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E Flanagan

Showing results (121-130 of 582) with videos related to

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JCEM Case Reports|February 26, 2026
Congenital hyperinsulinism in an individual with CHARGE syndrome and a pathogenic <i>CHD7</i> variantConsuelo Ibeas, Franco Giraudo, Jonna M E Männistö, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 3, 2026
Modeling small vessel disease burden and vascular dementia likelihood from NACC dataAngelique D Gonzalez, Ali Ghaseminejad-Bandpey, Sudha Seshadri, et al.
Clinical Endocrinology|February 19, 2019
Hyperinsulinaemic hypoglycaemia: A new presentation of 16p11.2 deletion syndromeEirini Kostopoulou, Antonia Dastamani, Silvana Caiulo, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Congenital hyperinsulinism presenting with different clinical, biochemical and molecular genetic spectraEnver Şimşek, Çiğdem Binay, Sarah E Flanagan, et al.
Pediatric Diabetes|October 11, 2011
KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of lifeOscar Rubio-Cabezas, Sarah E Flanagan, Annet Damhuis, et al.
Endocrinology, Diabetes & Metabolism Case Reports|May 17, 2019
Exceptional diazoxide sensitivity in hyperinsulinaemic hypoglycaemia due to a novel HNF4A mutationVed Bhushan Arya, Jennifer Kalitsi, Ann Hickey, et al.
International Journal of Women'S Dermatology|July 5, 2021
A pilot evaluation of scalp skin wounding to promote hair growth in female pattern hair lossLaura J Burns, Dina Hagigeorges, Kelly E Flanagan, et al.
Human Mutation|January 26, 2013
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemiaKevin Colclough, Christine Bellanne-Chantelot, Cecile Saint-Martin, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal periodA M Patch, S E Flanagan, C Boustred, et al.
Frontiers in Endocrinology|June 2, 2012
Paternal Uniparental Isodisomy of Chromosome 11p15.5 within the Pancreas Causes Isolated Hyperinsulinemic HypoglycemiaS E Flanagan, R R Kapoor, V V Smith, et al.
Pageof 59

Showing results (121-130 of 582) with videos related to

Sort By:
Pageof 59
JCEM Case Reports|February 26, 2026
Congenital hyperinsulinism in an individual with CHARGE syndrome and a pathogenic <i>CHD7</i> variantConsuelo Ibeas, Franco Giraudo, Jonna M E Männistö, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|April 3, 2026
Modeling small vessel disease burden and vascular dementia likelihood from NACC dataAngelique D Gonzalez, Ali Ghaseminejad-Bandpey, Sudha Seshadri, et al.
Clinical Endocrinology|February 19, 2019
Hyperinsulinaemic hypoglycaemia: A new presentation of 16p11.2 deletion syndromeEirini Kostopoulou, Antonia Dastamani, Silvana Caiulo, et al.
The Turkish Journal of Pediatrics|March 1, 2014
Congenital hyperinsulinism presenting with different clinical, biochemical and molecular genetic spectraEnver Şimşek, Çiğdem Binay, Sarah E Flanagan, et al.
Pediatric Diabetes|October 11, 2011
KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of lifeOscar Rubio-Cabezas, Sarah E Flanagan, Annet Damhuis, et al.
Endocrinology, Diabetes & Metabolism Case Reports|May 17, 2019
Exceptional diazoxide sensitivity in hyperinsulinaemic hypoglycaemia due to a novel HNF4A mutationVed Bhushan Arya, Jennifer Kalitsi, Ann Hickey, et al.
International Journal of Women'S Dermatology|July 5, 2021
A pilot evaluation of scalp skin wounding to promote hair growth in female pattern hair lossLaura J Burns, Dina Hagigeorges, Kelly E Flanagan, et al.
Human Mutation|January 26, 2013
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha and 4 alpha in maturity-onset diabetes of the young and hyperinsulinemic hypoglycemiaKevin Colclough, Christine Bellanne-Chantelot, Cecile Saint-Martin, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal periodA M Patch, S E Flanagan, C Boustred, et al.
Frontiers in Endocrinology|June 2, 2012
Paternal Uniparental Isodisomy of Chromosome 11p15.5 within the Pancreas Causes Isolated Hyperinsulinemic HypoglycemiaS E Flanagan, R R Kapoor, V V Smith, et al.
Pageof 59