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L Pavone

Showing results (31-40 of 165) with videos related to

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Acta Geneticae Medicae Et Gemellologiae|October 1, 1972
Robins's syndrome in three children of consanguineous parents. A pedigree suggesting autosomal recessive inheritanceG Russo, F Mollica, L Pavone, et al.
Clinical Genetics|August 1, 1979
A case of cyclopia. Role of environmental factorsF Mollica, L Pavone, G Nuciforo, et al.
Minerva Medica|February 14, 1972
[Heterogeneity of muscular dystrophy]H Zellweger, L Pavone, V Ionasescu, et al.
Clinical Rheumatology|June 9, 2005
ENT Wegener's granulomatosis can hide severe central nervous system involvementB Tumiati, G Zuccoli, L Pavone, et al.
Clinical Dysmorphology|July 1, 1996
Hypertrichosis, coarse face, brachydactyly, obesity and mental retardationL Pavone, R Rizzo, M Ruggieri, et al.
American Journal of Medical Genetics|November 14, 2000
Pallister-Killian syndrome: case report with pineal tumorL Mauceri, G Sorge, G Incorpora, et al.
Acta Paediatrica Scandinavica|January 1, 1979
Immuno-deficiency in Schwartz-Jampel syndromeF Mollica, A Messina, F Stivala, et al.
Italian Journal of Neurological Sciences|December 1, 1985
Infantile spasms syndrome in monozygotic twins. A 7-year follow-upL Pavone, F Mollica, G Incorpora, et al.
Pediatrics|June 1, 1972
Hemolytic crises of favism in Sicilian females heterozygous for G-6-PD deficiencyG Russo, F Mollica, L Pavone, et al.
Neuropediatrics|November 1, 1986
Hydrocephalus, lissencephaly, ocular abnormalities and congenital muscular dystrophy. A Warburg syndrome variant?L Pavone, F Gullotta, S Grasso, et al.
Pageof 17

Showing results (31-40 of 165) with videos related to

Sort By:
Pageof 17
Acta Geneticae Medicae Et Gemellologiae|October 1, 1972
Robins's syndrome in three children of consanguineous parents. A pedigree suggesting autosomal recessive inheritanceG Russo, F Mollica, L Pavone, et al.
Clinical Genetics|August 1, 1979
A case of cyclopia. Role of environmental factorsF Mollica, L Pavone, G Nuciforo, et al.
Minerva Medica|February 14, 1972
[Heterogeneity of muscular dystrophy]H Zellweger, L Pavone, V Ionasescu, et al.
Clinical Rheumatology|June 9, 2005
ENT Wegener's granulomatosis can hide severe central nervous system involvementB Tumiati, G Zuccoli, L Pavone, et al.
Clinical Dysmorphology|July 1, 1996
Hypertrichosis, coarse face, brachydactyly, obesity and mental retardationL Pavone, R Rizzo, M Ruggieri, et al.
American Journal of Medical Genetics|November 14, 2000
Pallister-Killian syndrome: case report with pineal tumorL Mauceri, G Sorge, G Incorpora, et al.
Acta Paediatrica Scandinavica|January 1, 1979
Immuno-deficiency in Schwartz-Jampel syndromeF Mollica, A Messina, F Stivala, et al.
Italian Journal of Neurological Sciences|December 1, 1985
Infantile spasms syndrome in monozygotic twins. A 7-year follow-upL Pavone, F Mollica, G Incorpora, et al.
Pediatrics|June 1, 1972
Hemolytic crises of favism in Sicilian females heterozygous for G-6-PD deficiencyG Russo, F Mollica, L Pavone, et al.
Neuropediatrics|November 1, 1986
Hydrocephalus, lissencephaly, ocular abnormalities and congenital muscular dystrophy. A Warburg syndrome variant?L Pavone, F Gullotta, S Grasso, et al.
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