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Lucio Luzzatto

Showing results (101-110 of 140) with videos related to

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Oncotarget|April 21, 2016
Thin and thick primary cutaneous melanomas reveal distinct patterns of somatic copy number alterationsValentina Montagnani, Matteo Benelli, Alessandro Apollo, et al.
Blood|June 16, 2005
Patients with paroxysmal nocturnal hemoglobinuria have a high frequency of peripheral-blood T cells expressing activating isoforms of inhibiting superfamily receptorsAlessandro Poggi, Simone Negrini, Maria Raffaella Zocchi, et al.
American Journal of Hematology|July 11, 2025
Novel ADAMTS13 Mutation in a Patient With Congenital TTP Diagnosed in PregnancyWilliam Frank Mawalla, Clara Chamba, Ahlam Nasser, et al.
Case Reports in Hematology|July 24, 2018
Limited Exchange Transfusion Can Be Very Beneficial in Sickle Cell Anemia with Acute Chest Syndrome: A Case Report from TanzaniaClara Chamba, Hamisa Iddy, Erius Tebuka, et al.
Human Genomics|May 10, 2021
COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policyGiuseppe Novelli, Michela Biancolella, Ruty Mehrian-Shai, et al.
Future Microbiology|October 10, 2019
Tafenoquine for the prophylaxis, treatment and elimination of malaria: eagerness must meet prudenceFernando Val, Fabio Tm Costa, Liam King, et al.
The EMBO Journal|August 10, 2002
Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethalLetizia Longo, Olga Camacho Vanegas, Meghavi Patel, et al.
Blood|July 30, 2005
Diagnosis and management of paroxysmal nocturnal hemoglobinuriaCharles Parker, Mitsuhiro Omine, Stephen Richards, et al.
Plos Neglected Tropical Diseases|September 8, 2021
Dynamics of G6PD activity in patients receiving weekly primaquine for therapy of Plasmodium vivax malariaWalter R J Taylor, Saorin Kim, Sim Kheng, et al.
American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
Pageof 14

Showing results (101-110 of 140) with videos related to

Sort By:
Pageof 14
Oncotarget|April 21, 2016
Thin and thick primary cutaneous melanomas reveal distinct patterns of somatic copy number alterationsValentina Montagnani, Matteo Benelli, Alessandro Apollo, et al.
Blood|June 16, 2005
Patients with paroxysmal nocturnal hemoglobinuria have a high frequency of peripheral-blood T cells expressing activating isoforms of inhibiting superfamily receptorsAlessandro Poggi, Simone Negrini, Maria Raffaella Zocchi, et al.
American Journal of Hematology|July 11, 2025
Novel ADAMTS13 Mutation in a Patient With Congenital TTP Diagnosed in PregnancyWilliam Frank Mawalla, Clara Chamba, Ahlam Nasser, et al.
Case Reports in Hematology|July 24, 2018
Limited Exchange Transfusion Can Be Very Beneficial in Sickle Cell Anemia with Acute Chest Syndrome: A Case Report from TanzaniaClara Chamba, Hamisa Iddy, Erius Tebuka, et al.
Human Genomics|May 10, 2021
COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policyGiuseppe Novelli, Michela Biancolella, Ruty Mehrian-Shai, et al.
Future Microbiology|October 10, 2019
Tafenoquine for the prophylaxis, treatment and elimination of malaria: eagerness must meet prudenceFernando Val, Fabio Tm Costa, Liam King, et al.
The EMBO Journal|August 10, 2002
Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethalLetizia Longo, Olga Camacho Vanegas, Meghavi Patel, et al.
Blood|July 30, 2005
Diagnosis and management of paroxysmal nocturnal hemoglobinuriaCharles Parker, Mitsuhiro Omine, Stephen Richards, et al.
Plos Neglected Tropical Diseases|September 8, 2021
Dynamics of G6PD activity in patients receiving weekly primaquine for therapy of Plasmodium vivax malariaWalter R J Taylor, Saorin Kim, Sim Kheng, et al.
American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
Pageof 14