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Methods in Molecular Biology (Clifton, N.J.)
|
October 6, 2019
Diagnostic Genetic Testing for Monogenic Diabetes and Congenital Hyperinsulinemia
Jayne A L Houghton
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 8, 2019
A rare case of congenital hyperinsulinism (CHI) due to dual genetic aetiology involving HNF4A and ABCC8
Louise Apperley, Dinesh Giri, Jayne A L Houghton, et al.
Case Reports in Genetics
|
January 16, 2016
Mitchell-Riley Syndrome: A Novel Mutation in RFX6 Gene
Marta Zegre Amorim, Jayne A L Houghton, Sara Carmo, et al.
Frontiers in Endocrinology
|
January 1, 2025
Congenital hyperinsulinism in the Ukraine: a 10-year national study
Evgenia Globa, Henrik Thybo Christesen, Michael Bau Mortensen, et al.
Diabetes Research and Clinical Practice
|
May 17, 2017
A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up
Dragan Katanic, Ivana Vorgučin, Andrew Hattersley, et al.
Clinical Endocrinology
|
September 22, 2018
Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia
Thomas W Laver, Matthew N Wakeling, Janet Hong Yeow Hua, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 25, 2015
Neonatal diabetes in Ukraine: incidence, genetics, clinical phenotype and treatment
Evgenia Globa, Nataliya Zelinska, Deborah J G Mackay, et al.
Diabetologia
|
August 31, 2023
Bringing precision medicine to the management of pregnancy in women with glucokinase-MODY: a study of diagnostic accuracy and feasibility of non-invasive prenatal testing
Alice E Hughes, Jayne A L Houghton, Benjamin Bunce, et al.
Endocrine Connections
|
August 11, 2022
Spectrum of neuro-developmental disorders in children with congenital hyperinsulinism due to activating mutations in GLUD1
Sommayya Aftab, Diliara Gubaeva, Jayne A L Houghton, et al.
Reviews in Endocrine & Metabolic Disorders
|
March 19, 2020
Hyperinsulinemic hypoglycemia in children and adolescents: Recent advances in understanding of pathophysiology and management
Maria Gϋemes, Sofia Asim Rahman, Ritika R Kapoor, et al.
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Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 4
Methods in Molecular Biology (Clifton, N.J.)
|
October 6, 2019
Diagnostic Genetic Testing for Monogenic Diabetes and Congenital Hyperinsulinemia
Jayne A L Houghton
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 8, 2019
A rare case of congenital hyperinsulinism (CHI) due to dual genetic aetiology involving HNF4A and ABCC8
Louise Apperley, Dinesh Giri, Jayne A L Houghton, et al.
Case Reports in Genetics
|
January 16, 2016
Mitchell-Riley Syndrome: A Novel Mutation in RFX6 Gene
Marta Zegre Amorim, Jayne A L Houghton, Sara Carmo, et al.
Frontiers in Endocrinology
|
January 1, 2025
Congenital hyperinsulinism in the Ukraine: a 10-year national study
Evgenia Globa, Henrik Thybo Christesen, Michael Bau Mortensen, et al.
Diabetes Research and Clinical Practice
|
May 17, 2017
A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up
Dragan Katanic, Ivana Vorgučin, Andrew Hattersley, et al.
Clinical Endocrinology
|
September 22, 2018
Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia
Thomas W Laver, Matthew N Wakeling, Janet Hong Yeow Hua, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
July 25, 2015
Neonatal diabetes in Ukraine: incidence, genetics, clinical phenotype and treatment
Evgenia Globa, Nataliya Zelinska, Deborah J G Mackay, et al.
Diabetologia
|
August 31, 2023
Bringing precision medicine to the management of pregnancy in women with glucokinase-MODY: a study of diagnostic accuracy and feasibility of non-invasive prenatal testing
Alice E Hughes, Jayne A L Houghton, Benjamin Bunce, et al.
Endocrine Connections
|
August 11, 2022
Spectrum of neuro-developmental disorders in children with congenital hyperinsulinism due to activating mutations in GLUD1
Sommayya Aftab, Diliara Gubaeva, Jayne A L Houghton, et al.
Reviews in Endocrine & Metabolic Disorders
|
March 19, 2020
Hyperinsulinemic hypoglycemia in children and adolescents: Recent advances in understanding of pathophysiology and management
Maria Gϋemes, Sofia Asim Rahman, Ritika R Kapoor, et al.
Page
of 4