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Achille Iolascon

Showing results (41-50 of 290) with videos related to

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Clinics in Perinatology|June 9, 2004
The role of molecular genetics in the pathogenesis and diagnosis of neonatal sepsisAntonio Del Vecchio, Nicola Laforgia, Mario Capasso, et al.
Genes & Diseases|September 29, 2025
CTpredX: Enhancing missense variant pathogenicity prediction in childhood cancer predisposition genesFerdinando Bonfiglio, Vito Alessandro Lasorsa, Giampiero Pirozzi, et al.
Carcinogenesis|March 16, 2006
Plakoglobin is differentially expressed in alveolar and embryonal rhabdomyosarcoma and is regulated by DNA methylation and histone acetylationTamara Gastaldi, Paolo Bonvini, Francesca Sartori, et al.
Journal of Pediatric Hematology/Oncology|October 9, 2019
Hematopoietic Stem Cell Transplantation in Congenital Dyserythropetic Anemia Type II: A Case Report and Review of the LiteratureVedat Uygun, Roberta Russo, Gülsün Karasu, et al.
American Journal of Hematology|July 22, 2014
Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scoresRoberta Russo, Antonella Gambale, Concetta Langella, et al.
Molecular Genetics & Genomic Medicine|December 19, 2020
RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanismEdoardo Errichiello, Roberto Giorda, Antonella Gambale, et al.
Expert Opinion on Investigational Drugs|December 19, 2019
Emerging drugs in randomized controlled trials for sickle cell disease: are we on the brink of a new era in research and treatment?Alessandro Matte, Maria Domenica Cappellini, Achille Iolascon, et al.
Blood|September 15, 2005
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)Achille Iolascon, Maria d'Apolito, Veronica Servedio, et al.
Frontiers in Oncology|November 16, 2020
Genetic Predisposition to Solid Pediatric CancersMario Capasso, Annalaura Montella, Matilde Tirelli, et al.
Exploration of Targeted Anti-Tumor Therapy|May 15, 2024
Improving single nucleotide polymorphisms genotyping accuracy for dihydropyrimidine dehydrogenase testing in pharmacogeneticsAnnalaura Montella, Sueva Cantalupo, Giuseppe D'Alterio, et al.
Pageof 29

Showing results (41-50 of 290) with videos related to

Sort By:
Pageof 29
Clinics in Perinatology|June 9, 2004
The role of molecular genetics in the pathogenesis and diagnosis of neonatal sepsisAntonio Del Vecchio, Nicola Laforgia, Mario Capasso, et al.
Genes & Diseases|September 29, 2025
CTpredX: Enhancing missense variant pathogenicity prediction in childhood cancer predisposition genesFerdinando Bonfiglio, Vito Alessandro Lasorsa, Giampiero Pirozzi, et al.
Carcinogenesis|March 16, 2006
Plakoglobin is differentially expressed in alveolar and embryonal rhabdomyosarcoma and is regulated by DNA methylation and histone acetylationTamara Gastaldi, Paolo Bonvini, Francesca Sartori, et al.
Journal of Pediatric Hematology/Oncology|October 9, 2019
Hematopoietic Stem Cell Transplantation in Congenital Dyserythropetic Anemia Type II: A Case Report and Review of the LiteratureVedat Uygun, Roberta Russo, Gülsün Karasu, et al.
American Journal of Hematology|July 22, 2014
Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scoresRoberta Russo, Antonella Gambale, Concetta Langella, et al.
Molecular Genetics & Genomic Medicine|December 19, 2020
RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanismEdoardo Errichiello, Roberto Giorda, Antonella Gambale, et al.
Expert Opinion on Investigational Drugs|December 19, 2019
Emerging drugs in randomized controlled trials for sickle cell disease: are we on the brink of a new era in research and treatment?Alessandro Matte, Maria Domenica Cappellini, Achille Iolascon, et al.
Blood|September 15, 2005
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)Achille Iolascon, Maria d'Apolito, Veronica Servedio, et al.
Frontiers in Oncology|November 16, 2020
Genetic Predisposition to Solid Pediatric CancersMario Capasso, Annalaura Montella, Matilde Tirelli, et al.
Exploration of Targeted Anti-Tumor Therapy|May 15, 2024
Improving single nucleotide polymorphisms genotyping accuracy for dihydropyrimidine dehydrogenase testing in pharmacogeneticsAnnalaura Montella, Sueva Cantalupo, Giuseppe D'Alterio, et al.
Pageof 29