Articles with public access mandates - Dr Senthil SenniappanLearn more
Not available anywhere: 7
Neonatal hypoglycemia
VB Arya, S Senniappan, M Guemes, K Hussain
The Indian Journal of Pediatrics 81, 58-65, 2014
Mandates: UK Medical Research Council
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutation
P Shah, VB Arya, SE Flanagan, K Morgan, S Ellard, S Senniappan, ...
Journal of Pediatric Endocrinology and Metabolism 28 (5-6), 695-699, 2015
Mandates: UK Medical Research Council, Wellcome Trust
Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family
O Babiker, SE Flanagan, S Ellard, HA Girim, K Hussain, S Senniappan
Journal of Pediatric Endocrinology and Metabolism 28 (9-10), 1073-1077, 2015
Mandates: Wellcome Trust
Biochemical studies in patients with hyperinsulinaemic hypoglycaemia
H Al-Otaibi, S Senniappan, S Alam, K Hussain
European journal of pediatrics 172, 1435-1440, 2013
Mandates: UK Medical Research Council
The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation
S Senniappan, D Ismail, C Shipster, C Beesley, K Hussain
Journal of Pediatric Endocrinology and Metabolism 28 (1-2), 83-86, 2015
Mandates: UK Medical Research Council
Paradoxical hypoglycaemia associated with diazoxide therapy for hyperinsulinaemic hypoglycaemia
C Ponmani, H Gannon, K Hussain, S Senniappan
Hormone Research in Paediatrics 80 (2), 129-133, 2013
Mandates: UK Medical Research Council
Heterozygous CDC73 mutation causing hyperparathyroidism in children and adolescents: a report of 2 cases
J Blackburn, I Mulvey, R Nadar, RP Dias, V Saraff, S Senniappan
Journal of Pediatric Endocrinology and Metabolism 35 (12), 1547-1551, 2022
Mandates: US National Institutes of Health, UK Medical Research Council
Available somewhere: 21
Sirolimus therapy in infants with severe hyperinsulinemic hypoglycemia
S Senniappan, S Alexandrescu, N Tatevian, P Shah, V Arya, S Flanagan, ...
New England Journal of Medicine 370 (12), 1131-1137, 2014
Mandates: UK Medical Research Council
Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism
VB Arya, S Senniappan, H Demirbilek, S Alam, SE Flanagan, S Ellard, ...
PloS one 9 (5), e98054, 2014
Mandates: UK Medical Research Council
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities
D Giri, ML Vignola, A Gualtieri, V Scagliotti, P McNamara, M Peak, M Didi, ...
Human molecular genetics 26 (22), 4315-4326, 2017
Mandates: UK Medical Research Council, Wellcome Trust
Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing
A Ghosh, H Schlecht, LE Heptinstall, JK Bassett, E Cartwright, SS Bhaskar, ...
Archives of Disease in Childhood 102 (11), 1019-1029, 2017
Mandates: National Institute for Health Research, UK
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations
VB Arya, M Guemes, A Nessa, S Alam, P Shah, C Gilbert, S Senniappan, ...
European journal of endocrinology 171 (6), 685-695, 2014
Mandates: UK Medical Research Council, Wellcome Trust
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity‐onset diabetes of the young, and incretin response
VB Arya, S Rahman, S Senniappan, SE Flanagan, S Ellard, K Hussain
Diabetic Medicine 31 (3), e11-e15, 2014
Mandates: UK Medical Research Council, Wellcome Trust
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
D Yau, TW Laver, A Dastamani, S Senniappan, JAL Houghton, G Shaikh, ...
PLoS One 15 (2), e0228417, 2020
Mandates: Wellcome Trust, Royal Society UK
Klinefelter syndrome: going beyond the diagnosis
G Butler, U Srirangalingam, J Faithfull, P Sangster, S Senniappan, ...
Archives of disease in childhood 108 (3), 166-171, 2023
Mandates: UK Medical Research Council
An eHealth framework for managing pediatric growth disorders and growth hormone therapy
P Dimitri, L Fernandez-Luque, I Banerjee, I Bergadá, LE Calliari, ...
Journal of medical Internet research 23 (5), e27446, 2021
Mandates: National Institute for Health Research, UK
Heterozygous insulin receptor (INSR) mutation associated with neonatal hyperinsulinemic hypoglycaemia and familial diabetes mellitus: case series
A Sethi, N Foulds, S Ehtisham, SH Ahmed, J Houghton, K Colclough, ...
J Clin Res Pediatr Endocrinol 12 (4), 420-6, 2020
Mandates: Wellcome Trust, Royal Society UK
Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia
S Senniappan, A Sadeghizadeh, SE Flanagan, S Ellard, M Hashemipour, ...
BMC research notes 8, 1-8, 2015
Mandates: Wellcome Trust
Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus
MG Shaikh, AK Lucas-Herald, A Dastamani, M Salomon Estebanez, ...
Frontiers in Endocrinology 14, 1231043, 2023
Mandates: National Institute for Health Research, UK
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
I Banerjee, S Senniappan, TW Laver, R Caswell, M Zenker, K Mohnike, ...
Wellcome Open Research 4, 2019
Mandates: US National Institutes of Health, Wellcome Trust, Royal Society UK
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