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Achille Iolascon

Showing results (221-230 of 251) with videos related to

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Genes|July 2, 2021
The <i>TNFRSF13C</i> H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern ItalyRoberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, et al.
Hemasphere|June 8, 2026
EHA Recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathiesMariane de Montalembert, Maria D Cappellini, Achille Iolascon, et al.
Plos One|March 25, 2009
MicroRNA-199b-5p impairs cancer stem cells through negative regulation of HES1 in medulloblastomaLivia Garzia, Immacolata Andolfo, Emilio Cusanelli, et al.
Expert Opinion on Pharmacotherapy|August 19, 2007
Pharmacogenetics and paediatric drug development: issues and consequences to labelling and dosing recommendationsElke H J Krekels, John N van den Anker, Paola Baiardi, et al.
International Journal of Molecular Sciences|June 2, 2021
Regulatory Noncoding and Predicted Pathogenic Coding Variants of <i>CCR5</i> Predispose to Severe COVID-19Sueva Cantalupo, Vito Alessandro Lasorsa, Roberta Russo, et al.
Antioxidants & Redox Signaling|August 11, 2017
Peroxiredoxin-2: A Novel Regulator of Iron Homeostasis in Ineffective ErythropoiesisAlessandro Matte, Luigia De Falco, Enrica Federti, et al.
Blood Advances|April 22, 2026
Clinical variability of ATP11C-related hemolytic anemia: expanding the phenotypic and diagnostic spectrumVanessa D'Onofrio, Federica Maria Esposito, Roberta Marra, et al.
American Journal of Hematology|September 1, 2021
Recommendations for diagnosis and treatment of methemoglobinemiaAchille Iolascon, Paola Bianchi, Immacolata Andolfo, et al.
Haematologica|May 28, 2017
Recommendations regarding splenectomy in hereditary hemolytic anemiasAchille Iolascon, Immacolata Andolfo, Wilma Barcellini, et al.
American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.
Pageof 26

Showing results (221-230 of 251) with videos related to

Sort By:
Pageof 26
Genes|July 2, 2021
The <i>TNFRSF13C</i> H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern ItalyRoberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, et al.
Hemasphere|June 8, 2026
EHA Recommendations for preconceptual and antenatal screening and prenatal diagnosis for hemoglobinopathiesMariane de Montalembert, Maria D Cappellini, Achille Iolascon, et al.
Plos One|March 25, 2009
MicroRNA-199b-5p impairs cancer stem cells through negative regulation of HES1 in medulloblastomaLivia Garzia, Immacolata Andolfo, Emilio Cusanelli, et al.
Expert Opinion on Pharmacotherapy|August 19, 2007
Pharmacogenetics and paediatric drug development: issues and consequences to labelling and dosing recommendationsElke H J Krekels, John N van den Anker, Paola Baiardi, et al.
International Journal of Molecular Sciences|June 2, 2021
Regulatory Noncoding and Predicted Pathogenic Coding Variants of <i>CCR5</i> Predispose to Severe COVID-19Sueva Cantalupo, Vito Alessandro Lasorsa, Roberta Russo, et al.
Antioxidants & Redox Signaling|August 11, 2017
Peroxiredoxin-2: A Novel Regulator of Iron Homeostasis in Ineffective ErythropoiesisAlessandro Matte, Luigia De Falco, Enrica Federti, et al.
Blood Advances|April 22, 2026
Clinical variability of ATP11C-related hemolytic anemia: expanding the phenotypic and diagnostic spectrumVanessa D'Onofrio, Federica Maria Esposito, Roberta Marra, et al.
American Journal of Hematology|September 1, 2021
Recommendations for diagnosis and treatment of methemoglobinemiaAchille Iolascon, Paola Bianchi, Immacolata Andolfo, et al.
Haematologica|May 28, 2017
Recommendations regarding splenectomy in hereditary hemolytic anemiasAchille Iolascon, Immacolata Andolfo, Wilma Barcellini, et al.
American Journal of Human Genetics|November 9, 2010
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemiaLionel Arnaud, Carole Saison, Virginie Helias, et al.
Pageof 26