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)

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

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

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)

GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

Por De Franco, Elisa, Shaw-Smith, Charles, Flanagan, Sarah E., Shepherd, Maggie H., Hattersley, Andrew T., Ellard, Sian
Publicado em 2013

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism

Por Kapoor, Ritika R, Flanagan, Sarah E, Arya, Ved Bhushan, Shield, Julian P, Ellard, Sian, Hussain, Khalid
Publicado em 2013

Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism

Por Arya, Ved Bhushan, Senniappan, Senthil, Demirbilek, Huseyin, Alam, Syeda, Flanagan, Sarah E., Ellard, Sian, Hussain, Khalid
Publicado em 2014

Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia

Por Senniappan, Senthil, Sadeghizadeh, Atefeh, Flanagan, Sarah E, Ellard, Sian, Hashemipour, Mahin, Hosseinzadeh, Majid, Salehi, Mansour, Hussain, Khalid
Publicado no BMC Res Notes (2015)

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

Por Kocaay, Pınar, Şiklar, Zeynep, Ellard, Sian, Yagmurlu, Aydın, Çamtosun, Emine, Erden, Esra, Berberoglu, Merih, Flanagan, Sarah E.
Publicado no Horm Res Paediatr (2016)

Mutations of the Same Conserved Glutamate Residue in NBD2 of the Sulfonylurea Receptor 1 Subunit of the K(ATP) Channel Can Result in Either Hyperinsulinism or Neonatal Diabetes

Por Männikkö, Roope, Flanagan, Sarah E., Sim, Xiuli, Segal, David, Hussain, Khalid, Ellard, Sian, Hattersley, Andrew T., Ashcroft, Frances M.
Publicado em 2011

Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age

Por Arya, Ved Bhushan, Flanagan, Sarah E, Kumaran, Anitha, Shield, Julian P, Ellard, Sian, Hussain, Khalid, Kapoor, Ritika R
Publicado em 2013

Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk

Por Vedovato, Natascia, Cliff, Edward, Proks, Peter, Poovazhagi, Varadarajan, Flanagan, Sarah E., Ellard, Sian, Hattersley, Andrew T., Ashcroft, Frances M.
Publicado no Diabetologia (2016)

Galactokinase Deficiency in a Patient with Congenital Hyperinsulinism

Por Bayarchimeg, Mashbat, Ismail, Dunia, Lam, Amanda, Burk, Derek, Kirk, Jeremy, Hogler, Wolfgang, Flanagan, Sarah E, Ellard, Sian, Hussain, Khalid
Publicado em 2011