Jacqueline Nicholson
Overview
Explore the profile of Jacqueline Nicholson including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
99
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0
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Recent Articles
1.
Shaikh M, Lucas-Herald A, Dastamani A, Estebanez M, Senniappan S, Abid N, et al.
Front Endocrinol (Lausanne)
. 2023 Nov;
14:1231043.
PMID: 38027197
Congenital hyperinsulinism (CHI) is a condition characterised by severe and recurrent hypoglycaemia in infants and young children caused by inappropriate insulin over-secretion. CHI is of heterogeneous aetiology with a significant...
2.
Stokes H, Jones J, Worth C, Nicholson J, Fullwood C, Banerjee I
Front Endocrinol (Lausanne)
. 2023 Jun;
14:1167854.
PMID: 37324260
Introduction: Easypod-connect™ for childhood growth disorders is a unique connected system that enables transmission of injection adherence information for recombinant human growth hormone (r-hGH). Although this system has the potential...
3.
Chinoy A, Nicholson J, Skae M, Hannan F, Thakker R, Mughal M, et al.
J Pediatr
. 2023 Mar;
257:113367.
PMID: 36868303
Objectives: To evaluate the prevalence and degree of any neurodevelopmental abnormalities in children with familial hypocalciuric hypercalcemia type 3 (FHH3). Study Design: A formal neurodevelopmental assessment was performed in children...
4.
Hennayake S, Barnes A, Mariotto A, Goyal A, Ajao A, Cserni T, et al.
J Pediatr Urol
. 2022 Aug;
18(5):611.e1-611.e8.
PMID: 35970739
In Manchester, feminising genitoplasty is offered to children with 46XX Congenital Adrenal Hyperplasia (CAH) when there is a single perineal opening and/or enlarged clitoris. Our aims are to describe the...
5.
Auckburally S, Worth C, Salomon-Estebanez M, Nicholson J, Harper S, Nutter P, et al.
Front Endocrinol (Lausanne)
. 2022 Aug;
13:894559.
PMID: 35928891
Background And Aims: In patients with congenital hyperinsulinism (CHI), recurrent hypoglycaemia can lead to longstanding neurological impairments. At present, glycaemic monitoring is with intermittent fingerprick blood glucose testing but this...
6.
Salomon-Estebanez M, Mohamed Z, Michaelidou M, Collins H, Rigby L, Skae M, et al.
Orphanet J Rare Dis
. 2017 May;
12(1):96.
PMID: 28532504
Background: Congenital Hyperinsulinism (CHI) is a disease of severe hypoglycaemia caused by excess insulin secretion and associated with adverse neurodevelopment in a third of children. The Vineland Adaptive Behavior Scales...
7.
Salomon-Estebanez M, Flanagan S, Ellard S, Rigby L, Bowden L, Mohamed Z, et al.
Orphanet J Rare Dis
. 2016 Dec;
11(1):163.
PMID: 27908292
Background: Patients with Congenital Hyperinsulinism (CHI) due to mutations in K-ATP channel genes (K-ATP CHI) are increasingly treated by conservative medical therapy without pancreatic surgery. However, the natural history of...
8.
Avatapalle H, Banerjee I, Shah S, Pryce M, Nicholson J, Rigby L, et al.
Front Endocrinol (Lausanne)
. 2013 Jun;
4:60.
PMID: 23730298
Introduction: Neuroglycopenia is recognized to be associated with abnormal neurodevelopmental outcomes in 26-44% of children with persistent congenital hyperinsulinism (P-CHI). The prevalence of abnormal neurodevelopment in transient CHI (T-CHI) is...