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Alessandro De Luca

Showing results (21-30 of 192) with videos related to

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Annals of Human Genetics|June 2, 2021
External hydrocephalus as a prenatal feature of noonan syndromeGioia Mastromoro, Alessandro De Luca, Enrica Marchionni, et al.
Journal of Neurogenetics|November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomyFrancesco Nicita, Giacomo Garone, Laura Papetti, et al.
Annali Italiani Di Chirurgia|September 19, 2023
Neither inguinoscrotal hernia nor hydrocele misunderstood giant testicular neoplasm. Case report and literature reviewAlessandro De Luca, Lucia Franzoso, Viviana Danese, et al.
Sensors (Basel, Switzerland)|August 26, 2022
Lamb Wave Detection for Structural Health Monitoring Using a ϕ-OTDR SystemRizwan Zahoor, Enis Cerri, Raffaele Vallifuoco, et al.
Indian Journal of Pediatrics|June 20, 2020
Neonatal Marfan Syndrome by Inherited MutationGioia Mastromoro, Valentina Guida, Raffaella Cellitti, et al.
JPRAS Open|December 18, 2023
Evaluating the Quality of Online Patient Information for Prepectoral Breast Reconstruction Using Polyurethane-Coated Breast ImplantsEdoardo Bruno, Gianluca Borea, Roberto Valeriani, et al.
Archives of Pathology & Laboratory Medicine|April 7, 2011
Immunohistochemical expression of neurotrophic tyrosine kinase receptors 1 and 2 in lung carcinoma: potential discriminators between squamous and nonsquamous subtypesJefferson Terry, Alessandro De Luca, Samuel Leung, et al.
Human Mutation|February 22, 2002
Reliability of DHPLC in mutational screening of beta-globin (HBB) allelesAlessia Colosimo, Valentina Guida, Alessandro De Luca, et al.
Cancer Cell International|January 27, 2018
A possible role for selenoprotein glutathione peroxidase (GPx1) and thioredoxin reductases (TrxR1) in thyroid cancer: our experience in thyroid surgeryAlessio Metere, Francesca Frezzotti, Claire Elizabeth Graves, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Germline mosaicism in neurofibromatosis type 1 due to a paternally derived multi-exon deletionIrene Bottillo, Isabella Torrente, Valentina Lanari, et al.
Pageof 20

Showing results (21-30 of 192) with videos related to

Sort By:
Pageof 20
Annals of Human Genetics|June 2, 2021
External hydrocephalus as a prenatal feature of noonan syndromeGioia Mastromoro, Alessandro De Luca, Enrica Marchionni, et al.
Journal of Neurogenetics|November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomyFrancesco Nicita, Giacomo Garone, Laura Papetti, et al.
Annali Italiani Di Chirurgia|September 19, 2023
Neither inguinoscrotal hernia nor hydrocele misunderstood giant testicular neoplasm. Case report and literature reviewAlessandro De Luca, Lucia Franzoso, Viviana Danese, et al.
Sensors (Basel, Switzerland)|August 26, 2022
Lamb Wave Detection for Structural Health Monitoring Using a ϕ-OTDR SystemRizwan Zahoor, Enis Cerri, Raffaele Vallifuoco, et al.
Indian Journal of Pediatrics|June 20, 2020
Neonatal Marfan Syndrome by Inherited MutationGioia Mastromoro, Valentina Guida, Raffaella Cellitti, et al.
JPRAS Open|December 18, 2023
Evaluating the Quality of Online Patient Information for Prepectoral Breast Reconstruction Using Polyurethane-Coated Breast ImplantsEdoardo Bruno, Gianluca Borea, Roberto Valeriani, et al.
Archives of Pathology & Laboratory Medicine|April 7, 2011
Immunohistochemical expression of neurotrophic tyrosine kinase receptors 1 and 2 in lung carcinoma: potential discriminators between squamous and nonsquamous subtypesJefferson Terry, Alessandro De Luca, Samuel Leung, et al.
Human Mutation|February 22, 2002
Reliability of DHPLC in mutational screening of beta-globin (HBB) allelesAlessia Colosimo, Valentina Guida, Alessandro De Luca, et al.
Cancer Cell International|January 27, 2018
A possible role for selenoprotein glutathione peroxidase (GPx1) and thioredoxin reductases (TrxR1) in thyroid cancer: our experience in thyroid surgeryAlessio Metere, Francesca Frezzotti, Claire Elizabeth Graves, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Germline mosaicism in neurofibromatosis type 1 due to a paternally derived multi-exon deletionIrene Bottillo, Isabella Torrente, Valentina Lanari, et al.
Pageof 20