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C Borrone

Showing results (31-40 of 89) with videos related to

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Minerva Pediatrica|February 15, 1979
[Mannosidosis with severe pulmonary infiltration]P Cerruti Mainardi, S Cavalieri, E Battistini, et al.
Prenatal Diagnosis|March 1, 1985
Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cellsR Gatti, C Borrone, M Filocamo, et al.
American Journal of Medical Genetics|April 15, 1993
New multisystemic disorder involving heart valves, skin, bones, and joints in two brothersC Borrone, M Di Rocco, F Crovato, et al.
Minerva Pediatrica|April 1, 1993
[The Simpson-Golabi-Behmel syndrome. The stages of a diagnostic procedure]M Di Rocco, E Lignana, M Faraci, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1982
[Clinical heterogeneity in fructose intolerance]C Borrone, G Lamedica, M Di Rocco, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Neutropenia and impaired neutrophil function in glycogenosis type IbM Di Rocco, C Borrone, F Dallegri, et al.
Journal of Medical Genetics|March 2, 1999
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndromeM Di Rocco, A Arslanian, M Romanengo, et al.
Minerva Pediatrica|February 4, 1971
[The blastic transformation test in vitro in allergy to cow's milk]C Borrone, F Dagna Bricarelli, L Massimo, et al.
Annals of Neurology|January 1, 1980
Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidationC Angelini, M Philippart, C Borrone, et al.
The Journal of Pediatrics|May 30, 1998
Cutaneous leishmaniasis in a 6-month-old girlM Di rocco, S Vignola, C Borrone, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Minerva Pediatrica|February 15, 1979
[Mannosidosis with severe pulmonary infiltration]P Cerruti Mainardi, S Cavalieri, E Battistini, et al.
Prenatal Diagnosis|March 1, 1985
Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cellsR Gatti, C Borrone, M Filocamo, et al.
American Journal of Medical Genetics|April 15, 1993
New multisystemic disorder involving heart valves, skin, bones, and joints in two brothersC Borrone, M Di Rocco, F Crovato, et al.
Minerva Pediatrica|April 1, 1993
[The Simpson-Golabi-Behmel syndrome. The stages of a diagnostic procedure]M Di Rocco, E Lignana, M Faraci, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1982
[Clinical heterogeneity in fructose intolerance]C Borrone, G Lamedica, M Di Rocco, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Neutropenia and impaired neutrophil function in glycogenosis type IbM Di Rocco, C Borrone, F Dallegri, et al.
Journal of Medical Genetics|March 2, 1999
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndromeM Di Rocco, A Arslanian, M Romanengo, et al.
Minerva Pediatrica|February 4, 1971
[The blastic transformation test in vitro in allergy to cow's milk]C Borrone, F Dagna Bricarelli, L Massimo, et al.
Annals of Neurology|January 1, 1980
Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidationC Angelini, M Philippart, C Borrone, et al.
The Journal of Pediatrics|May 30, 1998
Cutaneous leishmaniasis in a 6-month-old girlM Di rocco, S Vignola, C Borrone, et al.
Pageof 9