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Diabetologia
|
June 16, 2011
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
R R Kapoor, S E Flanagan, C T James, et al.
BMJ Open Diabetes Research & Care
|
November 14, 2024
Widening the phenotypic spectrum caused by pathogenic <i>PDX1</i> variants in individuals with neonatal diabetes
Nicola Jeffery, Omar Al Nimri, Jayne A L Houghton, et al.
Regulatory Peptides
|
December 26, 2006
Gender differences in the relationship between leptin, insulin resistance and the autonomic nervous system
Daniel E Flanagan, Julian C Vaile, Graham W Petley, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
May 17, 2016
A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus
Sevim Ünal, Deniz Gönülal, Ahmet Uçaktürk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 29, 2021
Monogenic diabetes in Pakistani infants and children: challenges in a resource poor country
Mohsina Noor Ibrahim, Taj Muhammad Laghari, Miara Riaz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 22, 2011
Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees
Sarah E Flanagan, Ann-Marie Patch, Jonathan M Locke, et al.
Journal of Autism and Developmental Disorders
|
April 3, 2019
Types of Services and Costs of Programs for Preschoolers with Autism Spectrum Disorder Across Sectors: A Comparison of Two Canadian Provinces
Kate Tsiplova, Wendy J Ungar, Helen E Flanagan, et al.
Journal of Biomedical Optics
|
August 17, 2012
Out-of-plane Stokes imaging polarimeter for early skin cancer diagnosis
Pejhman Ghassemi, Paul Lemaillet, Thomas A Germer, et al.
EMBO Molecular Medicine
|
January 27, 2023
Infancy-onset diabetes caused by de-regulated AMPylation of the human endoplasmic reticulum chaperone BiP
Luke A Perera, Andrew T Hattersley, Heather P Harding, et al.
Journal of Neuropathology and Experimental Neurology
|
December 2, 2022
What every neuropathologist needs to know: condensed protocol work-up for clinical dementia syndromes
Rachel A Multz, Callen Spencer, Arleen Matos, et al.
Page
of 59
Search research articles
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Showing results (371-380 of 582) with videos related to
Sort By:
Page
of 59
Diabetologia
|
June 16, 2011
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
R R Kapoor, S E Flanagan, C T James, et al.
BMJ Open Diabetes Research & Care
|
November 14, 2024
Widening the phenotypic spectrum caused by pathogenic <i>PDX1</i> variants in individuals with neonatal diabetes
Nicola Jeffery, Omar Al Nimri, Jayne A L Houghton, et al.
Regulatory Peptides
|
December 26, 2006
Gender differences in the relationship between leptin, insulin resistance and the autonomic nervous system
Daniel E Flanagan, Julian C Vaile, Graham W Petley, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
May 17, 2016
A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus
Sevim Ünal, Deniz Gönülal, Ahmet Uçaktürk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 29, 2021
Monogenic diabetes in Pakistani infants and children: challenges in a resource poor country
Mohsina Noor Ibrahim, Taj Muhammad Laghari, Miara Riaz, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 22, 2011
Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees
Sarah E Flanagan, Ann-Marie Patch, Jonathan M Locke, et al.
Journal of Autism and Developmental Disorders
|
April 3, 2019
Types of Services and Costs of Programs for Preschoolers with Autism Spectrum Disorder Across Sectors: A Comparison of Two Canadian Provinces
Kate Tsiplova, Wendy J Ungar, Helen E Flanagan, et al.
Journal of Biomedical Optics
|
August 17, 2012
Out-of-plane Stokes imaging polarimeter for early skin cancer diagnosis
Pejhman Ghassemi, Paul Lemaillet, Thomas A Germer, et al.
EMBO Molecular Medicine
|
January 27, 2023
Infancy-onset diabetes caused by de-regulated AMPylation of the human endoplasmic reticulum chaperone BiP
Luke A Perera, Andrew T Hattersley, Heather P Harding, et al.
Journal of Neuropathology and Experimental Neurology
|
December 2, 2022
What every neuropathologist needs to know: condensed protocol work-up for clinical dementia syndromes
Rachel A Multz, Callen Spencer, Arleen Matos, et al.
Page
of 59