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Alessandro De Luca

Showing results (71-80 of 192) with videos related to

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Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
Genetic Testing|March 21, 2006
Combinatorial sequencing-by-hybridization: analysis of the NF1 geneAnnalisa Schirinzi, Snezana Drmanac, Bruno Dallapiccola, et al.
Lipids in Health and Disease|November 30, 2024
Assessment of plasma resolvin levels in women with breast cancer and their associations with disease presentation and immunohistochemical characteristicsAlessio Molfino, Giovanni Imbimbo, Gerardo Salerno, et al.
BMC Medical Genetics|February 14, 2007
Functional analysis of splicing mutations in exon 7 of NF1 geneIrene Bottillo, Alessandro De Luca, Annalisa Schirinzi, et al.
BMC Medical Genomics|March 26, 2021
Prenatal findings of cataract and arthrogryposis: recurrence of cerebro-oculo-facio-skeletal syndrome and review of differential diagnosisFabio Sirchia, Ilaria Fantasia, Agnese Feresin, et al.
Human Mutation|November 9, 2004
Mutations of the Nogo-66 receptor (RTN4R) gene in schizophreniaLorenzo Sinibaldi, Alessandro De Luca, Emanuele Bellacchio, et al.
Human Molecular Genetics|December 10, 2009
Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activationLothar Gremer, Alessandro De Luca, Torsten Merbitz-Zahradnik, et al.
Journal of the American Heart Association|February 15, 2018
Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic CorrelationAndrea Frustaci, Alessandro De Luca, Valentina Guida, et al.
International Journal of Surgery Case Reports|May 22, 2018
Congenital diaphragmatic disease: An unusual presentation in adulthood. Case reportAngela Gurrado, Roberta Maria Isernia, Alessandro De Luca, et al.
Pageof 20

Showing results (71-80 of 192) with videos related to

Sort By:
Pageof 20
Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
Genetic Testing|March 21, 2006
Combinatorial sequencing-by-hybridization: analysis of the NF1 geneAnnalisa Schirinzi, Snezana Drmanac, Bruno Dallapiccola, et al.
Lipids in Health and Disease|November 30, 2024
Assessment of plasma resolvin levels in women with breast cancer and their associations with disease presentation and immunohistochemical characteristicsAlessio Molfino, Giovanni Imbimbo, Gerardo Salerno, et al.
BMC Medical Genetics|February 14, 2007
Functional analysis of splicing mutations in exon 7 of NF1 geneIrene Bottillo, Alessandro De Luca, Annalisa Schirinzi, et al.
BMC Medical Genomics|March 26, 2021
Prenatal findings of cataract and arthrogryposis: recurrence of cerebro-oculo-facio-skeletal syndrome and review of differential diagnosisFabio Sirchia, Ilaria Fantasia, Agnese Feresin, et al.
Human Mutation|November 9, 2004
Mutations of the Nogo-66 receptor (RTN4R) gene in schizophreniaLorenzo Sinibaldi, Alessandro De Luca, Emanuele Bellacchio, et al.
Human Molecular Genetics|December 10, 2009
Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activationLothar Gremer, Alessandro De Luca, Torsten Merbitz-Zahradnik, et al.
Journal of the American Heart Association|February 15, 2018
Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic CorrelationAndrea Frustaci, Alessandro De Luca, Valentina Guida, et al.
International Journal of Surgery Case Reports|May 22, 2018
Congenital diaphragmatic disease: An unusual presentation in adulthood. Case reportAngela Gurrado, Roberta Maria Isernia, Alessandro De Luca, et al.
Pageof 20