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American Journal of Diseases of Children (1960)
|
July 1, 1980
Picture of the month. Metaphyseal chondrodysplasia, Schmid type
S S Gellis, M Feingold, L Pavone, et al.
Clinical Pediatrics
|
April 1, 1996
Multiple sclerosis with onset at 35 months of age
M Ruggieri, A Fiumara, L M Grimaldi, et al.
American Journal of Medical Genetics
|
October 1, 1993
Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicism
R 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 anomalies
L Pavone, R Rizzo, P Pavone, et al.
Journal of Child Neurology
|
July 1, 1992
Trichothiodystrophy: report of a new case with severe nervous system impairment
R 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 phenobarbitone
L Pavone, G Klose, F Mollica, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1985
Twins with acardia and anencephaly
L 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 relatives
L Pavone, H W Moser, F Mollica, et al.
Page
of 17
Search research articles
Search
Showing results (81-90 of 165) with videos related to
Sort By:
Page
of 17
American Journal of Diseases of Children (1960)
|
July 1, 1980
Picture of the month. Metaphyseal chondrodysplasia, Schmid type
S S Gellis, M Feingold, L Pavone, et al.
Clinical Pediatrics
|
April 1, 1996
Multiple sclerosis with onset at 35 months of age
M Ruggieri, A Fiumara, L M Grimaldi, et al.
American Journal of Medical Genetics
|
October 1, 1993
Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicism
R 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 anomalies
L Pavone, R Rizzo, P Pavone, et al.
Journal of Child Neurology
|
July 1, 1992
Trichothiodystrophy: report of a new case with severe nervous system impairment
R 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 phenobarbitone
L Pavone, G Klose, F Mollica, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1985
Twins with acardia and anencephaly
L 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 relatives
L Pavone, H W Moser, F Mollica, et al.
Page
of 17