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Diabetes
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January 30, 2007
An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of developmental delay, epilepsy, and neonatal diabetes
Ricard Masia, Joseph C Koster, Stefano Tumini, et al.
International Journal of Environmental Research and Public Health
|
December 30, 2025
Effect of Atmospheric Temperature Variations on Glycemic Patterns of Patients with Type 1 Diabetes: Analysis as a Function of Different Therapeutic Treatments
Alessandra Mascitelli, Stefano Tumini, Piero Chiacchiaretta, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
August 11, 2020
Diabetic ketoacidosis: A consensus statement of the Italian Association of Medical Diabetologists (AMD), Italian Society of Diabetology (SID), Italian Society of Endocrinology and Pediatric Diabetoloy (SIEDP)
Annunziata Lapolla, Flavia Amaro, Daniela Bruttomesso, et al.
Diabetes Care
|
February 11, 2012
Infant and toddler type 1 diabetes: complications after 20 years' duration
Silvana Salardi, Massimo Porta, Giulio Maltoni, et al.
Asian Journal of Andrology
|
December 22, 2007
Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome
Florina Raicu, Rossella Giuliani, Valentina Gatta, et al.
Diabetes Technology & Therapeutics
|
November 13, 2009
Insulin pump therapy management in very young children with type 1 diabetes using continuous subcutaneous insulin infusion
Ivana Rabbone, Andrea Scaramuzza, Adriana Bobbio, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2012
A case of congenital hypothyroidism in PHACE syndrome
Silvia Carinci, Stefano Tumini, Nicola Pietro Consilvio, et al.
Journal of Human Genetics
|
November 9, 2006
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay
Valentina Gatta, Ivana Antonucci, Elisena Morizio, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 16, 2010
Genital sanguineous discharge in prepuberty: a case of mullerian papilloma of vagina in a nine-year-old girl
Stefano Tumini, Silvia Carinci, Maria Teresa Anzellotti, et al.
Diabetes Research and Clinical Practice
|
January 20, 2009
Novel mutations in GCK and HNF1A genes in Italian families with MODY phenotype
Alessia Cappelli, Stefano Tumini, Agostino Consoli, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
Diabetes
|
January 30, 2007
An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of developmental delay, epilepsy, and neonatal diabetes
Ricard Masia, Joseph C Koster, Stefano Tumini, et al.
International Journal of Environmental Research and Public Health
|
December 30, 2025
Effect of Atmospheric Temperature Variations on Glycemic Patterns of Patients with Type 1 Diabetes: Analysis as a Function of Different Therapeutic Treatments
Alessandra Mascitelli, Stefano Tumini, Piero Chiacchiaretta, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
August 11, 2020
Diabetic ketoacidosis: A consensus statement of the Italian Association of Medical Diabetologists (AMD), Italian Society of Diabetology (SID), Italian Society of Endocrinology and Pediatric Diabetoloy (SIEDP)
Annunziata Lapolla, Flavia Amaro, Daniela Bruttomesso, et al.
Diabetes Care
|
February 11, 2012
Infant and toddler type 1 diabetes: complications after 20 years' duration
Silvana Salardi, Massimo Porta, Giulio Maltoni, et al.
Asian Journal of Andrology
|
December 22, 2007
Novel mutation in the ligand-binding domain of the androgen receptor gene (l790p) associated with complete androgen insensitivity syndrome
Florina Raicu, Rossella Giuliani, Valentina Gatta, et al.
Diabetes Technology & Therapeutics
|
November 13, 2009
Insulin pump therapy management in very young children with type 1 diabetes using continuous subcutaneous insulin infusion
Ivana Rabbone, Andrea Scaramuzza, Adriana Bobbio, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 11, 2012
A case of congenital hypothyroidism in PHACE syndrome
Silvia Carinci, Stefano Tumini, Nicola Pietro Consilvio, et al.
Journal of Human Genetics
|
November 9, 2006
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay
Valentina Gatta, Ivana Antonucci, Elisena Morizio, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 16, 2010
Genital sanguineous discharge in prepuberty: a case of mullerian papilloma of vagina in a nine-year-old girl
Stefano Tumini, Silvia Carinci, Maria Teresa Anzellotti, et al.
Diabetes Research and Clinical Practice
|
January 20, 2009
Novel mutations in GCK and HNF1A genes in Italian families with MODY phenotype
Alessia Cappelli, Stefano Tumini, Agostino Consoli, et al.
Page
of 5