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L Pavone

Showing results (1-10 of 165) with videos related to

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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[The pathogenesis of cerebral malformations]L Pavone
Minerva Pediatrica|March 1, 1991
[Mental retardation. The nosographic picture of mental retardation]L Pavone
Journal of Child Neurology|November 4, 2000
Hypomelanosis of Ito: clinical syndrome or just phenotype?M Ruggieri, L Pavone
Acta Paediatrica Scandinavica|March 1, 1976
Hyperprolinaemia: a disease which does not need treatment?F Mollica, L Pavone
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1985
[Therapy of infantile spasms (West syndrome) with sodium dipropylacetate]L Pavone, G Incorpora
American Journal of Medical Genetics|December 4, 1995
Autosomal-recessive microcephaly in two siblings, one with normal IQ and both with protruding mandible, small ears, and curved noseR Rizzo, L Pavone
Journal of Inherited Metabolic Disease|January 1, 1986
Niemann-Pick disease type B: clinical signs and follow-up of a new caseL Pavone, A Fiumara, M LaRosa
Pediatrics|August 1, 1971
Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian familyF Mollica, L Pavone, I Antener
Monographs in Human Genetics|January 1, 1972
Familial hyperprolinemia without mental retardation and hereditary nephropathyF Mollica, L Pavone, I Antener
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1975
[Congenital hereditary corneal dystrophy associated with various extraoculary anomalies]A Scialfa, F Mollica, L Pavone
Pageof 17

Showing results (1-10 of 165) with videos related to

Sort By:
Pageof 17
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[The pathogenesis of cerebral malformations]L Pavone
Minerva Pediatrica|March 1, 1991
[Mental retardation. The nosographic picture of mental retardation]L Pavone
Journal of Child Neurology|November 4, 2000
Hypomelanosis of Ito: clinical syndrome or just phenotype?M Ruggieri, L Pavone
Acta Paediatrica Scandinavica|March 1, 1976
Hyperprolinaemia: a disease which does not need treatment?F Mollica, L Pavone
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1985
[Therapy of infantile spasms (West syndrome) with sodium dipropylacetate]L Pavone, G Incorpora
American Journal of Medical Genetics|December 4, 1995
Autosomal-recessive microcephaly in two siblings, one with normal IQ and both with protruding mandible, small ears, and curved noseR Rizzo, L Pavone
Journal of Inherited Metabolic Disease|January 1, 1986
Niemann-Pick disease type B: clinical signs and follow-up of a new caseL Pavone, A Fiumara, M LaRosa
Pediatrics|August 1, 1971
Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian familyF Mollica, L Pavone, I Antener
Monographs in Human Genetics|January 1, 1972
Familial hyperprolinemia without mental retardation and hereditary nephropathyF Mollica, L Pavone, I Antener
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1975
[Congenital hereditary corneal dystrophy associated with various extraoculary anomalies]A Scialfa, F Mollica, L Pavone
Pageof 17