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Indraneel Banerjee

Showing results (131-140 of 150) with videos related to

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Journal of the Endocrine Society|May 20, 2022
Variation in Glycemic Outcomes in Focal Forms of Congenital Hyperinsulinism-The UK PerspectiveAntonia Dastamani, Daphne Yau, Clare Gilbert, et al.
Frontiers in Endocrinology|November 3, 2018
Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates With Histological Heterogeneity of Islet Cell LesionsRoss J Craigie, Maria Salomon-Estebanez, Daphne Yau, et al.
The Journal of Clinical Endocrinology and Metabolism|October 4, 2016
mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic SuccessMarie Szymanowski, Maria Salomon Estebanez, Raja Padidela, et al.
Hormone Research in Paediatrics|July 16, 2023
International Guidelines for the Diagnosis and Management of HyperinsulinismDiva D De Leon, Jean Baptiste Arnoux, Indraneel Banerjee, et al.
Diabetes|May 2, 2015
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-ChannelRachel J Salisbury, Bing Han, Rachel E Jennings, et al.
Frontiers in Endocrinology|May 19, 2025
Developing a congenital hyperinsulinism prioritized research agenda: a patient-driven international collaborative research networkTai L S Pasquini, Indraneel Banerjee, Henrik Thybo Christesen, et al.
Ebiomedicine|May 25, 2026
Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNAJasmin J Bennett, Thomas W Laver, Jonna M E Männistö, et al.
American Journal of Human Genetics|January 1, 2013
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activationSarah E Flanagan, Weijia Xie, Richard Caswell, et al.
Diabetes|April 27, 2017
Functional and Metabolomic Consequences of K<sub>ATP</sub> Channel Inactivation in Human IsletsChanghong Li, Amanda M Ackermann, Kara E Boodhansingh, et al.
Pediatric Diabetes|March 16, 2022
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this groupThomas I Hewat, Thomas W Laver, Jayne A L Houghton, et al.
Pageof 15

Showing results (131-140 of 150) with videos related to

Sort By:
Pageof 15
Journal of the Endocrine Society|May 20, 2022
Variation in Glycemic Outcomes in Focal Forms of Congenital Hyperinsulinism-The UK PerspectiveAntonia Dastamani, Daphne Yau, Clare Gilbert, et al.
Frontiers in Endocrinology|November 3, 2018
Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates With Histological Heterogeneity of Islet Cell LesionsRoss J Craigie, Maria Salomon-Estebanez, Daphne Yau, et al.
The Journal of Clinical Endocrinology and Metabolism|October 4, 2016
mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic SuccessMarie Szymanowski, Maria Salomon Estebanez, Raja Padidela, et al.
Hormone Research in Paediatrics|July 16, 2023
International Guidelines for the Diagnosis and Management of HyperinsulinismDiva D De Leon, Jean Baptiste Arnoux, Indraneel Banerjee, et al.
Diabetes|May 2, 2015
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-ChannelRachel J Salisbury, Bing Han, Rachel E Jennings, et al.
Frontiers in Endocrinology|May 19, 2025
Developing a congenital hyperinsulinism prioritized research agenda: a patient-driven international collaborative research networkTai L S Pasquini, Indraneel Banerjee, Henrik Thybo Christesen, et al.
Ebiomedicine|May 25, 2026
Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNAJasmin J Bennett, Thomas W Laver, Jonna M E Männistö, et al.
American Journal of Human Genetics|January 1, 2013
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activationSarah E Flanagan, Weijia Xie, Richard Caswell, et al.
Diabetes|April 27, 2017
Functional and Metabolomic Consequences of K<sub>ATP</sub> Channel Inactivation in Human IsletsChanghong Li, Amanda M Ackermann, Kara E Boodhansingh, et al.
Pediatric Diabetes|March 16, 2022
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this groupThomas I Hewat, Thomas W Laver, Jayne A L Houghton, et al.
Pageof 15