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Alessandro Mauro Spinelli

Showing results (1-10 of 16) with videos related to

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Nutrients|July 20, 2018
Nutrition and Lung GrowthMichele Arigliani, Alessandro Mauro Spinelli, Ilaria Liguoro, et al.
Transplantation|November 26, 2019
The Authors' Reply: The tRNA(Ile) Variant m.4309G>A May Not Cause Kearns-Sayre SyndromeConcetta Di Nora, Alessandro Mauro Spinelli, Maurizio Scarpa, et al.
Italian Journal of Pediatrics|July 12, 2019
Unilateral testicular enlargement in a teenager with Beckwith-Wiedemann syndrome: a case reportMaria Chiara Pellegrin, Alessandro Mauro Spinelli, Gianluca Tornese, et al.
Immunology Letters|April 17, 2020
Corrigendum to "Tregs and Th17 lymphocytes in human DYRK1A haploinsufficiency" [Immunol. Lett. 214 (2019) 52-54]Erica Valencic, Elisa Piscianz, Fabio Sirchia, et al.
Immunology Letters|August 24, 2019
Tregs and Th17 lymphocytes in human DYRK1A haploinsufficiencyErica Valencic, Elisa Piscianz, Fabio Sirchia, et al.
American Journal of Medical Genetics. Part A|April 16, 2017
Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literatureLaura Travan, Samuele Naviglio, Angela De Cunto, et al.
Molecular Genetics & Genomic Medicine|January 11, 2019
Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysisRoberta Bottega, Stefania Cappellani, Antonella Fabretto, et al.
American Journal of Medical Genetics. Part A|June 26, 2024
Joint contractures is a recurrent clinical feature of individuals with neurodevelopmental disorder due to FOXP1 likely gene disruptive variantsCristina Peduto, Gerarda Cappuccio, Roberta Zeuli, et al.
American Journal of Medical Genetics. Part A|January 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defectsGerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, et al.
International Journal of Cancer|January 8, 2019
Insight into genetic susceptibility to male breast cancer by multigene panel testing: Results from a multicenter study in ItalyPiera Rizzolo, Veronica Zelli, Valentina Silvestri, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Nutrients|July 20, 2018
Nutrition and Lung GrowthMichele Arigliani, Alessandro Mauro Spinelli, Ilaria Liguoro, et al.
Transplantation|November 26, 2019
The Authors' Reply: The tRNA(Ile) Variant m.4309G>A May Not Cause Kearns-Sayre SyndromeConcetta Di Nora, Alessandro Mauro Spinelli, Maurizio Scarpa, et al.
Italian Journal of Pediatrics|July 12, 2019
Unilateral testicular enlargement in a teenager with Beckwith-Wiedemann syndrome: a case reportMaria Chiara Pellegrin, Alessandro Mauro Spinelli, Gianluca Tornese, et al.
Immunology Letters|April 17, 2020
Corrigendum to "Tregs and Th17 lymphocytes in human DYRK1A haploinsufficiency" [Immunol. Lett. 214 (2019) 52-54]Erica Valencic, Elisa Piscianz, Fabio Sirchia, et al.
Immunology Letters|August 24, 2019
Tregs and Th17 lymphocytes in human DYRK1A haploinsufficiencyErica Valencic, Elisa Piscianz, Fabio Sirchia, et al.
American Journal of Medical Genetics. Part A|April 16, 2017
Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literatureLaura Travan, Samuele Naviglio, Angela De Cunto, et al.
Molecular Genetics & Genomic Medicine|January 11, 2019
Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysisRoberta Bottega, Stefania Cappellani, Antonella Fabretto, et al.
American Journal of Medical Genetics. Part A|June 26, 2024
Joint contractures is a recurrent clinical feature of individuals with neurodevelopmental disorder due to FOXP1 likely gene disruptive variantsCristina Peduto, Gerarda Cappuccio, Roberta Zeuli, et al.
American Journal of Medical Genetics. Part A|January 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defectsGerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, et al.
International Journal of Cancer|January 8, 2019
Insight into genetic susceptibility to male breast cancer by multigene panel testing: Results from a multicenter study in ItalyPiera Rizzolo, Veronica Zelli, Valentina Silvestri, et al.
Pageof 2