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L Luzzatto

Showing results (141-150 of 259) with videos related to

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The Journal of Obstetrics and Gynaecology of the British Commonwealth|May 1, 1972
Pregnancy in homozygous sickle-cell anaemiaJ P Hendrickse, E J Watson-Williams, L Luzzatto, et al.
Blood|December 15, 1992
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangementsI Dokal, J Bungey, P Williamson, et al.
The New England Journal of Medicine|November 9, 1995
Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.
British Journal of Haematology|September 1, 1995
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD geneA Rovira, T Vulliamy, M A Pujades, et al.
Human Genetics|April 1, 1993
G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish JewsA Oppenheim, C L Jury, D Rund, et al.
Gene|September 16, 1996
High-level regulated expression of the human G6PD gene in transgenic miceC M Corcoran, P Fraser, G Martini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Evaluation of iron overload in thalassemia]A Piga, S Davico, M Magliano, et al.
European Journal of Haematology|April 1, 1988
High-dose desferrioxamine as a cause of growth failure in thalassemic patientsA Piga, L Luzzatto, P Capalbo, et al.
American Journal of Human Genetics|September 1, 1977
Response to Nance letterG Battistuzzi, G J Esan, F A Fasuan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.
Pageof 26

Showing results (141-150 of 259) with videos related to

Sort By:
Pageof 26
The Journal of Obstetrics and Gynaecology of the British Commonwealth|May 1, 1972
Pregnancy in homozygous sickle-cell anaemiaJ P Hendrickse, E J Watson-Williams, L Luzzatto, et al.
Blood|December 15, 1992
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangementsI Dokal, J Bungey, P Williamson, et al.
The New England Journal of Medicine|November 9, 1995
Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.
British Journal of Haematology|September 1, 1995
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD geneA Rovira, T Vulliamy, M A Pujades, et al.
Human Genetics|April 1, 1993
G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish JewsA Oppenheim, C L Jury, D Rund, et al.
Gene|September 16, 1996
High-level regulated expression of the human G6PD gene in transgenic miceC M Corcoran, P Fraser, G Martini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Evaluation of iron overload in thalassemia]A Piga, S Davico, M Magliano, et al.
European Journal of Haematology|April 1, 1988
High-dose desferrioxamine as a cause of growth failure in thalassemic patientsA Piga, L Luzzatto, P Capalbo, et al.
American Journal of Human Genetics|September 1, 1977
Response to Nance letterG Battistuzzi, G J Esan, F A Fasuan, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuriaP Hillmen, M Bessler, P J Mason, et al.
Pageof 26