M. Didi

发表

A. Ogilvy-Stuart, S. Shalet, E. Crowne, 1986, Bailliere's clinical endocrinology and metabolism.

High incidence of obesity in young adults after treatment of acute lymphoblastic leukemia in childhood.

A. Ogilvy-Stuart, S. Shalet, J. Wales, 1995, The Journal of pediatrics.

Growth, puberty and obesity after treatment for leukaemia

A. Ogilvy-Stuart, S. Shalet, S. Shalet, 1995, Acta paediatrica (Oslo, Norway : 1992). Supplement.

The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism.

S. Ellard, P. Clayton, S. Flanagan, 2011, European journal of endocrinology.

Growth Hormone Replacement in an Adult with Mild Growth Hormone Deficiency and Hereditary Motor and Sensory Neuropathy: Growth Hormone Restores Independent Mobility

S. Shalet, M. Didi, A. Toogood, 1998, Hormone Research in Paediatrics.

The Challenges of Cortisol Replacement Therapy in Childhood: Observations from a Case Series of Children Treated with Modified-Release Hydrocortisone

J. Blair, P. Newland, M. Peak, 2018, Pediatric Drugs.

Delayed and Precocious Puberty

J. Blair, L. Abernethy, Julie Smith, 2011 .

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.

Phaeochromocytoma in children

R. Armstrong, L. Howell, P. Losty, 2008, Archives of Disease in Childhood.

TIPIT: A randomised controlled trial of thyroxine in preterm infants under 28 weeks gestation: Magnetic Resonance Imaging and Magnetic Resonance Angiography protocol

C. Gamble, A. Tietze, L. Gregory, 2008, BMC pediatrics.

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

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

A novel method of collection of saliva for estimation of steroid levels in extremely premature infants

S. Victor, M. Turner, J. Drury, 2013, Acta paediatrica.

Selecting girls with precocious puberty for brain imaging: validation of European evidence-based diagnosis rule.

M. Cisternino, W. Sippell, D. Mul, 2003, The Journal of pediatrics.

Effect of thyroxine on brain microstructure in extremely premature babies: magnetic resonance imaging findings in the TIPIT study

C. Gamble, A. Tietze, L. Parkes, 2014, Pediatric Radiology.

Functional characterization of a novel insulin receptor mutation contributing to Rabson–Mendenhall syndrome

M. Soos, A. Tuthill, E. Sweeney, 2006, Clinical endocrinology.

The neuroendocrine sequelae of paediatric craniopharyngioma: a 40-year meta-data analysis of 185 cases from three UK centres.

M. Gaze, P. Clayton, L. Patel, 2017, European journal of endocrinology.

Concentrations of leptin, adiponectin and other metabolic parameters in non-obese children with Down syndrome

N. Sachdeva, S. Attri, D. Dayal, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Head circumference and linear growth during the first 3 years in treated congenital hypothyroidism in relation to aetiology and initial biochemical severity

S. C. Wong, M. Didi, S. Ng, 2004, Clinical endocrinology.

Multivariate analyses of factors that affect neonatal screening thyroid stimulating hormone

S. C. Wong, D. Isherwood, E. Chakkarapani, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Early morning salivary cortisol and cortisone, and adrenal responses to a simplified low‐dose short Synacthen test in children with asthma

G. Lancaster, J. Blair, J. Couriel, 2014, Clinical endocrinology.

Thyroid function at diagnosis of type I diabetes

D. Isherwood, M. Didi, H. Payne, 2010, Archives of Disease in Childhood.

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

V. Tillmann, P. Chanson, M. Dattani, 2020, Orphanet Journal of Rare Diseases.

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.

Pubertal growth in response to testosterone replacement therapy for radiation-induced Leydig cell failure.

H. Gattamaneni, S. Shalet, P. Morris-Jones, 1994, Medical and pediatric oncology.

Open resection of hypothalamic hamartomas for intractable epilepsy revisited, using intraoperative MRI

J. Blair, T. Martland, C. Mallucci, 2018, Child's Nervous System.

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.

A preliminary trial of the effect of recombinant human growth hormone on short‐term linear growth and glucose homeostasis in children with Crohn’s disease

S. Ahmed, P. Mcgrogan, A. Dalzell, 2011, Clinical endocrinology.

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.

Pituitary adenomas in childhood, adolescence and young adulthood: presentation, management, endocrine and metabolic outcomes.

D. Cuthbertson, C. Daousi, M. Javadpour, 2010, European journal of endocrinology.

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.

Adrenal responses to a low‐dose short synacthen test in children with asthma

M. Pirmohamed, R. Smyth, A. Jorgensen, 2011, Clinical endocrinology.

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.

Management of craniopharyngioma: the Liverpool experience following the introduction of the CCLG guidelines. Introducing a new risk assessment grading system

J. Blair, B. Pizer, C. Mallucci, 2012, Child's Nervous System.

Adrenal function of extremely premature infants in the first 5 days after birth

M. Turner, M. Didi, S. Ng, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

The diagnosis and treatment of adrenal insufficiency during childhood and adolescence

M. Didi, J. Blair, Julie Park, 2016, Archives of Disease in Childhood.

Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans

G. Kokai, A. Grüters, M. Wlodarski, 2017, The Journal of clinical investigation.

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

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

Disproportionate short stature after cranial irradiation and combination chemotherapy for leukaemia.

A. Ogilvy-Stuart, S. Shalet, J. Wales, 1994, Archives of disease in childhood.

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.

Neonatal Pituitary-Thyroid Axis Dysregulation with Combined Thyroid Hormone and Thyrotropin Resistance in Infant with Trisomy 21 and Maternal Subclinical Hypothyroidism

M. Didi, A. Soni, S. Ng, 2017 .

The role of surgery in optic pathway/hypothalamic gliomas in children.

J. Blair, B. Pizer, C. Mallucci, 2014, Journal of neurosurgery. Pediatrics.

An explanatory randomised placebo controlled trial of levothyroxine supplementation for babies born <28 weeks’ gestation: results of the TIPIT trial

C. Gamble, Richa Gupta, S. Victor, 2013, Trials.

TIPIT: A randomised controlled trial of thyroxine in preterm infants under 28 weeks' gestation

C. Gamble, S. Victor, M. Turner, 2008, Trials.

Clinical and morphological characteristics of ectopic thyroid gland in children: A series of 24 patients from Northwest India

R. Prasad, K. Sodhi, A. Bhattacharya, 2017 .

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

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

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

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

Adrenal responses to a low‐dose short synacthen test in children with asthma

M. Pirmohamed, R. Smyth, A. Jorgensen, 2016, Clinical endocrinology.

Skin microvascular reactivity in children and adolescents with type 1 diabetes in relation to levels of physical activity and aerobic fitness.

G. Stratton, S. Edmunds, M. Didi, 2008, Pediatric exercise science.

Study protocol for a randomised controlled trial of insulin delivery by continuous subcutaneous infusion compared to multiple daily injections

C. Gamble, D. Hughes, C. Ridyard, 2015, Trials.

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.

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.

Continuous subcutaneous insulin infusion versus multiple daily injections in children and young people at diagnosis of type 1 diabetes: the SCIPI RCT.

C. Gamble, D. Hughes, C. Ridyard, 2018, Health technology assessment.

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

P. Clayton, L. Patel, I. Banerjee, 2013, Front. Endocrinol..

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.

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.

The role of early intra-operative MRI in partial resection of optic pathway/hypothalamic gliomas in children

E. Lewis, M. Spiteri, C. Mallucci, 2015, Child's Nervous System.

Pubertal growth in young adult survivors of childhood leukemia.

S. Shalet, J. Wales, H. Davies, 1995, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Continuous subcutaneous insulin infusion versus multiple daily injection regimens in children and young people at diagnosis of type 1 diabetes: pragmatic randomised controlled trial and economic evaluation

C. Gamble, D. Hughes, C. Ridyard, 2019, BMJ.

Cranial MRI scans are indicated in all girls with central precocious puberty

M. Didi, S. Ng, C. S. Smith, 2003, Archives of disease in childhood.

Adrenal responses to a low‐dose short synacthen test in children with asthma

M. Pirmohamed, A. Jorgensen, P. Newland, 2015, Clinical endocrinology.