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Fernando F Costa

Showing results (121-130 of 154) with videos related to

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Scientific Reports|July 28, 2019
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergencePedro R S Cruz, Galina Ananina, Vera Lucia Gil-da-Silva-Lopes, et al.
Nuclear Medicine Communications|November 8, 2006
51Cr-EDTA measurements of the glomerular filtration rate in patients with sickle cell anaemia and minor renal damageFabiana B Barros, Carmen S P Lima, Allan O Santos, et al.
British Journal of Haematology|February 19, 2016
Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 lociFlávia C Leonardo, Ana F Brugnerotto, Igor F Domingos, et al.
Archives of Biochemistry and Biophysics|January 17, 2012
Hb S-São Paulo: a new sickling hemoglobin with stable polymers and decreased oxygen affinitySusan E D C Jorge, Ariel A Petruk, Elza M Kimura, et al.
The Journal of Clinical Investigation|January 27, 2015
Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminusMarta Byrska-Bishop, Daniel VanDorn, Amy E Campbell, et al.
British Journal of Haematology|November 12, 2019
Association between ANXA2*5681 polymorphism (rs7170178) and osteonecrosis in haemoglobin SS-genotyped patientsDiego A Pereira-Martins, Juan L Coelho-Silva, Igor F Domingos, et al.
European Journal of Haematology|June 17, 2009
Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta122 (GH5) Phe-->Ser], a probable case of germ line mutation, and Hb Olinda [beta22 (B4) - 25 (B7)], a deletion of a 12 base-pair sequenceMarcos A C Bezerra, Dulcinéia M Albuquerque, Magnun N N Santos, et al.
Blood|July 15, 2016
A randomized trial of amlodipine in addition to standard chelation therapy in patients with thalassemia majorJuliano L Fernandes, Sandra R Loggetto, Monica P A Veríssimo, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Association of genetic variants rs641153 (<i>CFB</i>), rs2230199 (<i>C3</i>), and rs1410996 (<i>CFH</i>) with age-related macular degeneration in a Brazilian populationJamil M Neto, Marina Gm Viturino, Galina Ananina, et al.
Annals of Hematology|February 5, 2014
Influence of the βs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemiaIgor F Domingos, Diego A Falcão, Betania L Hatzlhofer, et al.
Pageof 16

Showing results (121-130 of 154) with videos related to

Sort By:
Pageof 16
Scientific Reports|July 28, 2019
Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergencePedro R S Cruz, Galina Ananina, Vera Lucia Gil-da-Silva-Lopes, et al.
Nuclear Medicine Communications|November 8, 2006
51Cr-EDTA measurements of the glomerular filtration rate in patients with sickle cell anaemia and minor renal damageFabiana B Barros, Carmen S P Lima, Allan O Santos, et al.
British Journal of Haematology|February 19, 2016
Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 lociFlávia C Leonardo, Ana F Brugnerotto, Igor F Domingos, et al.
Archives of Biochemistry and Biophysics|January 17, 2012
Hb S-São Paulo: a new sickling hemoglobin with stable polymers and decreased oxygen affinitySusan E D C Jorge, Ariel A Petruk, Elza M Kimura, et al.
The Journal of Clinical Investigation|January 27, 2015
Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminusMarta Byrska-Bishop, Daniel VanDorn, Amy E Campbell, et al.
British Journal of Haematology|November 12, 2019
Association between ANXA2*5681 polymorphism (rs7170178) and osteonecrosis in haemoglobin SS-genotyped patientsDiego A Pereira-Martins, Juan L Coelho-Silva, Igor F Domingos, et al.
European Journal of Haematology|June 17, 2009
Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta122 (GH5) Phe-->Ser], a probable case of germ line mutation, and Hb Olinda [beta22 (B4) - 25 (B7)], a deletion of a 12 base-pair sequenceMarcos A C Bezerra, Dulcinéia M Albuquerque, Magnun N N Santos, et al.
Blood|July 15, 2016
A randomized trial of amlodipine in addition to standard chelation therapy in patients with thalassemia majorJuliano L Fernandes, Sandra R Loggetto, Monica P A Veríssimo, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Association of genetic variants rs641153 (<i>CFB</i>), rs2230199 (<i>C3</i>), and rs1410996 (<i>CFH</i>) with age-related macular degeneration in a Brazilian populationJamil M Neto, Marina Gm Viturino, Galina Ananina, et al.
Annals of Hematology|February 5, 2014
Influence of the βs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemiaIgor F Domingos, Diego A Falcão, Betania L Hatzlhofer, et al.
Pageof 16