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Showing results (31-40 of 39) with videos related to

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Cellular and Molecular Biology (Noisy-Le-Grand, France)|January 22, 2000
Altered N-glycosylation in macrophage x melanoma fusion hybridsJ M Pawelek, A K Chakraborty, M L Rachkovsky, et al.
Ophthalmic Genetics|November 15, 2022
X-linked retinoschisis: mutation spectrum and genotype-phenotype relationship in an Italian pediatric cohortP Fortunato, A Pagliazzi, S Bargiacchi, et al.
Contributions to Nephrology|November 2, 2001
Anderson-Fabry disease: molecular analysis and clinical manifestations in three Italian familiesF Torricelli, F Martinelli, E Pelo, et al.
Contributions to Nephrology|January 1, 1997
Anderson-Fabry disease. Three families detected in 2 years: unusual occurrence or good interdisciplinary collaboration?F Martinelli, F Bergesio, R Piperno, et al.
Archivos De La Sociedad Espanola De Oftalmologia|October 9, 2023
The suprachoroidal space in patients affected by retinitis pigmentosaF Giansanti, G Virgili, A Sodi, et al.
The British Journal of Ophthalmology|August 16, 2008
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 geneF Testa, S Rossi, I Passerini, et al.
Pigment Cell Research|January 7, 1999
Melanoma x macrophage fusion hybrids acquire increased melanogenesis and metastatic potential: altered N-glycosylation as an underlying mechanismS A Sodi, A K Chakraborty, J T Platt, et al.
Journal of Thrombosis and Haemostasis : JTH|August 26, 2016
Erythrocyte oxidative stress is associated with cell deformability in patients with retinal vein occlusionM Becatti, R Marcucci, A M Gori, et al.
Haematologica|March 1, 1996
Familial AL-amyloidosis in three Italian siblingsA Miliani, F Bergesio, M Salvadori, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|January 22, 2000
Altered N-glycosylation in macrophage x melanoma fusion hybridsJ M Pawelek, A K Chakraborty, M L Rachkovsky, et al.
Ophthalmic Genetics|November 15, 2022
X-linked retinoschisis: mutation spectrum and genotype-phenotype relationship in an Italian pediatric cohortP Fortunato, A Pagliazzi, S Bargiacchi, et al.
Contributions to Nephrology|November 2, 2001
Anderson-Fabry disease: molecular analysis and clinical manifestations in three Italian familiesF Torricelli, F Martinelli, E Pelo, et al.
Contributions to Nephrology|January 1, 1997
Anderson-Fabry disease. Three families detected in 2 years: unusual occurrence or good interdisciplinary collaboration?F Martinelli, F Bergesio, R Piperno, et al.
Archivos De La Sociedad Espanola De Oftalmologia|October 9, 2023
The suprachoroidal space in patients affected by retinitis pigmentosaF Giansanti, G Virgili, A Sodi, et al.
The British Journal of Ophthalmology|August 16, 2008
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 geneF Testa, S Rossi, I Passerini, et al.
Pigment Cell Research|January 7, 1999
Melanoma x macrophage fusion hybrids acquire increased melanogenesis and metastatic potential: altered N-glycosylation as an underlying mechanismS A Sodi, A K Chakraborty, J T Platt, et al.
Journal of Thrombosis and Haemostasis : JTH|August 26, 2016
Erythrocyte oxidative stress is associated with cell deformability in patients with retinal vein occlusionM Becatti, R Marcucci, A M Gori, et al.
Haematologica|March 1, 1996
Familial AL-amyloidosis in three Italian siblingsA Miliani, F Bergesio, M Salvadori, et al.
Pageof 4