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G Ruffa

Showing results (41-50 of 49) with videos related to

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Minerva Pediatrica|October 30, 1978
[Chronic constrictive pericarditis with protein-losing enteropathy. Diagnosis and surgical treatment in a 9-year-old girl]A Bertolini, R Pongiglione, G L Bava, et al.
Minerva Pediatrica|April 1, 1995
[Osteopetrosis and renal acidosis: a new case of this rare syndrome]G Ruffa, C Milanaccio, P Sbolgi, et al.
Minerva Pediatrica|October 1, 1988
[Research on possible aluminum contamination of commercial milk]L Moni, A Mazzucotelli, A Costa, et al.
Clinical Endocrinology|October 2, 2002
Fasting plasma free fatty acid concentrations and Pro12Ala polymorphism of the peroxisome proliferator-activated receptor (PPAR) gamma2 gene in healthy individualsO Vaccaro, F P Mancini, G Ruffa, et al.
Minerva Pediatrica|February 18, 1975
[Beckwith-Wiedemann syndrome. Presentation of 5 cases]A Delgado, M J Lozano, G Ruffa, et al.
Human Molecular Genetics|April 10, 1999
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivityS Colella, T Nardo, D Mallery, et al.
Minerva Pediatrica|October 31, 1986
[Familial hypercholesterolemia. Study of low-density lipoprotein receptors. Treatment with plasmapheresis]C Bellini, E Bonioli, G Ruffa, et al.
Pediatric Nephrology (Berlin, Germany)|September 7, 2000
Phenotypic variability in Bartter syndrome type IA Bettinelli, S Ciarmatori, L Cesareo, et al.
Human Mutation|October 26, 1999
Jagged-1 mutation analysis in Italian Alagille syndrome patientsG Pilia, M Uda, D Macis, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Minerva Pediatrica|October 30, 1978
[Chronic constrictive pericarditis with protein-losing enteropathy. Diagnosis and surgical treatment in a 9-year-old girl]A Bertolini, R Pongiglione, G L Bava, et al.
Minerva Pediatrica|April 1, 1995
[Osteopetrosis and renal acidosis: a new case of this rare syndrome]G Ruffa, C Milanaccio, P Sbolgi, et al.
Minerva Pediatrica|October 1, 1988
[Research on possible aluminum contamination of commercial milk]L Moni, A Mazzucotelli, A Costa, et al.
Clinical Endocrinology|October 2, 2002
Fasting plasma free fatty acid concentrations and Pro12Ala polymorphism of the peroxisome proliferator-activated receptor (PPAR) gamma2 gene in healthy individualsO Vaccaro, F P Mancini, G Ruffa, et al.
Minerva Pediatrica|February 18, 1975
[Beckwith-Wiedemann syndrome. Presentation of 5 cases]A Delgado, M J Lozano, G Ruffa, et al.
Human Molecular Genetics|April 10, 1999
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivityS Colella, T Nardo, D Mallery, et al.
Minerva Pediatrica|October 31, 1986
[Familial hypercholesterolemia. Study of low-density lipoprotein receptors. Treatment with plasmapheresis]C Bellini, E Bonioli, G Ruffa, et al.
Pediatric Nephrology (Berlin, Germany)|September 7, 2000
Phenotypic variability in Bartter syndrome type IA Bettinelli, S Ciarmatori, L Cesareo, et al.
Human Mutation|October 26, 1999
Jagged-1 mutation analysis in Italian Alagille syndrome patientsG Pilia, M Uda, D Macis, et al.
Pageof 5