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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 2012
Maurizio Delvecchio, Enza Mozzillo, Giuseppina Salzano, et al.
American Journal of Human Genetics
|
June 16, 2015
Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus
Sabrina Prudente, Prapaporn Jungtrakoon, Antonella Marucci, et al.
The Lancet. Diabetes & Endocrinology
|
June 9, 2018
Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
Pamela Bowman, Åsta Sulen, Fabrizio Barbetti, et al.
Acta Diabetologica
|
June 28, 2018
Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing?
Maurizio Delvecchio, Giuseppina Salzano, Clara Bonura, et al.
The Journal of Biological Chemistry
|
January 29, 2005
Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young
Anna L Gloyn, Stella Odili, Dorothy Zelent, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2024
The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022
Novella Rapini, Maurizio Delvecchio, Mafalda Mucciolo, et al.
European Journal of Endocrinology
|
February 19, 2021
Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy
Riccardo Bonfanti, Dario Iafusco, Ivana Rabbone, et al.
Acta Diabetologica
|
May 18, 2026
Screening practices for diabetic peripheral neuropathy in pediatric type 1 diabetes: a nationwide survey by the ISPED Diabetes Study Group
Bruno Bombaci, Marta Bassi, Valeria Castorani, et al.
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Showing results (81-90 of 88) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 88 results.
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 2012
Maurizio Delvecchio, Enza Mozzillo, Giuseppina Salzano, et al.
American Journal of Human Genetics
|
June 16, 2015
Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus
Sabrina Prudente, Prapaporn Jungtrakoon, Antonella Marucci, et al.
The Lancet. Diabetes & Endocrinology
|
June 9, 2018
Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
Pamela Bowman, Åsta Sulen, Fabrizio Barbetti, et al.
Acta Diabetologica
|
June 28, 2018
Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing?
Maurizio Delvecchio, Giuseppina Salzano, Clara Bonura, et al.
The Journal of Biological Chemistry
|
January 29, 2005
Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young
Anna L Gloyn, Stella Odili, Dorothy Zelent, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2024
The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022
Novella Rapini, Maurizio Delvecchio, Mafalda Mucciolo, et al.
European Journal of Endocrinology
|
February 19, 2021
Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy
Riccardo Bonfanti, Dario Iafusco, Ivana Rabbone, et al.
Acta Diabetologica
|
May 18, 2026
Screening practices for diabetic peripheral neuropathy in pediatric type 1 diabetes: a nationwide survey by the ISPED Diabetes Study Group
Bruno Bombaci, Marta Bassi, Valeria Castorani, et al.
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of 9