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Children (Basel, Switzerland)
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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.
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.
Journal of Perinatal Medicine
|
May 16, 2002
Neonatal hyperbilirubinemia and Gilbert's syndrome
Nicola Laforgia, Maria Felicia Faienza, Andrea Rinaldi, 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.
Haematologica
|
January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia
Maria D'Apolito, Agnese Marrone, Veronica Servedio, 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.
Cancer Genetics and Cytogenetics
|
June 20, 2002
Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors
Lucia Giordani, Achille Iolascon, Veronica Servedio, et al.
Journal of Cancer Research and Clinical Oncology
|
June 27, 2009
A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma in Southern Italian population
Mario Capasso, Fabrizio Ayala, Roberta Russo, et al.
Biology of the Neonate
|
June 1, 2006
Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism
Alberto Berardi, Licia Lugli, Fabrizio Ferrari, et al.
Journal of Proteome Research
|
May 24, 2008
Changes of the hepatic proteome in hepatitis B-infected mouse model at early stages of fibrosis
Daniela Spano, Flora Cimmino, Mario Capasso, et al.
Page
of 29
Search research articles
Search
Showing results (51-60 of 290) with videos related to
Sort By:
Page
of 29
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.
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.
Journal of Perinatal Medicine
|
May 16, 2002
Neonatal hyperbilirubinemia and Gilbert's syndrome
Nicola Laforgia, Maria Felicia Faienza, Andrea Rinaldi, 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.
Haematologica
|
January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia
Maria D'Apolito, Agnese Marrone, Veronica Servedio, 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.
Cancer Genetics and Cytogenetics
|
June 20, 2002
Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors
Lucia Giordani, Achille Iolascon, Veronica Servedio, et al.
Journal of Cancer Research and Clinical Oncology
|
June 27, 2009
A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma in Southern Italian population
Mario Capasso, Fabrizio Ayala, Roberta Russo, et al.
Biology of the Neonate
|
June 1, 2006
Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism
Alberto Berardi, Licia Lugli, Fabrizio Ferrari, et al.
Journal of Proteome Research
|
May 24, 2008
Changes of the hepatic proteome in hepatitis B-infected mouse model at early stages of fibrosis
Daniela Spano, Flora Cimmino, Mario Capasso, et al.
Page
of 29