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C Borrone

Showing results (21-30 of 89) with videos related to

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Minerva Pediatrica|September 15, 1971
[Description of a case of generalized gangliosidosis]G Biasini, G Della Cella, S Roncari, et al.
Bollettino Dell'Istituto Sieroterapico Milanese|January 1, 1974
Congenital dyskeratosis and immunological defectC Borrone, F Dagna Bricarelli, C Astrice, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
An abnormal amino acid pattern in adenosine deaminase deficiencyC Borrone, M Di Rocco, U Caruso, et al.
Scandinavian Journal of Rheumatology|January 1, 1996
6-methylprednisolone 'mini-pulses': a new modality of glucocorticoid treatment in systemic onset juvenile chronic arthritisP Picco, M Gattorno, A Buoncompagni, et al.
Lancet (London, England)|July 3, 1993
Primary hypothyroidism and 131I-MIBG therapy in neuroblastomaP Picco, A Garaventa, F Claudiani, et al.
Analytical Biochemistry|March 1, 1985
New spectrophotometric assays of acid lipase and their use in the diagnosis of Wolman and cholesteryl ester storage diseasesA Nègre, R Salvayre, A Dagan, et al.
Prenatal Diagnosis|September 1, 1985
Comparative study of 15 lysosomal enzymes in chorionic villi and cultured amniotic fluid cells. Early prenatal diagnosis in seven pregnancies at risk for lysosomal storage diseasesR Gatti, C Lombardo, M Filocamo, et al.
European Journal of Pediatrics|March 1, 1992
Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancyP Picco, L Garibaldi, M Cotellessa, et al.
Helvetica Paediatrica Acta|November 1, 1978
Dextrothyroxine treatment of phosphorylase-kinase deficiency glycogenosis in four boysL R Garibaldi, C Borrone, I de Martini, et al.
Neurology|July 1, 1988
Multisystem triglyceride storage disease is due to a specific defect in the degradation of endocellularly synthesized triglyceridesS Di Donato, B Garavaglia, P Strisciuglio, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Minerva Pediatrica|September 15, 1971
[Description of a case of generalized gangliosidosis]G Biasini, G Della Cella, S Roncari, et al.
Bollettino Dell'Istituto Sieroterapico Milanese|January 1, 1974
Congenital dyskeratosis and immunological defectC Borrone, F Dagna Bricarelli, C Astrice, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
An abnormal amino acid pattern in adenosine deaminase deficiencyC Borrone, M Di Rocco, U Caruso, et al.
Scandinavian Journal of Rheumatology|January 1, 1996
6-methylprednisolone 'mini-pulses': a new modality of glucocorticoid treatment in systemic onset juvenile chronic arthritisP Picco, M Gattorno, A Buoncompagni, et al.
Lancet (London, England)|July 3, 1993
Primary hypothyroidism and 131I-MIBG therapy in neuroblastomaP Picco, A Garaventa, F Claudiani, et al.
Analytical Biochemistry|March 1, 1985
New spectrophotometric assays of acid lipase and their use in the diagnosis of Wolman and cholesteryl ester storage diseasesA Nègre, R Salvayre, A Dagan, et al.
Prenatal Diagnosis|September 1, 1985
Comparative study of 15 lysosomal enzymes in chorionic villi and cultured amniotic fluid cells. Early prenatal diagnosis in seven pregnancies at risk for lysosomal storage diseasesR Gatti, C Lombardo, M Filocamo, et al.
European Journal of Pediatrics|March 1, 1992
Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancyP Picco, L Garibaldi, M Cotellessa, et al.
Helvetica Paediatrica Acta|November 1, 1978
Dextrothyroxine treatment of phosphorylase-kinase deficiency glycogenosis in four boysL R Garibaldi, C Borrone, I de Martini, et al.
Neurology|July 1, 1988
Multisystem triglyceride storage disease is due to a specific defect in the degradation of endocellularly synthesized triglyceridesS Di Donato, B Garavaglia, P Strisciuglio, et al.
Pageof 9