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Methods in Molecular Biology (Clifton, N.J.)
|
November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channel
Sarah E Flanagan, Sian Ellard
Indian Pediatrics
|
July 17, 2012
Permanent neonatal diabetes caused by a novel mutation
Vandana Jain, Sarah E Flanagan, Sian Ellard
Genetic Testing and Molecular Biomarkers
|
July 21, 2010
Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations
Sarah E Flanagan, Ann-Marie Patch, Sian Ellard
Reviews in Endocrine & Metabolic Disorders
|
October 6, 2010
Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11
Emma L Edghill, Sarah E Flanagan, Sian Ellard
Seminars in Pediatric Surgery
|
December 28, 2010
Genetics of congenital hyperinsulinemic hypoglycemia
Sarah E Flanagan, Ritika R Kapoor, Khalid Hussain
Methods in Molecular Biology (Clifton, N.J.)
|
October 13, 2010
Mutation surveyor: software for DNA sequence analysis
Jayne A L Minton, Sarah E Flanagan, Sian Ellard
Frontiers in Endocrinology
|
July 25, 2022
Congenital Hyperinsulinism: Current Laboratory-Based Approaches to the Genetic Diagnosis of a Heterogeneous Disease
Thomas I Hewat, Matthew B Johnson, Sarah E Flanagan
The Lancet. Diabetes & Endocrinology
|
July 31, 2016
Monogenic autoimmune diseases of the endocrine system
Matthew B Johnson, Andrew T Hattersley, Sarah E Flanagan
Nature Reviews. Endocrinology
|
April 16, 2026
The effect of hypoglycaemia on neurodevelopment: insights from congenital hyperinsulinism
Pamela Bowman, Jonna M E Männistö, Sarah E Flanagan
Indian Pediatrics
|
October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two Siblings
Amit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.
Page
of 23
Search research articles
Search
Showing results (1-10 of 229) with videos related to
Sort By:
Page
of 23
Methods in Molecular Biology (Clifton, N.J.)
|
November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channel
Sarah E Flanagan, Sian Ellard
Indian Pediatrics
|
July 17, 2012
Permanent neonatal diabetes caused by a novel mutation
Vandana Jain, Sarah E Flanagan, Sian Ellard
Genetic Testing and Molecular Biomarkers
|
July 21, 2010
Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations
Sarah E Flanagan, Ann-Marie Patch, Sian Ellard
Reviews in Endocrine & Metabolic Disorders
|
October 6, 2010
Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11
Emma L Edghill, Sarah E Flanagan, Sian Ellard
Seminars in Pediatric Surgery
|
December 28, 2010
Genetics of congenital hyperinsulinemic hypoglycemia
Sarah E Flanagan, Ritika R Kapoor, Khalid Hussain
Methods in Molecular Biology (Clifton, N.J.)
|
October 13, 2010
Mutation surveyor: software for DNA sequence analysis
Jayne A L Minton, Sarah E Flanagan, Sian Ellard
Frontiers in Endocrinology
|
July 25, 2022
Congenital Hyperinsulinism: Current Laboratory-Based Approaches to the Genetic Diagnosis of a Heterogeneous Disease
Thomas I Hewat, Matthew B Johnson, Sarah E Flanagan
The Lancet. Diabetes & Endocrinology
|
July 31, 2016
Monogenic autoimmune diseases of the endocrine system
Matthew B Johnson, Andrew T Hattersley, Sarah E Flanagan
Nature Reviews. Endocrinology
|
April 16, 2026
The effect of hypoglycaemia on neurodevelopment: insights from congenital hyperinsulinism
Pamela Bowman, Jonna M E Männistö, Sarah E Flanagan
Indian Pediatrics
|
October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two Siblings
Amit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.
Page
of 23