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Luigia De Falco

Showing results (1-10 of 40) with videos related to

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Seminars in Hematology|September 30, 2009
Mutations in the gene encoding DMT1: clinical presentation and treatmentAchille Iolascon, Luigia De Falco
Haematologica|February 3, 2009
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesisAchille Iolascon, Luigia De Falco, Carole Beaumont
Seminars in Hematology|September 26, 2015
How I Diagnose Non-thalassemic Microcytic AnemiasMariasole Bruno, Luigia De Falco, Achille Iolascon
Pediatric Hematology and Oncology|April 28, 2016
Iron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutationsErtan Sal, Ebru Yılmaz Keskin, Idil Yenicesu, et al.
Haematologica|January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemiaMaria 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 modelRoberta Asci, Fara Vallefuoco, Immacolata Andolfo, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblingsMariateresa Falco, Annamaria Franzè, Sandra Iossa, et al.
Clinical Case Reports|October 19, 2019
Detection of SRY-positive46,XX male syndrome by the analysis of cell-free fetal DNA via non-invasive prenatal testingLuigia De Falco, Giovanni Savarese, Teresa Suero, et al.
The Turkish Journal of Pediatrics|January 3, 2014
Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?Ebru Yilmaz-Keskin, Ertan Sal, Luigia de Falco, et al.
Cells|July 12, 2024
Trisomy 21 with Maternally Inherited Balanced Translocation (15q;22q) in a Female Fetus: A Rare Case of Probable Interchromosomal EffectAlessandro De Falco, Antonella Gambale, Michele Pinelli, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Seminars in Hematology|September 30, 2009
Mutations in the gene encoding DMT1: clinical presentation and treatmentAchille Iolascon, Luigia De Falco
Haematologica|February 3, 2009
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesisAchille Iolascon, Luigia De Falco, Carole Beaumont
Seminars in Hematology|September 26, 2015
How I Diagnose Non-thalassemic Microcytic AnemiasMariasole Bruno, Luigia De Falco, Achille Iolascon
Pediatric Hematology and Oncology|April 28, 2016
Iron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutationsErtan Sal, Ebru Yılmaz Keskin, Idil Yenicesu, et al.
Haematologica|January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemiaMaria 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 modelRoberta Asci, Fara Vallefuoco, Immacolata Andolfo, et al.
American Journal of Medical Genetics. Part A|March 22, 2017
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblingsMariateresa Falco, Annamaria Franzè, Sandra Iossa, et al.
Clinical Case Reports|October 19, 2019
Detection of SRY-positive46,XX male syndrome by the analysis of cell-free fetal DNA via non-invasive prenatal testingLuigia De Falco, Giovanni Savarese, Teresa Suero, et al.
The Turkish Journal of Pediatrics|January 3, 2014
Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?Ebru Yilmaz-Keskin, Ertan Sal, Luigia de Falco, et al.
Cells|July 12, 2024
Trisomy 21 with Maternally Inherited Balanced Translocation (15q;22q) in a Female Fetus: A Rare Case of Probable Interchromosomal EffectAlessandro De Falco, Antonella Gambale, Michele Pinelli, et al.
Pageof 4