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Concetta Aloi

Showing results (11-20 of 18) with videos related to

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International Journal of Molecular Sciences|August 7, 2021
A Novel Genetic Variant in the WFS1 Gene in a Patient with Partial Uniparental Mero-Isodisomy of Chromosome 4Maurizio Delvecchio, Federica Ortolani, Orazio Palumbo, et al.
Plos One|January 13, 2012
Wolfram syndrome: new mutations, different phenotypeConcetta Aloi, Alessandro Salina, Lorenzo Pasquali, et al.
Biochemical and Biophysical Research Communications|August 12, 2009
Cell-cell bond modulates vascular smooth muscle cell responsiveness to Angiotensin IIChiara Barisione, Marzia Mura, Silvano Garibaldi, et al.
Plos One|December 29, 2010
p38 MAPK and JNK antagonistically control senescence and cytoplasmic p16INK4A expression in doxorubicin-treated endothelial progenitor cellsPaolo Spallarossa, Paola Altieri, Chiara Barisione, et al.
Life (Basel, Switzerland)|March 29, 2023
Automated Insulin Delivery (AID) Systems: Use and Efficacy in Children and Adults with Type 1 Diabetes and Other Forms of Diabetes in Europe in Early 2023Marta Bassi, Daniele Franzone, Francesca Dufour, et al.
Pediatric Research|July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlationsLuciana Rigoli, Concetta Aloi, Alessandro Salina, et al.
Frontiers in Medicine|June 9, 2025
Case Report: Beyond type 1 diabetes: a case of delayed MODY1 diagnosis and successful transition to sulfonylurea therapyChiara Gulisano, Concetta Aloi, Alessandro Salina, et al.
BMC Medical Genetics|July 25, 2014
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
International Journal of Molecular Sciences|August 7, 2021
A Novel Genetic Variant in the WFS1 Gene in a Patient with Partial Uniparental Mero-Isodisomy of Chromosome 4Maurizio Delvecchio, Federica Ortolani, Orazio Palumbo, et al.
Plos One|January 13, 2012
Wolfram syndrome: new mutations, different phenotypeConcetta Aloi, Alessandro Salina, Lorenzo Pasquali, et al.
Biochemical and Biophysical Research Communications|August 12, 2009
Cell-cell bond modulates vascular smooth muscle cell responsiveness to Angiotensin IIChiara Barisione, Marzia Mura, Silvano Garibaldi, et al.
Plos One|December 29, 2010
p38 MAPK and JNK antagonistically control senescence and cytoplasmic p16INK4A expression in doxorubicin-treated endothelial progenitor cellsPaolo Spallarossa, Paola Altieri, Chiara Barisione, et al.
Life (Basel, Switzerland)|March 29, 2023
Automated Insulin Delivery (AID) Systems: Use and Efficacy in Children and Adults with Type 1 Diabetes and Other Forms of Diabetes in Europe in Early 2023Marta Bassi, Daniele Franzone, Francesca Dufour, et al.
Pediatric Research|July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlationsLuciana Rigoli, Concetta Aloi, Alessandro Salina, et al.
Frontiers in Medicine|June 9, 2025
Case Report: Beyond type 1 diabetes: a case of delayed MODY1 diagnosis and successful transition to sulfonylurea therapyChiara Gulisano, Concetta Aloi, Alessandro Salina, et al.
BMC Medical Genetics|July 25, 2014
A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, et al.
Pageof 2