Search research articles
Contact Us
Filters
Showing results (11-20 of 18) with videos related to
Page
of 2
Sort By:
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 4
Maurizio Delvecchio, Federica Ortolani, Orazio Palumbo, et al.
Plos One
|
January 13, 2012
Wolfram syndrome: new mutations, different phenotype
Concetta 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 II
Chiara 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 cells
Paolo 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 2023
Marta Bassi, Daniele Franzone, Francesca Dufour, et al.
Pediatric Research
|
July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations
Luciana 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 therapy
Chiara 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 2
Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 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 4
Maurizio Delvecchio, Federica Ortolani, Orazio Palumbo, et al.
Plos One
|
January 13, 2012
Wolfram syndrome: new mutations, different phenotype
Concetta 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 II
Chiara 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 cells
Paolo 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 2023
Marta Bassi, Daniele Franzone, Francesca Dufour, et al.
Pediatric Research
|
July 3, 2019
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations
Luciana 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 therapy
Chiara 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 2
Enza Mozzillo, Maurizio Delvecchio, Massimo Carella, et al.
Page
of 2