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Sule Unal

Showing results (91-100 of 105) with videos related to

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Hemasphere|July 16, 2024
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemiaAchille Iolascon, Immacolata Andolfo, Roberta Russo, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
Blood|February 28, 2022
A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemiaDavid C Rees, Yurdanur Kilinc, Selma Unal, et al.
Blood|January 5, 2013
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine productionSamuel C C Chiang, Jakob Theorell, Miriam Entesarian, et al.
Mediterranean Journal of Hematology and Infectious Diseases|May 15, 2026
A Descriptive Preanalytical Survey of Procedures Followed for the Screening of Glucose Dysregulation in Thalassemia Centers: Implications for Clinical Practice and Call for HarmonizationVincenzo de Sanctis, Shahina Daar, Ploutarchos Tzoulis, et al.
Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.
Journal of Hepatology|March 19, 2026
Characterization of ferroportin disease and SLC40A1-related hemochromatosis - Results from the EASL non-HFE registryMaria Rosina Troppmair, Andrea Ricci, Stefania Scarlini, et al.
Blood|February 25, 2022
HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemiaMarie-Françoise O'Donohue, Lydie Da Costa, Marco Lezzerini, et al.
European Journal of Haematology|March 31, 2024
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysisEsra Isik, Yesim Aydinok, Canan Albayrak, et al.
Mediterranean Journal of Hematology and Infectious Diseases|January 20, 2025
A Multicenter ICET-A Survey on Adherence to Annual Oral Glucose Tolerance Test (OGTT) Screening in Transfusion-Dependent Thalassemia (TDT) Patients - The Expert Clinicians' Opinion on Factors Influencing the Adherence and on Alternative Strategies for Adherence OptimizationVincenzo de Sanctis, Duran Canatan, Shahina Daar, et al.
Pageof 11

Showing results (91-100 of 105) with videos related to

Sort By:
Pageof 11
Hemasphere|July 16, 2024
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemiaAchille Iolascon, Immacolata Andolfo, Roberta Russo, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
Blood|February 28, 2022
A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemiaDavid C Rees, Yurdanur Kilinc, Selma Unal, et al.
Blood|January 5, 2013
Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine productionSamuel C C Chiang, Jakob Theorell, Miriam Entesarian, et al.
Mediterranean Journal of Hematology and Infectious Diseases|May 15, 2026
A Descriptive Preanalytical Survey of Procedures Followed for the Screening of Glucose Dysregulation in Thalassemia Centers: Implications for Clinical Practice and Call for HarmonizationVincenzo de Sanctis, Shahina Daar, Ploutarchos Tzoulis, et al.
Genome Medicine|December 20, 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosisBianca Tesi, Kristina Lagerstedt-Robinson, Samuel C C Chiang, et al.
Journal of Hepatology|March 19, 2026
Characterization of ferroportin disease and SLC40A1-related hemochromatosis - Results from the EASL non-HFE registryMaria Rosina Troppmair, Andrea Ricci, Stefania Scarlini, et al.
Blood|February 25, 2022
HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemiaMarie-Françoise O'Donohue, Lydie Da Costa, Marco Lezzerini, et al.
European Journal of Haematology|March 31, 2024
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysisEsra Isik, Yesim Aydinok, Canan Albayrak, et al.
Mediterranean Journal of Hematology and Infectious Diseases|January 20, 2025
A Multicenter ICET-A Survey on Adherence to Annual Oral Glucose Tolerance Test (OGTT) Screening in Transfusion-Dependent Thalassemia (TDT) Patients - The Expert Clinicians' Opinion on Factors Influencing the Adherence and on Alternative Strategies for Adherence OptimizationVincenzo de Sanctis, Duran Canatan, Shahina Daar, et al.
Pageof 11