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A Bartuli

Showing results (11-20 of 23) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemiaF Deodato, S Boenzi, C Rizzo, et al.
Pediatric Nephrology (Berlin, Germany)|October 31, 2001
Extracorporeal dialysis in neonatal hyperammonemia: modalities and prognostic indicatorsS Picca, C Dionisi-Vici, D Abeni, et al.
AJNR. American Journal of Neuroradiology|February 1, 1996
Cranial ultrasonography in maple syrup urine diseaseG Fariello, C Dionisi-Vici, C Orazi, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|February 2, 2013
Coinfection in acute gastroenteritis predicts a more severe clinical course in childrenD Valentini, A C Vittucci, A Grandin, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Thricho-rhino-phalangeal syndrome and severe osteoporosis: a rare association or a feature? An effective therapeutic approach with biphosphonatesM Macchiaiolo, M Mennini, M C Digilio, et al.
The Journal of Pediatrics|December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletionM R Mazziotta, E Ricci, E Bertini, et al.
Lymphology|July 27, 2022
A pediatric case of TEK-Related malformations and marfanoid habitus: an incidental finding or a feature?P S Buonuomo, M El Hachem, G Mastrogiorgio, et al.
Lymphology|January 24, 2022
Expanding the spectrum of Gorham Stout disease exploring a single center pediatric case seriesI Rana, P S Buonuomo, G Mastrogiorgio, et al.
Minerva Pediatrica|November 26, 2009
[Multidisciplinary approach]A Bartuli, E Bertini, F Callea, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
Inborn errors of metabolism: an update on epidemiology and on neonatal-onset hyperammonemiaF Deodato, S Boenzi, C Rizzo, et al.
Pediatric Nephrology (Berlin, Germany)|October 31, 2001
Extracorporeal dialysis in neonatal hyperammonemia: modalities and prognostic indicatorsS Picca, C Dionisi-Vici, D Abeni, et al.
AJNR. American Journal of Neuroradiology|February 1, 1996
Cranial ultrasonography in maple syrup urine diseaseG Fariello, C Dionisi-Vici, C Orazi, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|February 2, 2013
Coinfection in acute gastroenteritis predicts a more severe clinical course in childrenD Valentini, A C Vittucci, A Grandin, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
Thricho-rhino-phalangeal syndrome and severe osteoporosis: a rare association or a feature? An effective therapeutic approach with biphosphonatesM Macchiaiolo, M Mennini, M C Digilio, et al.
The Journal of Pediatrics|December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletionM R Mazziotta, E Ricci, E Bertini, et al.
Lymphology|July 27, 2022
A pediatric case of TEK-Related malformations and marfanoid habitus: an incidental finding or a feature?P S Buonuomo, M El Hachem, G Mastrogiorgio, et al.
Lymphology|January 24, 2022
Expanding the spectrum of Gorham Stout disease exploring a single center pediatric case seriesI Rana, P S Buonuomo, G Mastrogiorgio, et al.
Minerva Pediatrica|November 26, 2009
[Multidisciplinary approach]A Bartuli, E Bertini, F Callea, et al.
Pageof 3