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Italian Journal of Pediatrics
|
May 12, 2026
A new 308 A-G substitution in HBG2 in an acyanotic newborn: case report
Stefano Pellicani, Manuela Capozza, Immacolata Andolfo, 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 scores
Roberta Russo, Antonella Gambale, Concetta Langella, et al.
Hemoglobin
|
November 27, 2024
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect
Georgios Dryllis, Roberta Russo, Immacolata Andolfo, et al.
Neuroscience Research
|
September 24, 2013
Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model
Roberta Asci, Fara Vallefuoco, Immacolata Andolfo, et al.
Scientific Reports
|
June 10, 2015
Inhibition of hypoxia inducible factors combined with all-trans retinoic acid treatment enhances glial transdifferentiation of neuroblastoma cells
Flora Cimmino, Lucia Pezone, Marianna Avitabile, et al.
Italian Journal of Pediatrics
|
July 25, 2020
A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature
Daniele Zama, Giulia Giulietti, Edoardo Muratore, et al.
Genes
|
September 28, 2024
A Novel De Novo <i>STAG1</i> Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity
Lorenzo Cipriano, Roberta Russo, Immacolata Andolfo, et al.
American Journal of Hematology
|
September 7, 2018
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients
Immacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, et al.
Expert Opinion on Biological Therapy
|
April 2, 2021
Recommendations for pregnancy in Fanconi anemia
Charbel F Matar, Rayan Bou-Fakhredin, Roberta Russo, et al.
Journal of Cellular and Molecular Medicine
|
April 27, 2020
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma
Immacolata Andolfo, Vito A Lasorsa, Francesco Manna, et al.
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Search research articles
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Showing results (11-20 of 92) with videos related to
Sort By:
Page
of 10
Italian Journal of Pediatrics
|
May 12, 2026
A new 308 A-G substitution in HBG2 in an acyanotic newborn: case report
Stefano Pellicani, Manuela Capozza, Immacolata Andolfo, 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 scores
Roberta Russo, Antonella Gambale, Concetta Langella, et al.
Hemoglobin
|
November 27, 2024
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect
Georgios Dryllis, Roberta Russo, Immacolata Andolfo, et al.
Neuroscience Research
|
September 24, 2013
Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model
Roberta Asci, Fara Vallefuoco, Immacolata Andolfo, et al.
Scientific Reports
|
June 10, 2015
Inhibition of hypoxia inducible factors combined with all-trans retinoic acid treatment enhances glial transdifferentiation of neuroblastoma cells
Flora Cimmino, Lucia Pezone, Marianna Avitabile, et al.
Italian Journal of Pediatrics
|
July 25, 2020
A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature
Daniele Zama, Giulia Giulietti, Edoardo Muratore, et al.
Genes
|
September 28, 2024
A Novel De Novo <i>STAG1</i> Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical Heterogeneity
Lorenzo Cipriano, Roberta Russo, Immacolata Andolfo, et al.
American Journal of Hematology
|
September 7, 2018
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients
Immacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, et al.
Expert Opinion on Biological Therapy
|
April 2, 2021
Recommendations for pregnancy in Fanconi anemia
Charbel F Matar, Rayan Bou-Fakhredin, Roberta Russo, et al.
Journal of Cellular and Molecular Medicine
|
April 27, 2020
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma
Immacolata Andolfo, Vito A Lasorsa, Francesco Manna, et al.
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of 10