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European Journal of Haematology|September 25, 2014
Congenital erythropoietic porphyria linked to GATA1-R216W mutation: challenges for diagnosisElena Di Pierro, Roberta Russo, Zeynep Karakas, et al.
Frontiers in Physiology|April 2, 2019
PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood CellsImmacolata Andolfo, Gianluca De Rosa, Edoardo Errichiello, et al.
American Journal of Hematology|February 4, 2018
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemiasRoberta Russo, Immacolata Andolfo, Francesco Manna, et al.
Clinical Genetics|July 7, 2019
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predispositionAntonella Gambale, Roberta Russo, Immacolata Andolfo, et al.
Haematologica|May 7, 2016
Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemiaImmacolata Andolfo, Roberta Russo, Francesco Manna, et al.
Genes|July 2, 2021
Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 PatientsImmacolata Andolfo, Stefania Martone, Barbara Eleni Rosato, et al.
American Journal of Hematology|April 26, 2024
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patientsRoberta Marra, Antonella Nostroso, Barbara Eleni Rosato, et al.
Cancers|July 29, 2023
DICER1 Syndrome: A Multicenter Surgical Experience and Systematic ReviewClaudio Spinelli, Marco Ghionzoli, Linda Idrissi Sahli, 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.
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