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P Simi

Showing results (11-20 of 40) with videos related to

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Hormone Research|September 6, 2000
Volumetric bone mineral density in young women with Turner's syndrome treated with estrogens or estrogens plus growth hormoneS Bertelloni, L Cinquanta, G I Baroncelli, et al.
Contributions to Nephrology|November 2, 2001
Nonsense mutation in exon 2 of the alpha-galactosidase A gene in a patient with Fabry diseaseE Manni, A Fogli, F Baldinotti, et al.
European Journal of Clinical Investigation|March 18, 2004
Adjunctive chromosomal abnormalities in Philadelphia-negative cells of CML patients treated with ImatinibG Cervetti, S Galimberti, R Fazzi, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 7, 2010
A girl with tomboy behavior: lesson from misdiagnosis in a baby with ambiguous genitaliaE Dati, F Baldinotti, M E Conidi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 23, 2000
Central precocious puberty in 48,XXYY Klinefelter syndrome variantS Bertelloni, R Battini, G I Baroncelli, et al.
Cancer Genetics and Cytogenetics|April 1, 1990
Correlation between cytogenetic and histopathological findings in 65 human meningiomasR Casalone, P Simi, P Granata, et al.
Pathologica|January 1, 1983
[Complex chromosome translocation in a case of congenital monocytic leukemia]P Simi, E Tarantino, P Macchia, et al.
Leukemia Research|August 1, 1997
The effect of cytokines, including IL4, IL7, stem cell factor, insulin-like growth factor on childhood acute lymphoblastic leukemiaR Consolini, A Legitimo, M Cattani, et al.
The European Respiratory Journal|June 2, 2010
New DNAH11 mutations in primary ciliary dyskinesia with normal axonemal ultrastructureM Pifferi, A Michelucci, M E Conidi, et al.
Minerva Pediatrica|March 3, 2004
Female phenotype at birth and postnatal masculinization, during the first months of life, associated with transient 5 alpha-reductase 2 deficiency in a preterm infant. A timing defect syndrome?M Vuerich, P Ghirri, I Merusi, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Hormone Research|September 6, 2000
Volumetric bone mineral density in young women with Turner's syndrome treated with estrogens or estrogens plus growth hormoneS Bertelloni, L Cinquanta, G I Baroncelli, et al.
Contributions to Nephrology|November 2, 2001
Nonsense mutation in exon 2 of the alpha-galactosidase A gene in a patient with Fabry diseaseE Manni, A Fogli, F Baldinotti, et al.
European Journal of Clinical Investigation|March 18, 2004
Adjunctive chromosomal abnormalities in Philadelphia-negative cells of CML patients treated with ImatinibG Cervetti, S Galimberti, R Fazzi, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|January 7, 2010
A girl with tomboy behavior: lesson from misdiagnosis in a baby with ambiguous genitaliaE Dati, F Baldinotti, M E Conidi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 23, 2000
Central precocious puberty in 48,XXYY Klinefelter syndrome variantS Bertelloni, R Battini, G I Baroncelli, et al.
Cancer Genetics and Cytogenetics|April 1, 1990
Correlation between cytogenetic and histopathological findings in 65 human meningiomasR Casalone, P Simi, P Granata, et al.
Pathologica|January 1, 1983
[Complex chromosome translocation in a case of congenital monocytic leukemia]P Simi, E Tarantino, P Macchia, et al.
Leukemia Research|August 1, 1997
The effect of cytokines, including IL4, IL7, stem cell factor, insulin-like growth factor on childhood acute lymphoblastic leukemiaR Consolini, A Legitimo, M Cattani, et al.
The European Respiratory Journal|June 2, 2010
New DNAH11 mutations in primary ciliary dyskinesia with normal axonemal ultrastructureM Pifferi, A Michelucci, M E Conidi, et al.
Minerva Pediatrica|March 3, 2004
Female phenotype at birth and postnatal masculinization, during the first months of life, associated with transient 5 alpha-reductase 2 deficiency in a preterm infant. A timing defect syndrome?M Vuerich, P Ghirri, I Merusi, et al.
Pageof 4