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Alessandro De Luca

Showing results (11-20 of 192) with videos related to

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Diagnostics (Basel, Switzerland)|February 26, 2025
Fetal Hydrops: Genetic Dissection of an Unspecific Sonographic Finding-A Comprehensive ReviewGioia Mastromoro, Daniele Guadagnolo, Alessandro De Luca, et al.
American Journal of Medical Genetics. Part A|March 13, 2020
Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from IranHossein Hozhabri, Mehrdad Talebi, Mohammad Y V Mehrjardi, et al.
Surgical Technology International|June 10, 2015
Mid-Term Follow Up of TAPP Hernia Repair Without Staples and Glue: An Audit of the DataGiuseppe Piccinni, Giuseppe Massimiliano De Luca, Alessandro De Luca, et al.
Acta Neurologica Belgica|January 11, 2023
Cervical dystonia following brain tumor: description of an unreported case and a systematic review of literatureAssunta Trinchillo, Maria Cecilia D'Asdia, Alessandro De Luca, et al.
Archives of Orthopaedic and Trauma Surgery|July 5, 2022
Should the early surgery threshold be moved to 72 h in over-85 patients with hip fracture? A single-center retrospective evaluation on 941 patientsAlessandro De Luca, Luigi Murena, Michela Zanetti, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquid chromatography (DHPLC)Elisabetta Flex, Alessandro De Luca, Maria Rosaria D'Apice, et al.
Journal of Clinical Medicine|November 25, 2023
Novel Genetic Microvascular Dysplasia Causing Hypoperfusion of Cardiac, Renal, and Cerebral CirculationAndrea Frustaci, Rosario Cianci, Romina Verardo, et al.
Sensors (Basel, Switzerland)|November 27, 2025
Domain-Adaptive Graph Attention Semi-Supervised Network for Temperature-Resilient SHM of Composite PlatesNima Rezazadeh, Alessandro De Luca, Donato Perfetto, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2015
Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 geneGemma Tumminelli, Ilaria Di Donato, Valentina Guida, et al.
Parkinsonism & Related Disorders|April 28, 2023
A novel ANO3 variant in two siblings with different phenotypesMarcello Esposito, Assunta Trinchillo, Francesca Piceci-Sparascio, et al.
Pageof 20

Showing results (11-20 of 192) with videos related to

Sort By:
Pageof 20
Diagnostics (Basel, Switzerland)|February 26, 2025
Fetal Hydrops: Genetic Dissection of an Unspecific Sonographic Finding-A Comprehensive ReviewGioia Mastromoro, Daniele Guadagnolo, Alessandro De Luca, et al.
American Journal of Medical Genetics. Part A|March 13, 2020
Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from IranHossein Hozhabri, Mehrdad Talebi, Mohammad Y V Mehrjardi, et al.
Surgical Technology International|June 10, 2015
Mid-Term Follow Up of TAPP Hernia Repair Without Staples and Glue: An Audit of the DataGiuseppe Piccinni, Giuseppe Massimiliano De Luca, Alessandro De Luca, et al.
Acta Neurologica Belgica|January 11, 2023
Cervical dystonia following brain tumor: description of an unreported case and a systematic review of literatureAssunta Trinchillo, Maria Cecilia D'Asdia, Alessandro De Luca, et al.
Archives of Orthopaedic and Trauma Surgery|July 5, 2022
Should the early surgery threshold be moved to 72 h in over-85 patients with hip fracture? A single-center retrospective evaluation on 941 patientsAlessandro De Luca, Luigi Murena, Michela Zanetti, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquid chromatography (DHPLC)Elisabetta Flex, Alessandro De Luca, Maria Rosaria D'Apice, et al.
Journal of Clinical Medicine|November 25, 2023
Novel Genetic Microvascular Dysplasia Causing Hypoperfusion of Cardiac, Renal, and Cerebral CirculationAndrea Frustaci, Rosario Cianci, Romina Verardo, et al.
Sensors (Basel, Switzerland)|November 27, 2025
Domain-Adaptive Graph Attention Semi-Supervised Network for Temperature-Resilient SHM of Composite PlatesNima Rezazadeh, Alessandro De Luca, Donato Perfetto, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2015
Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 geneGemma Tumminelli, Ilaria Di Donato, Valentina Guida, et al.
Parkinsonism & Related Disorders|April 28, 2023
A novel ANO3 variant in two siblings with different phenotypesMarcello Esposito, Assunta Trinchillo, Francesca Piceci-Sparascio, et al.
Pageof 20