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Achille Iolascon

Showing results (161-170 of 290) with videos related to

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NPJ Microgravity|January 27, 2026
Label-free blood cell separation for space health monitoring using a portable blast cell biochipMartina Mugnano, Vincenza Cerbone, Massimiliano Maria Villone, et al.
American Journal of Hematology|July 17, 2015
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)Immacolata Andolfo, Roberta Russo, Francesco Manna, et al.
HLA|May 15, 2024
Exploring the role of HLA variants in neuroblastoma susceptibility through whole exome sequencingFerdinando Bonfiglio, Vito Alessandro Lasorsa, Vincenzo Aievola, et al.
Carcinogenesis|October 3, 2017
Kinome expression profiling of human neuroblastoma tumors identifies potential drug targets for ultra high-risk patientsRoberta Russo, Flora Cimmino, Lucia Pezone, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
American Journal of Hematology|March 7, 2023
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriersValeria Maria Pinto, Roberta Russo, Sabrina Quintino, et al.
Oncotarget|June 29, 2016
A comprehensive characterization of rare mitochondrial DNA variants in neuroblastomaFrancesco Maria Calabrese, Rosanna Clima, Piero Pignataro, et al.
Hemoglobin|December 13, 2019
A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek FamilyAlexandros Makis, Ioannis Georgiou, Jan Traeger-Synodinos, et al.
Nephron. Physiology|December 29, 2006
Characterization of two novel missense mutations in the AQP2 gene causing nephrogenic diabetes insipidusAchille Iolascon, Veruska Aglio, Grazia Tamma, et al.
Haematologica|August 1, 2009
A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesisAchille Iolascon, Luigia De Falco, Franck Borgese, et al.
Pageof 29

Showing results (161-170 of 290) with videos related to

Sort By:
Pageof 29
NPJ Microgravity|January 27, 2026
Label-free blood cell separation for space health monitoring using a portable blast cell biochipMartina Mugnano, Vincenza Cerbone, Massimiliano Maria Villone, et al.
American Journal of Hematology|July 17, 2015
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)Immacolata Andolfo, Roberta Russo, Francesco Manna, et al.
HLA|May 15, 2024
Exploring the role of HLA variants in neuroblastoma susceptibility through whole exome sequencingFerdinando Bonfiglio, Vito Alessandro Lasorsa, Vincenzo Aievola, et al.
Carcinogenesis|October 3, 2017
Kinome expression profiling of human neuroblastoma tumors identifies potential drug targets for ultra high-risk patientsRoberta Russo, Flora Cimmino, Lucia Pezone, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
American Journal of Hematology|March 7, 2023
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriersValeria Maria Pinto, Roberta Russo, Sabrina Quintino, et al.
Oncotarget|June 29, 2016
A comprehensive characterization of rare mitochondrial DNA variants in neuroblastomaFrancesco Maria Calabrese, Rosanna Clima, Piero Pignataro, et al.
Hemoglobin|December 13, 2019
A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek FamilyAlexandros Makis, Ioannis Georgiou, Jan Traeger-Synodinos, et al.
Nephron. Physiology|December 29, 2006
Characterization of two novel missense mutations in the AQP2 gene causing nephrogenic diabetes insipidusAchille Iolascon, Veruska Aglio, Grazia Tamma, et al.
Haematologica|August 1, 2009
A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesisAchille Iolascon, Luigia De Falco, Franck Borgese, et al.
Pageof 29