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Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
January 22, 2000
Altered N-glycosylation in macrophage x melanoma fusion hybrids
J 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 cohort
P Fortunato, A Pagliazzi, S Bargiacchi, et al.
Contributions to Nephrology
|
November 2, 2001
Anderson-Fabry disease: molecular analysis and clinical manifestations in three Italian families
F 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 pigmentosa
F 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 gene
F 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 mechanism
S 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 occlusion
M Becatti, R Marcucci, A M Gori, et al.
Haematologica
|
March 1, 1996
Familial AL-amyloidosis in three Italian siblings
A Miliani, F Bergesio, M Salvadori, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 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 hybrids
J 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 cohort
P Fortunato, A Pagliazzi, S Bargiacchi, et al.
Contributions to Nephrology
|
November 2, 2001
Anderson-Fabry disease: molecular analysis and clinical manifestations in three Italian families
F 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 pigmentosa
F 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 gene
F 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 mechanism
S 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 occlusion
M Becatti, R Marcucci, A M Gori, et al.
Haematologica
|
March 1, 1996
Familial AL-amyloidosis in three Italian siblings
A Miliani, F Bergesio, M Salvadori, et al.
Page
of 4