Amish Chinoy
Overview
Explore the profile of Amish Chinoy including associated specialties, affiliations and a list of published articles.
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13
Citations
127
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Recent Articles
1.
Nayak S, Rayner L, Mughal Z, McKinney G, Mason A, Wong S, et al.
Arch Dis Child
. 2024 May;
109(10):849-853.
PMID: 38821713
Introduction: Zoledronic acid (ZA), used for treatment of children with osteoporosis, can cause acute phase reaction (APR) following the first infusion. Many institutions have a policy to admit and monitor...
2.
Levene I, Dhami A, Moreno M, Shine B, Chinoy A, Padidela R, et al.
J Paediatr Child Health
. 2023 Aug;
59(10):1140-1145.
PMID: 37545420
Aim: To characterise parathyroid hormone (PTH) concentrations in infants at high risk for metabolic bone disease, in order to assist clinical decisions around the use of PTH for screening. Methods:...
3.
4.
Chinoy A, Padidela R
Indian J Pediatr
. 2023 Apr;
90(6):574-581.
PMID: 37074534
Nutritional rickets, caused by vitamin D and/or calcium deficiency is by far the most common cause of rickets. In resource-limited settings, it is therefore not uncommon to treat rickets with...
5.
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...
6.
Chinoy A, Vassallo G, Burkitt Wright E, Eelloo J, West S, Hupton E, et al.
J Musculoskelet Neuronal Interact
. 2022 Mar;
22(1):70-78.
PMID: 35234161
Neurofibromatosis type 1 (NF1) can affect multiple systems in the body. An under recognised phenotype is one of muscle weakness. Clinical studies using dynamometry and jumping mechanography have demonstrated that...
7.
Normal Mid-Gestation Fetal Ultrasonography Cannot Reliably Exclude Severe Perinatal Hypophosphatasia
Chinoy A, Iruloh C, Kerr B, Mughal M, Padidela R
Horm Res Paediatr
. 2021 Aug;
94(7-8):307-312.
PMID: 34438404
Introduction: Hypophosphatasia is a systemic bone disease characterized by inhibition of bone mineralization due to mutations in the ALPL gene that results in a deficiency of tissue nonspecific alkaline phosphatase....
8.
Chinoy A, Mughal M, Padidela R
Acta Paediatr
. 2020 Nov;
110(6):1855-1862.
PMID: 33145793
Aim: This study aimed to identify current trends in the management of metabolic bone disease of prematurity (MBDP) in the United Kingdom. Methods: A nationwide electronic survey was disseminated to...
9.
Chinoy A, Mughal M, Padidela R
Semin Fetal Neonatal Med
. 2019 Dec;
25(1):101075.
PMID: 31879202
Neonatal care has significantly improved in the past decade with improved survival of preterm and sick neonates. Similarly, the field of bone and mineral disorders is continuing to accelerate with...
10.
Yau D, Salomon-Estebanez M, Chinoy A, Grainger J, Craigie R, Padidela R, et al.
Endocrinol Diabetes Metab Case Rep
. 2019 Aug;
2019(1).
PMID: 31373474
Summary: Congenital hyperinsulinism (CHI) is an important cause of severe hypoglycaemia in infancy. To correct hypoglycaemia, high concentrations of dextrose are often required through a central venous catheter (CVC) with...