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Alessandro Salina

Showing results (11-20 of 16) with videos related to

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Pediatric Research|July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlationsLuciana Rigoli, Concetta Aloi, Alessandro Salina, 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.
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.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012Maurizio Delvecchio, Enza Mozzillo, Giuseppina Salzano, et al.
International Journal of Neonatal Screening|August 23, 2022
Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National ExperienceMargherita Ruoppolo, Sabrina Malvagia, Sara Boenzi, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Pediatric Research|July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlationsLuciana Rigoli, Concetta Aloi, Alessandro Salina, 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.
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.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012Maurizio Delvecchio, Enza Mozzillo, Giuseppina Salzano, et al.
International Journal of Neonatal Screening|August 23, 2022
Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National ExperienceMargherita Ruoppolo, Sabrina Malvagia, Sara Boenzi, et al.
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