S. Senniappan

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Sirolimus in severe hyperinsulinemic hypoglycemia.

Robert E. Brown, K. Hussain, S. Senniappan, 2014, The New England journal of medicine.

An eHealth Framework for Managing Pediatric Growth Disorders and Growth Hormone Therapy

L. Fernández-Luque, T. Reinehr, S. Senniappan, 2021, Journal of medical Internet research.

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

S. Senniappan, G. Burnside, D. Giri, 2017, BMC Research Notes.

Mode of clinical presentation and delayed diagnosis of Turner syndrome: a single Centre UK study

S. Senniappan, J. Blair, M. Didi, 2018, International Journal of Pediatric Endocrinology.

Obesity is common at diagnosis of childhood pituitary adenoma and may persist following successful treatment

S. Senniappan, J. Blair, C. Daousi, 2019, Clinical endocrinology.

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

K. Hussain, S. Senniappan, 2013, International journal of endocrinology.

Denosumab Therapy for Refractory Hypercalcemia Secondary to Squamous Cell Carcinoma of Skin in Epidermolysis Bullosa

S. Senniappan, L. Brook, J. Hayden, 2015, World journal of oncology.

Biochemical studies in patients with hyperinsulinaemic hypoglycaemia

S. Alam, K. Hussain, S. Senniappan, 2013, European Journal of Pediatrics.

Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutation

S. Ellard, S. Flanagan, K. Hussain, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Sirolimus therapy in infants with severe hyperinsulinemic hypoglycemia.

Robert E. Brown, S. Ellard, S. Flanagan, 2014, The New England journal of medicine.

HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin response

S. Ellard, S. Flanagan, K. Hussain, 2014, Diabetic medicine : a journal of the British Diabetic Association.

Idiopathic postprandial hyperinsulinaemic hypoglycaemia

K. Hussain, S. Senniappan, M. Güemes, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Insight into hypoglycemia frequency in congenital hyperinsulinism: evaluation of a large UK CGM dataset

S. Senniappan, I. Banerjee, K. Cosgrove, 2022, BMJ Open Diabetes Research & Care.

Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management

S. Senniappan, K. Hawton, D. Giri, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Diazoxide‐induced pulmonary hypertension in hyperinsulinaemic hypoglycaemia: Recommendations from a multicentre study in the United Kingdom

A. Giardini, L. Hunter, S. Senniappan, 2019, Clinical endocrinology.

Chromosome 6q24 transient neonatal diabetes mellitus and protein sensitive hyperinsulinaemic hypoglycaemia

S. Ellard, S. Flanagan, K. Hussain, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

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

S. Senniappan, F. Roncaroli, M. Didi, 2017, Endocrinology, diabetes & metabolism case reports.

Use of Long-Acting Somatostatin Analogue (Lanreotide) in an Adolescent with Diazoxide-Responsive Congenital Hyperinsulinism and Its Psychological Impact

K. Hussain, S. Senniappan, R. Amin, 2015, Hormone Research in Paediatrics.

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

S. Flanagan, J. Houghton, S. Senniappan, 2020, Journal of clinical research in pediatric endocrinology.

13q Deletion in a Girl Contributing to Antenatal Stroke, Insulin Resistance and Lymphedema Praecox: Expanding the Clinical Spectrum

K. Hussain, S. Senniappan, C. Ponmani, 2015 .

Neonatal Hypoglycemia

K. Hussain, S. Senniappan, V. Arya, 2013, The Indian Journal of Pediatrics.

Fluoxetine-Induced Hypoglycaemia in a Patient with Congenital Hyperinsulinism on Lanreotide Therapy

S. Senniappan, M. Didi, D. Giri, 2015, Journal of clinical research in pediatric endocrinology.

Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency

D. Rigden, S. Senniappan, M. Peak, 2017, International Journal of Pediatric Endocrinology.

The hypoglycaemia error grid: A UK-wide consensus on CGM accuracy assessment in hyperinsulinism

S. Senniappan, I. Banerjee, M. Dunne, 2022, Frontiers in Endocrinology.

Paradoxical Hypoglycaemia Associated with Diazoxide Therapy for Hyperinsulinaemic Hypoglycaemia

K. Hussain, S. Senniappan, Hannah Gannon, 2013, Hormone Research in Paediatrics.

Pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus (PHID) syndrome is associated with severe chronic inflammation and cardiomyopathy, and represents a new monogenic autoinflammatory syndrome

K. Hussain, J. Kaski, S. Senniappan, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

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

S. Senniappan, M. Didi, D. Giri, 2017, Case reports in genetics.

Dipeptidyl peptidase-4 expression in pancreatic tissue from patients with congenital hyperinsulinism.

K. Hussain, S. Senniappan, S. Rahman, 2015, International journal of clinical and experimental pathology.

Continuous Flash Glucose Monitoring in children with Congenital Hyperinsulinism; first report on accuracy and patient experience

S. Senniappan, M. Didi, L. Turner, 2018, International Journal of Pediatric Endocrinology.

AUTHOR COPY ONLY Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11

S. Ellard, S. Alam, S. Flanagan, 2014 .

45,X male – rare case of unbalanced translocation of Y chromosome to chromosome 2 presenting with developmental delay, learning difficulty and obesity

S. Senniappan, L. Apperley, J. Suntharesan, 2022, Endocrinology, diabetes & metabolism case reports.

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

S. Senniappan, M. Harcus, B. Pizer, 2020, Case reports in pediatrics.

Intrafamilial Phenotypic Variability and Consequences of Non-Compliance with Treatment in Congenital Adrenal Hyperplasia and Congenital Hypothyroidism within a Single Family 

M. Dattani, S. Senniappan, A. Barnicoat, 2017, Hormone Research in Paediatrics.

Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities

S. Senniappan, M. Peak, P. McNamara, 2017, Human molecular genetics.

The molecular mechanisms, diagnosis and management of congenital hyperinsulinism

K. Hussain, S. Senniappan, V. Arya, 2013, Indian journal of endocrinology and metabolism.

Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management

K. Hussain, S. Senniappan, C. James, 2012, Journal of Inherited Metabolic Disease.

Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.

S. Ellard, S. Alam, S. Flanagan, 2014, European journal of endocrinology.

Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC 8 / KCNJ 11 mutations

S. Ellard, S. Alam, S. Flanagan, 2014 .

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

S. Senniappan, D. Dayal, D. Giri, 2017, Annals of pediatric endocrinology & metabolism.

Hepatoblastoma and Wilms' tumour in an infant with Beckwith-Wiedemann syndrome and diazoxide resistant congenital hyperinsulinism.

J. Blackburn, S. Senniappan, R. Shukla, 2019, Endocrinology, diabetes & metabolism case reports.

The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation

K. Hussain, S. Senniappan, C. Beesley, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

The effect of socioeconomic deprivation on efficacy of continuous subcutaneous insulin infusion: a retrospective paediatric case-controlled survey

S. Senniappan, R. Amin, Claire Smith, 2011, European Journal of Pediatrics.

Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing

S. Bhaskar, S. Banka, S. Douzgou, 2017, Archives of Disease in Childhood.

Gonadotrophin-Independent Precocious Puberty Associated with Later Diagnosis of Testicular Embryonal Carcinoma

M. Dattani, A. Freeman, S. Senniappan, 2012, Hormone Research in Paediatrics.

Postprandial Hyperinsulinaemic Hypoglycaemia Secondary to a Congenital Portosystemic Shunt

M. Davenport, K. Hussain, A. Dhawan, 2015, Hormone Research in Paediatrics.

Insulin oedema in a child with newly diagnosed diabetes mellitus

S. Senniappan, Claire Smith, C. Gardner, 2014, European Journal of Pediatrics.

Glycolate oxidase deficiency in a patient with congenital hyperinsulinism and unexplained hyperoxaluria

S. Senniappan, G. Rumsby, M. Didi, 2017, Pediatric Nephrology.

Klinefelter syndrome: going beyond the diagnosis

U. Srirangalingam, S. Senniappan, R. Mitchell, 2022, Archives of Disease in Childhood.

Clinical profile and outcome of infantile onset diabetes mellitus in southern India

V. Mohan, V. Radha, S. Senniappan, 2013, Indian Pediatrics.

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

G. Kokai, J. Blackburn, S. Senniappan, 2018, Case reports in genetics.

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

S. Senniappan, Prashant Patil, M. Didi, 2017, Endocrinology, diabetes & metabolism case reports.

Variations in sex steroid priming for growth hormone stimulation testing in UK

S. Senniappan, C. Frerichs, L. Raymond, 2016, Archives of Disease in Childhood.

Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations

S. Senniappan, D. Bockenhauer, J. Achermann, 2020, Hormone Research in Paediatrics.

Childhood obesity: A review of current and future management options

J. Blackburn, S. Senniappan, Lucy Gait, 2021, Clinical endocrinology.

Variation in Glycemic Outcomes in Focal Forms of Congenital Hyperinsulinism—The UK Perspective

P. de Coppi, S. Flanagan, J. Houghton, 2022, Journal of the Endocrine Society.

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

S. Senniappan, S. Sundaram, C. John, 2017, Annals of pediatric endocrinology & metabolism.

Hypercalcaemic Pancreatitis, Adrenal Insufficiency, Autoimmune Thyroiditis and Diabetes Mellitus in a girl with Probable Sarcoidosis

S. Senniappan, D. Dayal, L. Mccann, 2017, International journal of endocrinology and metabolism.

Flash glucose monitoring in children with congenital hyperinsulinism; first report on accuracy and patient experience

S. Senniappan, M. Didi, L. Turner, 2016 .

Testosterone Therapy Improves the First Year Height Velocity in Adolescent Boys with Constitutional Delay of Growth and Puberty

S. Senniappan, J. Blair, Prashant Patil, 2017, International journal of endocrinology and metabolism.

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

S. Senniappan, G. Burnside, D. Giri, 2017, BMC Research Notes.

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

Mary F. McGuire, Robert E. Brown, K. Hussain, 2017, Orphanet Journal of Rare Diseases.

Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family

S. Ellard, S. Flanagan, K. Hussain, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

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

S. Ellard, S. Alam, S. Flanagan, 2014, PloS one.

Burosumab Therapy in a Paediatric Patient with McCune-Albright Syndrome: A Case Report

S. Senniappan, L. Apperley, 2022, Hormone Research in Paediatrics.

Case 2: Fractures in under‐6‐month‐old exclusively breast‐fed infants born to immigrant parents: nonaccidental injury? (Discussion and Diagnosis)

S. Senniappan, M. Mughal, I. Doughty, 2008 .

Endocrine Abstracts vol 45

S. Senniappan, A. Morris, A. Ghatak, 2016 .

Successful transition to sulfonylurea therapy in two Iraqi siblings with neonatal diabetes mellitus and iDEND syndrome due to ABCC8 mutation

S. Senniappan, D. Giri, E. Ozsu, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

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

S. Ellard, T. Laver, S. Flanagan, 2020, PloS one.

Deprivation impedes success of insulin intensification in children and adolescents with Type 1 diabetes; longitudinal linear mixed modelling of a retrospective observational cohort

S. Senniappan, R. Amin, P. Hine, 2010, Diabetic medicine : a journal of the British Diabetic Association.

Clinical Presentation and Long Term Outcome of 40 children with Infantile Onset Diabetes Mellitus in South India

Mohan, Radha, S. Senniappan, 2013 .

Congenital hyperinsulinism due to mutations in HNF1A.

N. Canham, S. Senniappan, I. Banerjee, 2020, European journal of medical genetics.

A rare case of congenital hyperinsulinism (CHI) due to dual genetic aetiology involving HNF4A and ABCC8

S. Flanagan, J. Houghton, S. Senniappan, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

Isolated premature menarche in two siblings with Neurofibromatosis type 1

J. Blackburn, S. Senniappan, M. Didi, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Genomic and morphoproteomic correlates implicate the IGF-1/mTOR/Akt pathway in the pathogenesis of diffuse congenital hyperinsulinism

Robert E. Brown, K. Hussain, S. Senniappan, 2016 .

Idiopathic intracranial hypertension in children with obesity

S. Senniappan, Ram S. Kumar, L. Apperley, 2022, Acta paediatrica.

Case 2: Fractures in under‐6‐month‐old exclusively breast‐fed infants born to immigrant parents: nonaccidental injury? (Case Presentation)

S. Senniappan, M. Mughal, I. Doughty, 2008, Acta paediatrica.

Effect of Growth Hormone Therapy in Patients with Noonan Syndrome: A Retrospective Study

S. Senniappan, J. Blair, M. Didi, 2020, International journal of endocrinology and metabolism.

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

M. Weedon, S. Ellard, M. Wabitsch, 2020, Wellcome open research.

Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution

S. Senniappan, D. Giri, A. Brandt, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Congenital Hyperinsulinism and Cochlear Hypoplasia in a Rare Case of Pallister-Hall Syndrome

S. Senniappan, A. Weber, S. Avula, 2015 .

Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia

S. Ellard, M. Hashemipour, S. Flanagan, 2015, BMC Research Notes.

Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus

J. Houghton, S. Senniappan, I. Banerjee, 2023, Frontiers in Endocrinology.