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F M Pistone

Showing results (1-10 of 7) with videos related to

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Minerva Pediatrica|March 17, 1970
[Feeding prematures and infants with a new humanized milk]F M Pistone, G Gaiero
Archivio "E. Maragliano" Di Patologia E Clinica|January 1, 1975
[Cytomegalic disease with bronchopneumopathy, autoimmune anemia and malabsorption]F M Pistone, G Gargani, R Cerone
Archivio "E. Maragliano" Di Patologia E Clinica|July 1, 1975
[Anhidrotic ectodermal dysplasia with chronic bronchopneumopathy]F M Pistone, G Gargani, R Cerone
Minerva Pediatrica|March 10, 1975
[Brain damage in mucopolysaccharidosis (33 cases)]M L Grossi-Bianchi, F M Pistone, C Romano
Connective Tissue Research|January 1, 1993
An intronic deletion leading to skipping of exon 21 of COL1A2 in a boy with mild osteogenesis imperfectaA Superti-Furga, M Raghunath, F M Pistone, et al.
Acta Neuropathologica|January 1, 1983
Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblingsG Pellegrini, M Moggio, A Cheldi, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Delayed triple-helix formation of abnormal type I collagen is corrected by reduced temperature. Studies of a family with variable expression of osteogenesis imperfectaA Superti-Furga, P M Royce, F M Pistone, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Minerva Pediatrica|March 17, 1970
[Feeding prematures and infants with a new humanized milk]F M Pistone, G Gaiero
Archivio "E. Maragliano" Di Patologia E Clinica|January 1, 1975
[Cytomegalic disease with bronchopneumopathy, autoimmune anemia and malabsorption]F M Pistone, G Gargani, R Cerone
Archivio "E. Maragliano" Di Patologia E Clinica|July 1, 1975
[Anhidrotic ectodermal dysplasia with chronic bronchopneumopathy]F M Pistone, G Gargani, R Cerone
Minerva Pediatrica|March 10, 1975
[Brain damage in mucopolysaccharidosis (33 cases)]M L Grossi-Bianchi, F M Pistone, C Romano
Connective Tissue Research|January 1, 1993
An intronic deletion leading to skipping of exon 21 of COL1A2 in a boy with mild osteogenesis imperfectaA Superti-Furga, M Raghunath, F M Pistone, et al.
Acta Neuropathologica|January 1, 1983
Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblingsG Pellegrini, M Moggio, A Cheldi, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Delayed triple-helix formation of abnormal type I collagen is corrected by reduced temperature. Studies of a family with variable expression of osteogenesis imperfectaA Superti-Furga, P M Royce, F M Pistone, et al.
Pageof 1