concolino, Federica Deodato, Rossella Parini
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 2005
Early detection of podiatric anomalies in children with Down syndromeDaniela Concolino, Antonietta Pasquzzi, Giuseppe Capalbo, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 23, 2014
Successful management of neonatal renal venous thrombosisAntonio Piscitelli, Rossella Galiano, Vincenzo Piccolo, et al.
Molecular Genetics and Metabolism|February 14, 2012
Dopamine agonists in dihydropteridine reductase deficiencyFrancesco Porta, Alessandro Mussa, Daniela Concolino, et al.
European Journal of Pediatrics|August 31, 2013
Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathyFerdinando Ceravolo, Sonia Messina, Carmelo Rodolico, et al.
Human Mutation|February 22, 2002
Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathyGiovanni Cuda, Andrea Mussari, Daniela Concolino, et al.
Pageof 8