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BMJ Case Reports|March 26, 2018
Thyrotoxic crisis as an acute clinical presentation in a childAdam Bonfield, Savitha Shenoy
Acta Paediatrica (Oslo, Norway : 1992)|February 28, 2023
Challenges in using fractional excretion of sodium in the assessment of salt poisoningSavitha Shenoy, Detlef Bockenhauer
Bulletin of Medical Ethics|February 27, 2004
Current practice for obtaining consent in UK neonatal unitsSavitha Shenoy, Carmel Archdeacon, Sailesh Kotecha, et al.
The Pediatric Infectious Disease Journal|July 13, 2018
Comparing the Clinical Severity of Disease Caused by Enteroviruses and Human Parechoviruses in Neonates and InfantsSally Black, Carina Bradley, Florence Y Lai, et al.
Journal of the Indian Society of Pedodontics and Preventive Dentistry|March 17, 2020
Assessing the behavior management problems during the first dental visit of preschool children using a doll placement testAkhil Suresh, Y M Karuna, Srikant Natarajan, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|September 3, 2016
Cluster of human parechovirus infections as the predominant cause of sepsis in neonates and infants, Leicester, United Kingdom, 8 May to 2 August 2016Julian W Tang, Christopher W Holmes, Fadwa A Elsanousi, et al.
Journal of Medical Genetics|October 26, 2010
Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type IbStéphanie Maupetit-Méhouas, Virginie Mariot, Christelle Reynès, et al.
Archives of Disease in Childhood|April 12, 2023
Emergency and perioperative management of adrenal insufficiency in children and young people: British Society for Paediatric Endocrinology and Diabetes consensus guidanceTalat Mushtaq, Salma R Ali, Nabil Boulos, et al.
European Journal of Endocrinology|September 15, 2021
The broad phenotypic spectrum of 17α-hydroxylase/17,20-lyase (CYP17A1) deficiency: a case seriesMin Sun, Jonathan W Mueller, Lorna C Gilligan, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
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