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Elisa Fermo

Showing results (81-90 of 93) with videos related to

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American Journal of Hematology|September 12, 2023
Immunomodulatory cytokines and clonal dynamics in low-risk myelodysplastic syndromes patients treated with luspaterceptBruno Fattizzo, Alfredo Marchetti, Anna Zaninoni, et al.
Scientific Reports|May 13, 2017
'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulationElisa Fermo, Anna Bogdanova, Polina Petkova-Kirova, et al.
Clinical Biochemistry|February 25, 2021
Six novel variants in the PKLR gene associated with pyruvate kinase deficiency in Argentinian patientsBerenice Milanesio, Carolina Pepe, Lucas A Defelipe, et al.
Hemasphere|January 12, 2026
Hypomorphic <i>ATP11c</i> is a novel regulator of decreased efficacy of transfused red blood cells in humans and miceJames C Zimring, Ariel M Hay, Monika Dzieciatkowska, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 11, 2019
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivoBartholomew P Roland, Kristen R Richards, Stacy L Hrizo, et al.
Hemasphere|June 10, 2022
The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice PaperNoémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
British Journal of Haematology|June 6, 2022
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice PaperNoémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
American Journal of Hematology|October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo, Bertil Glader, et al.
Haematologica|June 2, 2016
Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblastsTimothy J Satchwell, Amanda J Bell, Bethan R Hawley, et al.
Hemasphere|November 22, 2021
Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of MethemoglobinemiaAchille Iolascon, Immacolata Andolfo, Roberta Russo, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
American Journal of Hematology|September 12, 2023
Immunomodulatory cytokines and clonal dynamics in low-risk myelodysplastic syndromes patients treated with luspaterceptBruno Fattizzo, Alfredo Marchetti, Anna Zaninoni, et al.
Scientific Reports|May 13, 2017
'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulationElisa Fermo, Anna Bogdanova, Polina Petkova-Kirova, et al.
Clinical Biochemistry|February 25, 2021
Six novel variants in the PKLR gene associated with pyruvate kinase deficiency in Argentinian patientsBerenice Milanesio, Carolina Pepe, Lucas A Defelipe, et al.
Hemasphere|January 12, 2026
Hypomorphic <i>ATP11c</i> is a novel regulator of decreased efficacy of transfused red blood cells in humans and miceJames C Zimring, Ariel M Hay, Monika Dzieciatkowska, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 11, 2019
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivoBartholomew P Roland, Kristen R Richards, Stacy L Hrizo, et al.
Hemasphere|June 10, 2022
The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice PaperNoémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
British Journal of Haematology|June 6, 2022
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice PaperNoémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
American Journal of Hematology|October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo, Bertil Glader, et al.
Haematologica|June 2, 2016
Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblastsTimothy J Satchwell, Amanda J Bell, Bethan R Hawley, et al.
Hemasphere|November 22, 2021
Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of MethemoglobinemiaAchille Iolascon, Immacolata Andolfo, Roberta Russo, et al.
Pageof 10