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Achille Iolascon

Showing results (71-80 of 290) with videos related to

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American Journal of Hematology|September 7, 2018
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patientsImmacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, et al.
Clinical Chemistry|September 23, 2003
Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genesLucia Giordani, Paolo Bruzzi, Carla Lasalandra, et al.
British Journal of Haematology|November 8, 2011
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 updatePaula H B Bolton-Maggs, Jacob C Langer, Achille Iolascon, et al.
Journal of Cellular and Molecular Medicine|April 27, 2020
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastomaImmacolata Andolfo, Vito A Lasorsa, Francesco Manna, et al.
The Lancet. Oncology|February 2, 2008
Challenges in prescribing drugs for children with cancerPaolo Paolucci, Kathy Pritchard Jones, Maria del Carmen Cano Garcinuno, et al.
International Journal of Pediatric Otorhinolaryngology|April 7, 2020
Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case reportRita Malesci, Roberta Russo, Carmela Monzillo, et al.
International Journal of Molecular Sciences|August 8, 2020
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 PathwayGianluca De Rosa, Immacolata Andolfo, Roberta Marra, et al.
Pediatric Research|February 23, 2007
Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndromeMario Capasso, Rosa Anna Avvisati, Carmelo Piscopo, et al.
Blood Advances|March 23, 2022
Deferasirox-induced robust and dose-dependent reversal of anemia in a patient with variants in the TRIB2 and ABCB6 genesJulia Stomper, Paulina Richter-Pechanska, Dietmar Pfeifer, et al.
Haematologica|May 15, 2003
Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle PiastrineCarlo L Balduini, Marco Cattaneo, Fabrizio Fabris, et al.
Pageof 29

Showing results (71-80 of 290) with videos related to

Sort By:
Pageof 29
American Journal of Hematology|September 7, 2018
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patientsImmacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, et al.
Clinical Chemistry|September 23, 2003
Association of breast cancer and polymorphisms of interleukin-10 and tumor necrosis factor-alpha genesLucia Giordani, Paolo Bruzzi, Carla Lasalandra, et al.
British Journal of Haematology|November 8, 2011
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 updatePaula H B Bolton-Maggs, Jacob C Langer, Achille Iolascon, et al.
Journal of Cellular and Molecular Medicine|April 27, 2020
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastomaImmacolata Andolfo, Vito A Lasorsa, Francesco Manna, et al.
The Lancet. Oncology|February 2, 2008
Challenges in prescribing drugs for children with cancerPaolo Paolucci, Kathy Pritchard Jones, Maria del Carmen Cano Garcinuno, et al.
International Journal of Pediatric Otorhinolaryngology|April 7, 2020
Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case reportRita Malesci, Roberta Russo, Carmela Monzillo, et al.
International Journal of Molecular Sciences|August 8, 2020
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 PathwayGianluca De Rosa, Immacolata Andolfo, Roberta Marra, et al.
Pediatric Research|February 23, 2007
Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndromeMario Capasso, Rosa Anna Avvisati, Carmelo Piscopo, et al.
Blood Advances|March 23, 2022
Deferasirox-induced robust and dose-dependent reversal of anemia in a patient with variants in the TRIB2 and ABCB6 genesJulia Stomper, Paulina Richter-Pechanska, Dietmar Pfeifer, et al.
Haematologica|May 15, 2003
Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle PiastrineCarlo L Balduini, Marco Cattaneo, Fabrizio Fabris, et al.
Pageof 29