An Evaluation of Growth Hormone and IGF-1 Responses in Neonates with Hyperinsulinaemic Hypoglycaemia

by Senthil Senniappan, Khalid Hussain
Published 2013-01-01

A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome

by Devi Dayal, Dinesh Giri, Senthil Senniappan
Published 2017-03-01

The molecular mechanisms, diagnosis and management of congenital hyperinsulinism

by Senthil Senniappan, Ved Bhushan Arya, Khalid Hussain
Published 2013-01-01

Novel Splicing Mutation in B3GAT3 Associated with Short Stature, GH Deficiency, Hypoglycaemia, Developmental Delay, and Multiple Congenital Anomalies

by Samuel Bloor, Dinesh Giri, Mohammed Didi, Senthil Senniappan
Published 2017-01-01

Silent Crooke’s cell corticotroph adenoma of the pituitary gland presenting as delayed puberty

by Dinesh Giri, Federico Roncaroli, Ajay Sinha, Mohammed Didi, Senthil Senniappan
Published 2017-03-01

Congenital hyperinsulinism and Poland syndrome in association with 10p13–14 duplication

by Dinesh Giri, Prashant Patil, Rachel Hart, Mohammed Didi, Senthil Senniappan
Published 2017-03-01

Morphoproteomics and biomedical analytics coincide with clinical outcomes in supporting a constant but variable role for the mTOR pathway in the biology of congenital hyperinsulini...

by Robert E. Brown, Senthil Senniappan, Khalid Hussain, Mary F. McGuire
Published 2017-12-01

Congenital hyperinsulinism: diagnostic and management challenges in a developing country – case report

by Cheri Mathews John, Prakash Agarwal, Suriyakumar Govindarajulu, Sandhya Sundaram, Senthil Senniappan
Published 2017-12-01

Hepatoblastoma and Wilms’ tumour in an infant with Beckwith–Wiedemann syndrome and diazoxide resistant congenital hyperinsulinism

by Saurabh Uppal, James Blackburn, Mohammed Didi, Rajeev Shukla, James Hayden, Senthil Senniappan
Published 2019-02-01

The Efficacy of Denosumab in the Management of a Tibial Paediatric Aneurysmal Bone Cyst Compromised by Rebound Hypercalcaemia

by Matthew Harcus, Samantha Aldridge, Adesegun Abudu, Lee Jeys, Senthil Senniappan, Henry Morgan, Barry Pizer
Published 2020-01-01

Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control

by Dinesh Giri, Dona Pintus, Girvan Burnside, Atrayee Ghatak, Fulya Mehta, Princy Paul, Senthil Senniappan
Published 2017-09-01

Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism.

by Ved Bhushan Arya, Senthil Senniappan, Huseyin Demirbilek, Syeda Alam, Sarah E Flanagan, Sian Ellard, Khalid Hussain
Published 2014-01-01

A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular Carcinoma

by James Blackburn, Dinesh Giri, Barbara Ciolka, Nicole Gossan, Mohammad Didi, George Kokai, Alison Waghorn, Matthew Jones, Senthil Senniappan
Published 2018-01-01

Heterozygous Insulin Receptor <italic>(INSR)</italic> Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series

by Aashish Sethi, Nicola Foulds, Sarah Ehtisham, Syed Haris Ahmed, Jayne Houghton, Kevin Colclough, Mohammed Didi, Sarah E. Flanagan, Senthil Senniappan
Published 2020-12-01

Posaconazole-Induced Hypertension Masquerading as Congenital Adrenal Hyperplasia in a Child with Cystic Fibrosis

by Neha Agarwal, Louise Apperley, Norman F. Taylor, David R. Taylor, Lea Ghataore, Ellen Rumsby, Catherine Treslove, Richard Holt, Rebecca Thursfield, Senthil Senniappan
Published 2020-01-01

Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389.

by Daphne Yau, Thomas W Laver, Antonia Dastamani, Senthil Senniappan, Jayne A L Houghton, Guftar Shaikh, Tim Cheetham, Talat Mushtaq, Ritika R Kapoor, Tabitha Randell, Sian Ellard, Pratik Shah, Indraneel Banerjee, Sarah E Flanagan
Published 2020-01-01

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome [version 2; peer review: 2 approved, 1 approved with reservations]

by Indraneel Banerjee, Senthil Senniappan, Thomas W. Laver, Richard Caswell, Martin Zenker, Klaus Mohnike, Tim Cheetham, Matthew N. Wakeling, Dunia Ismail, Belinda Lennerz, Miranda Splitt, Merih Berberoğlu, Susann Empting, Martin Wabitsch, Simone Pötzsch, Pratik Shah, Zeynep Siklar, Charles F. Verge, Michael N. Weedon, Sian Ellard, Khalid Hussain, Sarah E. Flanagan
Published 2020-08-01