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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 imperfecta
A 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 siblings
G 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 imperfecta
A Superti-Furga, P M Royce, F M Pistone, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 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 imperfecta
A 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 siblings
G 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 imperfecta
A Superti-Furga, P M Royce, F M Pistone, et al.
Page
of 1