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P Buttitta

Showing results (11-20 of 21) with videos related to

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La Pediatria|January 1, 1970
[On infantile myoclonic encephalopathy with spasms and hypsarrhythmia. Etiopathogenetic and clinico-therapeutic considerations]P Buttitta, M T Carnesi, F Vassallo
La Pediatria|January 1, 1981
[Anhydrotic ectodermal dysplasia. Rare form with vascular purpura and myopathy]P Buttitta, L Giuffre', G Auricchio, et al.
Thrombosis and Haemostasis|October 1, 1996
Haemostatic studies in carbohydrate-deficient glycoprotein syndrome type IA Fiumara, R Barone, P Buttitta, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1985
[A rare cervico-facial teratoma in a newborn female infant]P Buttitta, G Leone, P Sicura, et al.
Journal of Neurology|October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type IL Pavone, A Fiumara, R Barone, et al.
The British Journal of Ophthalmology|November 1, 1994
Carbohydrate deficient glycoprotein syndrome type I: ophthalmic aspects in four Sicilian patientsA Fiumara, R Barone, P Buttitta, et al.
American Journal of Medical Genetics|October 1, 1990
Holoprosencephaly: examples of clinical variability and etiologic heterogeneityG Corsello, P Buttitta, M Cammarata, et al.
Annales De Genetique|January 1, 1991
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detectionE Maserati, F Pasquali, O Zuffardi, et al.
Human Genetics|July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen geneM Mottes, A Sangalli, M Valli, et al.
American Journal of Medical Genetics|December 31, 1997
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE geneG Parenti, P Buttitta, G Meroni, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
La Pediatria|January 1, 1970
[On infantile myoclonic encephalopathy with spasms and hypsarrhythmia. Etiopathogenetic and clinico-therapeutic considerations]P Buttitta, M T Carnesi, F Vassallo
La Pediatria|January 1, 1981
[Anhydrotic ectodermal dysplasia. Rare form with vascular purpura and myopathy]P Buttitta, L Giuffre', G Auricchio, et al.
Thrombosis and Haemostasis|October 1, 1996
Haemostatic studies in carbohydrate-deficient glycoprotein syndrome type IA Fiumara, R Barone, P Buttitta, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1985
[A rare cervico-facial teratoma in a newborn female infant]P Buttitta, G Leone, P Sicura, et al.
Journal of Neurology|October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type IL Pavone, A Fiumara, R Barone, et al.
The British Journal of Ophthalmology|November 1, 1994
Carbohydrate deficient glycoprotein syndrome type I: ophthalmic aspects in four Sicilian patientsA Fiumara, R Barone, P Buttitta, et al.
American Journal of Medical Genetics|October 1, 1990
Holoprosencephaly: examples of clinical variability and etiologic heterogeneityG Corsello, P Buttitta, M Cammarata, et al.
Annales De Genetique|January 1, 1991
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detectionE Maserati, F Pasquali, O Zuffardi, et al.
Human Genetics|July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen geneM Mottes, A Sangalli, M Valli, et al.
American Journal of Medical Genetics|December 31, 1997
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE geneG Parenti, P Buttitta, G Meroni, et al.
Pageof 3