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L Pavone

Showing results (81-90 of 165) with videos related to

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American Journal of Diseases of Children (1960)|July 1, 1980
Picture of the month. Metaphyseal chondrodysplasia, Schmid typeS S Gellis, M Feingold, L Pavone, et al.
Clinical Pediatrics|April 1, 1996
Multiple sclerosis with onset at 35 months of ageM Ruggieri, A Fiumara, L M Grimaldi, et al.
American Journal of Medical Genetics|October 1, 1993
Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicismR Rizzo, L Pavone, G Micali, et al.
Acta Neurologica|August 1, 1984
Peculiar congenital myopathy in two siblings. Congenital fibre type disproportion or type II fibres hypotrophy?L Pavone, R Scelsi, F Gullotta, et al.
Journal of Child Neurology|August 2, 2000
Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomaliesL Pavone, R Rizzo, P Pavone, et al.
Journal of Child Neurology|July 1, 1992
Trichothiodystrophy: report of a new case with severe nervous system impairmentR Rizzo, L Pavone, G Micali, et al.
Annales De Pediatrie|December 1, 1983
[Intestinal lymphangiectasis in a child with congenital hemihypertrophy]L Pavone, G Distefano, R Patanè, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1982
Increased serum phospholipids in epileptic children treated with phenobarbitoneL Pavone, G Klose, F Mollica, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1985
Twins with acardia and anencephalyL Pavone, K M Laurence, T Mattina, et al.
The Johns Hopkins Medical Journal|November 1, 1980
Farber's lipogranulomatosis: ceramidase deficiency and prolonged survival in three relativesL Pavone, H W Moser, F Mollica, et al.
Pageof 17

Showing results (81-90 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Diseases of Children (1960)|July 1, 1980
Picture of the month. Metaphyseal chondrodysplasia, Schmid typeS S Gellis, M Feingold, L Pavone, et al.
Clinical Pediatrics|April 1, 1996
Multiple sclerosis with onset at 35 months of ageM Ruggieri, A Fiumara, L M Grimaldi, et al.
American Journal of Medical Genetics|October 1, 1993
Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicismR Rizzo, L Pavone, G Micali, et al.
Acta Neurologica|August 1, 1984
Peculiar congenital myopathy in two siblings. Congenital fibre type disproportion or type II fibres hypotrophy?L Pavone, R Scelsi, F Gullotta, et al.
Journal of Child Neurology|August 2, 2000
Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomaliesL Pavone, R Rizzo, P Pavone, et al.
Journal of Child Neurology|July 1, 1992
Trichothiodystrophy: report of a new case with severe nervous system impairmentR Rizzo, L Pavone, G Micali, et al.
Annales De Pediatrie|December 1, 1983
[Intestinal lymphangiectasis in a child with congenital hemihypertrophy]L Pavone, G Distefano, R Patanè, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1982
Increased serum phospholipids in epileptic children treated with phenobarbitoneL Pavone, G Klose, F Mollica, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1985
Twins with acardia and anencephalyL Pavone, K M Laurence, T Mattina, et al.
The Johns Hopkins Medical Journal|November 1, 1980
Farber's lipogranulomatosis: ceramidase deficiency and prolonged survival in three relativesL Pavone, H W Moser, F Mollica, et al.
Pageof 17