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Nisha Nathwani

Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)
2014 · Rathi Prasad, Li F. Chan, et al. · The Journal of Clinical Endocrinology & Metabolism · 142
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Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ
2016 · Adeline K. Nicholas, Eva G. Serra, et al. · The Journal of Clinical Endocrinology & Metabolism · 116
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Primate-specific ZNF808 is essential for pancreatic development in humans
2023 · Elisa De Franco, Nick D. L. Owens, et al. · Nature Genetics · 49
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Antibody Responses to Immunizations in Children with Type I Diabetes Mellitus: a Case-Control Study
2016 · Michael Eisenhut, Alexander Chesover, et al. · Clinical and Vaccine Immunology · 15
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Exploring barriers to expanding medical training numbers in England: A national survey of medical education directors
2025 · Michael Batavanis, Anmol Arora, et al. · Clinical Medicine · 6
Investigating the genetic architecture of gland-in-situ congenital hypothyroidism by comprehensive screening of eight known causative genes
2015 · Adeline K Nicholas, Eva Goncalves Serra, et al. · Endocrine Abstracts · 2
Optimising wound care in a child with an infected gastrostomy exit site
2013 · Hazel Rollins, Nisha Nathwani, et al. · British Journal of Nursing · 2
A mutation in thioredoxin reductase 2 is associated with familial glucocorticoid deficiency
2013 · Rathi Prasad, Li F. Chan, et al. · 1
A mutation in thioredoxin reductase 2 (TXNRD2) is associated with a predominantly adrenal phenotype in humans
2013 · Rathi Prasad, Claire Hughes, et al. · Endocrine Abstracts · 1
Transient Broca's Aphasia as Feature of an Extradural Abscess
2008 · Raghuram Commondoor, Michael Eisenhut, et al. · Pediatric Neurology · 1
Iatrogenic adrenal suppression in children: how 'stressed' should paediatricians be?
2025 · Eleanor Crawley, Claire Westcott, et al. · Endocrine Abstracts
Addressing Health Inequalities – Creating Educational Supervision Capacity
2023 · Jack Haywood, Adrian Brooke, et al.
Hypercalcaemia as a presenting feature of sarcoidosis: the need for an open mind
2019 · Meera Mallya, Usha Niranjan, et al. · Endocrine Abstracts
G385(P) A safety revolution: cross-speciality engagement of junior doctors in patient safety
2018 · BP Marlow, N Nathwani
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G157(P) Antibody responses to immunizations in children with type i diabetes mellitus: A case-control study
2017 · M Eisenhut, A Chesover, et al.
An incidental finding of an abdominopelvic macrocystic lymphangioma in a girl with Turners syndrome
2015 · Jasjit Kaur Bhandari, Nisha Nathwani · Endocrine Abstracts
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Obesity: a diagnostic dilemma
2015 · Jasjit Kaur Bhandari, Stalin Ramprakash, et al. · Endocrine Abstracts
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G302(P) Obesity – why do clinicians still turn a “blind eye”
2015 · L Ek, T Waterfield, et al. · Archives of Disease in Childhood
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G22(P) Use of blood gas and blood ketones in management of children with gastroenteritis
2014 · J. Palman, R. Misquith, et al. · Archives of Disease in Childhood
Diabetes transitional care in a district general hospital: an audit
2012 · R Misquith, N Nathwani, et al. · Archives of Disease in Childhood
The usefulness of vitamin D measurements in a busy General Paediatric Unit
2011 · Santhosh Olety Sathyanarayana, Nisha Nathwani, et al. · British Society for Paediatric Endocrinology and Diabetes Meeting (BSPED)
Spectrum of Inherited Metabolic Disorders Presenting in the Newborn Period in a District General Hospital
2008 · Pritesh Munot, Anusha Arasu, et al. · Archives of Disease in Childhood
Adolescent endocrinology; time to revisit the diagnoses? a case of septo-optic dysplasia
2007 · Rajeev Kumar, Nisha Nathwani, et al. · Society for Endocrinology BES
Works count: 23
Citation count: 335
H-index: 5
I10-index: 4
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