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Cancer Genetics
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April 15, 2014
Combinations of genetic data in a study of neuroblastoma risk genotypes
Mario Capasso, Francesco Maria Calabrese, Achille Iolascon, et al.
Genes
|
May 27, 2023
New Insights in 9q21.13 Microdeletion Syndrome: Genotype-Phenotype Correlation of 28 Patients
Alessandro De Falco, Achille Iolascon, Flora Ascione, et al.
International Journal of Nephrology
|
September 10, 2011
Molecular and genetic basis of inherited nephrotic syndrome
Maddalena Gigante, Matteo Piemontese, Loreto Gesualdo, et al.
Blood Cells, Molecules & Diseases
|
April 6, 2006
A novel R416C mutation in human DMT1 (SLC11A2) displays pleiotropic effects on function and causes microcytic anemia and hepatic iron overload
Steven Lam-Yuk-Tseung, Clara Camaschella, Achille Iolascon, et al.
European Journal of Internal Medicine
|
May 23, 2017
Clinical management of iron deficiency anemia in adults: Systemic review on advances in diagnosis and treatment
Lucia De Franceschi, Achille Iolascon, Ali Taher, et al.
European Journal of Internal Medicine
|
January 24, 2018
Microcytosis is important in screening of iron deficiency anemia
Lucia De Franceschi, Achille Iolascon, Ali Taher, et al.
Frontiers in Physiology
|
January 8, 2021
Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias
Roberta Russo, Roberta Marra, Barbara Eleni Rosato, et al.
Frontiers in Genetics
|
August 28, 2020
Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease <i>TMPRSS2</i> in Different Populations
Roberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, et al.
Frontiers in Oncology
|
December 31, 2020
A Targeted Gene Panel for Circulating Tumor DNA Sequencing in Neuroblastoma
Flora Cimmino, Vito Alessandro Lasorsa, Simona Vetrella, et al.
International Journal of Laboratory Hematology
|
May 15, 2024
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias
Roberta Russo, Achille Iolascon, Immacolata Andolfo, et al.
Page
of 29
Search research articles
Search
Showing results (31-40 of 290) with videos related to
Sort By:
Page
of 29
Cancer Genetics
|
April 15, 2014
Combinations of genetic data in a study of neuroblastoma risk genotypes
Mario Capasso, Francesco Maria Calabrese, Achille Iolascon, et al.
Genes
|
May 27, 2023
New Insights in 9q21.13 Microdeletion Syndrome: Genotype-Phenotype Correlation of 28 Patients
Alessandro De Falco, Achille Iolascon, Flora Ascione, et al.
International Journal of Nephrology
|
September 10, 2011
Molecular and genetic basis of inherited nephrotic syndrome
Maddalena Gigante, Matteo Piemontese, Loreto Gesualdo, et al.
Blood Cells, Molecules & Diseases
|
April 6, 2006
A novel R416C mutation in human DMT1 (SLC11A2) displays pleiotropic effects on function and causes microcytic anemia and hepatic iron overload
Steven Lam-Yuk-Tseung, Clara Camaschella, Achille Iolascon, et al.
European Journal of Internal Medicine
|
May 23, 2017
Clinical management of iron deficiency anemia in adults: Systemic review on advances in diagnosis and treatment
Lucia De Franceschi, Achille Iolascon, Ali Taher, et al.
European Journal of Internal Medicine
|
January 24, 2018
Microcytosis is important in screening of iron deficiency anemia
Lucia De Franceschi, Achille Iolascon, Ali Taher, et al.
Frontiers in Physiology
|
January 8, 2021
Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias
Roberta Russo, Roberta Marra, Barbara Eleni Rosato, et al.
Frontiers in Genetics
|
August 28, 2020
Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease <i>TMPRSS2</i> in Different Populations
Roberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, et al.
Frontiers in Oncology
|
December 31, 2020
A Targeted Gene Panel for Circulating Tumor DNA Sequencing in Neuroblastoma
Flora Cimmino, Vito Alessandro Lasorsa, Simona Vetrella, et al.
International Journal of Laboratory Hematology
|
May 15, 2024
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias
Roberta Russo, Achille Iolascon, Immacolata Andolfo, et al.
Page
of 29