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Pediatric Annals
|
June 12, 2008
Red cell membrane disorders in pediatrics
Achille Iolascon, Carmelo Piscopo, Loredana Boschetto
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.
Children (Basel, Switzerland)
|
May 25, 2024
Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel Mutation
Lorenzo Cipriano, Raffaele Piscopo, Chiara Aiello, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
March 23, 2013
Pediatric portal vein thrombosis: more on thrombophilic risk factors
Pietro Vajro, Riccardo Campanile, Maria Caropreso, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
September 3, 2010
Genetic prothrombotic risk factors in children with extrahepatic portal vein obstruction
Maria Caropreso, Riccardo Campanile, Sergio Maddaluno, 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.
Clinical Endocrinology
|
May 22, 2025
Efficacy and Safety of Three-Years Growth Hormone Treatment in Girls With Turner Syndrome and Growth Hormone Deficiency: A Case-Control Study
Rosario Ferrigno, Daniela Cioffi, Valeria Pellino, et al.
Pediatric Research
|
February 23, 2007
Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome
Mario Capasso, Rosa Anna Avvisati, Carmelo Piscopo, et al.
American Journal of Hematology
|
January 8, 2010
Identification and molecular characterization of the --CAMPANIA deletion, a novel alpha (0) -thalassemic defect, in two unrelated Italian families [corrected]
Raffaele Sessa, Stella Puzone, Massimiliano Ammirabile, et al.
Blood Transfusion = Trasfusione Del Sangue
|
January 22, 2011
Congenital dyserythropoietic anaemias: new acquisitions
Achille Iolascon, Roberta Russo, Maria Rosaria Esposito, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Pediatric Annals
|
June 12, 2008
Red cell membrane disorders in pediatrics
Achille Iolascon, Carmelo Piscopo, Loredana Boschetto
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.
Children (Basel, Switzerland)
|
May 25, 2024
Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel Mutation
Lorenzo Cipriano, Raffaele Piscopo, Chiara Aiello, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
March 23, 2013
Pediatric portal vein thrombosis: more on thrombophilic risk factors
Pietro Vajro, Riccardo Campanile, Maria Caropreso, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
September 3, 2010
Genetic prothrombotic risk factors in children with extrahepatic portal vein obstruction
Maria Caropreso, Riccardo Campanile, Sergio Maddaluno, 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.
Clinical Endocrinology
|
May 22, 2025
Efficacy and Safety of Three-Years Growth Hormone Treatment in Girls With Turner Syndrome and Growth Hormone Deficiency: A Case-Control Study
Rosario Ferrigno, Daniela Cioffi, Valeria Pellino, et al.
Pediatric Research
|
February 23, 2007
Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome
Mario Capasso, Rosa Anna Avvisati, Carmelo Piscopo, et al.
American Journal of Hematology
|
January 8, 2010
Identification and molecular characterization of the --CAMPANIA deletion, a novel alpha (0) -thalassemic defect, in two unrelated Italian families [corrected]
Raffaele Sessa, Stella Puzone, Massimiliano Ammirabile, et al.
Blood Transfusion = Trasfusione Del Sangue
|
January 22, 2011
Congenital dyserythropoietic anaemias: new acquisitions
Achille Iolascon, Roberta Russo, Maria Rosaria Esposito, et al.
Page
of 5