Comment on: Khurana et al. The Diagnosis of Neonatal Diabetes in a Mother at 25 Years of Age. Diabetes Care 2012;35:e59

Por Chakera, Ali J., Flanagan, Sarah E., Ellard, Sian, Hattersley, Andrew T.
Publicado em 2013

Anemia in a Child with Deafness: Be Vigilant for a Rare Cause!

Por Ramzan, Mohammed, Flanagan, Sarah E., Ellard, Sian, Yadav, Satya P.
Publicado no Indian J Hematol Blood Transfus (2014)

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

Por Güven, Ayla, Cebeci, Ayşe Nurcan, Ellard, Sian, Flanagan, Sarah E.
Publicado no J Clin Res Pediatr Endocrinol (2016)

Nifedipine in Congenital Hyperinsulinism- A Case Report

Por Khawash, Papiya, Hussain, Khalid, Flanagan, Sarah E., Chatterjee, Sudip, Basak, Dhananjoy
Publicado no J Clin Res Pediatr Endocrinol (2015)

Genetic Mechanisms Highlight Shared Pathways for the Pathogenesis of Polygenic Type 1 Diabetes and Monogenic Autoimmune Diabetes

Por Johnson, Matthew B., Cerosaletti, Karen, Flanagan, Sarah E., Buckner, Jane H.
Publicado no Curr Diab Rep (2019)

Two decades since the fetal insulin hypothesis: what have we learned from genetics?

Por Hughes, Alice E., Hattersley, Andrew T., Flanagan, Sarah E., Freathy, Rachel M.
Publicado no Diabetologia (2021)

Prematurity, macrosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation

Por Khoriati, Dana, Arya, Ved Bhushan, Flanagan, Sarah E, Ellard, Sian, Hussain, Khalid
Publicado em 2013

A Combination of Nifedipine and OctreotideTreatment in an HyperinsulinemicHypoglycemic Infant

Por Durmaz, Erdem, Flanagan, Sarah E., Parlak, Mesut, Ellard, Sian, Akcurin, Sema, Bircan, İffet
Publicado em 2014

Exceptional diazoxide sensitivity in hyperinsulinaemic hypoglycaemia due to a novel HNF4A mutation

Por Arya, Ved Bhushan, Kalitsi, Jennifer, Hickey, Ann, Flanagan, Sarah E, Kapoor, Ritika R
Publicado no Endocrinol Diabetes Metab Case Rep (2019)

Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptoms

Por Männikkö, Roope, Jefferies, Craig, Flanagan, Sarah E., Hattersley, Andrew, Ellard, Sian, Ashcroft, Frances M.
Publicado em 2010

Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation

Por Işık, Emregül, Demirbilek, Hüseyin, Houghton, Jayne A., Ellard, Sian, Flanagan, Sarah E., Hussain, Khalid
Publicado no J Clin Res Pediatr Endocrinol (2019)

3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency and Hyperinsulinemic Hypoglycemia: Characterization of a Novel Mutation and Severe Dietary Protein Sensitivity

Por Kapoor, Ritika R., James, Chela, Flanagan, Sarah E., Ellard, Sian, Eaton, Simon, Hussain, Khalid
Publicado no J Clin Endocrinol Metab (2009)

Transient Neonatal Diabetes Mellitus in a Turkish Patient with Three Novel Homozygous Variants in the ZFP57 Gene

Por Boyraz, Mehmet, Ulucan, Korkut, Taşkın, Necati, Akçay, Teoman, Flanagan, Sarah E., Mackay, Deborah J.G.
Publicado em 2013

Neurogenin 3 is important but not essential for pancreatic islet development in humans

Por Rubio-Cabezas, Oscar, Codner, Ethel, Flanagan, Sarah E., Gómez, José L., Ellard, Sian, Hattersley, Andrew T.
Publicado em 2014

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

Por Çamtosun, Emine, Flanagan, Sarah E., Ellard, Sian, Şıklar, Zeynep, Hussain, Khalid, Kocaay, Pınar, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2015)

Case report: maternal mosaicism resulting in inheritance of a novel GATA6 mutation causing pancreatic agenesis and neonatal diabetes mellitus

Por Yau, Daphne, De Franco, Elisa, Flanagan, Sarah E., Ellard, Sian, Blumenkrantz, Miriam, Mitchell, John J.
Publicado no Diagn Pathol (2017)

Analysis of large scale sequencing cohorts does not support the role of variants in UCP2 as a cause of hyperinsulinaemic hypoglycaemia

Por Laver, Thomas W, Weedon, Michael N, Caswell, Richard, Hussain, Khalid, Ellard, Sian, Flanagan, Sarah E
Publicado no Hum Mutat (2017)

A Novel HNF4A Mutation Causing Three Phenotypic Forms of Glucose Dysregulation in a Family

Por Chandran, Suresh, Rajadurai, Victor Samuel, Hoi, Wai Han, Flanagan, Sarah E., Hussain, Khalid, Yap, Fabian
Publicado no Front Pediatr (2020)

Effective treatment with oral sulfonylureas in patients with diabetes due to SUR1 Mutations

Por Rafiq, Meena, Flanagan, Sarah E., Patch, Ann-Marie, Shields, Beverley M., Ellard, Sian, Hattersley, Andrew T.
Publicado no Diabetes Care (2008)

Sulfonylurea Treatment in Young Children with Neonatal Diabetes: Dealing with Hyperglycaemia, Hypoglycaemia and Sickdays

Por Codner, Ethel, Flanagan, Sarah E., Ugarte, Francisca, García, Hernán, Vidal, Teresa, Ellard, Sian, Hattersley, Andrew T.
Publicado no Diabetes Care (2007)