Zobrazeno 1 - 10 of 75 pro vyhledávání: '"Ritika R Kapoor"'
1
Akademický článek
Pituitary apoplexy in an adolescent male with macroprolactinoma presenting as middle cerebral artery territory infarction
Autor: Pankaj Agrawal, Sally Newbold, Ayisha Al Busaidi, Ritika R Kapoor, Nick Thomas, Simon JB Aylwin, Charles R Buchanan, Ved Bhushan Arya
Publikováno v: Annals of Pediatric Endocrinology & Metabolism, Vol 27, Iss 4, Pp 320-324 (2022)
Pituitary apoplexy typically presents with acute headache, vomiting, visual disturbance, and confusion. Herein, we report a rare presentation of ischemic stroke due to pituitary apoplexy. A 16.5-year-old male presented with reduced Glasgow Coma Scale
Externí odkaz: https://doaj.org/article/05bedfee044c402e985317309df508d9
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2
Akademický článek
Central Diabetes Insipidus in Children and Adolescents: Twenty-Six Year Experience from a Single Centre
Autor: Hüseyin Anil Korkmaz, Ritika R Kapoor, Jennifer Kalitsi, Simon JB Aylwin, Charles R Buchanan, Ved Bhushan Arya
Publikováno v: International Journal of Endocrinology, Vol 2022 (2022)
Introduction. Paediatric cohorts of central diabetes insipidus (CDI) have shown varying prevalence for different causes of CDI. The objective of this study was to determine the causes of CDI and long-term outcome in children and adolescents from a Te
Externí odkaz: https://doaj.org/article/330eaf96cd3a4ea7977d2bb243df405b
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3
Akademický článek
Exceptional diazoxide sensitivity in hyperinsulinaemic hypoglycaemia due to a novel HNF4A mutation
Autor: Ved Bhushan Arya, Jennifer Kalitsi, Ann Hickey, Sarah E Flanagan, Ritika R Kapoor
Publikováno v: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2019)
Diazoxide is the first-line treatment for patients with hyperinsulinaemic hypoglycaemia (HH). Approximately 50% of patients with HH are diazoxide resistant. However, marked diazoxide sensitivity resulting in severe hyperglycaemia is extremely uncom
Externí odkaz: https://doaj.org/article/7d9b332bb89c4cbca06c5d7fee711aa6
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4
Akademický článek
Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389.
Autor: Daphne Yau, Thomas W Laver, Antonia Dastamani, Senthil Senniappan, Jayne A L Houghton, Guftar Shaikh, Tim Cheetham, Talat Mushtaq, Ritika R Kapoor, Tabitha Randell, Sian Ellard, Pratik Shah, Indraneel Banerjee, Sarah E Flanagan
Publikováno v: PLoS ONE, Vol 15, Iss 2, p e0228417 (2020)
Congenital hyperinsulinism (CHI) is a significant cause of hypoglycaemia in neonates and infants with the potential for permanent neurologic injury. Accurate calculations of the incidence of rare diseases such as CHI are important as they inform heal
Externí odkaz: https://doaj.org/article/bcf7bd9b0a414b47a5a19639403cea32
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5
Akademický článek
Paternal uniparental isodisomy of chromosome 11p15.5 within the pancreas causes isolated hyperinsulinaemic hypoglycaemia
Autor: Sarah E Flanagan, Ritika R Kapoor, Virpi V. Smith, Khalid eHussain, Sian eEllard
Publikováno v: Frontiers in Endocrinology, Vol 2 (2011)
BackgroundLoss of function mutations in the genes encoding the pancreatic β-cell ATP-sensitive potassium (KATP) channel are identified in approximately 80% of patients with diazoxide-unresponsive hyperinsulinaemic-hypoglycaemia (HH). For a small num
Externí odkaz: https://doaj.org/article/3158ae4c327d4754867c5dcbf2dbfa18
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8
Prolactinoma in childhood and adolescence—Tumour size at presentation predicts management strategy: Single centre series and a systematic review and meta‐analysis
Autor: Nicholas Thomas, Tim Hampton, Tony Hulse, Istvan Bodi, Charles Buchanan, Ved Bhushan Arya, Ritika R Kapoor, Michal Ajzensztejn, Simon Aylwin, Jennifer Kalitsi, Nicolas Kalogirou
Publikováno v: Clinical Endocrinology. 94:413-423
To report the clinical presentation, management and outcomes of young patients with prolactinomas (20 years) and conduct a systematic review and meta-analysis.Clinical, biochemical and radiological data (1996-2018) were collected from our centre. A s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::145c99540109421f8af2641846eb5a47
https://doi.org/10.1111/cen.14394
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9
IgG4-related hypophysitis in adolescence
Autor: Ritika R. Kapoor, David D'Cruz, Tim Hampton, Zita Reisz, Charles R. Buchanan, Sreena Das, Ved Bhushan Arya, Andy King, Bassel Zebian, Sarra Abu El-Gasim, Simon Aylwin
Publikováno v: Journal of Pediatric Endocrinology and Metabolism. 34:395-399
Objectives IgG4-related hypophysitis is a novel clinical disease entity, which is typically seen in the sixth decade of life and is typically complicated by hypopituitarism. We describe an adolescent female with IgG4-related hypophysitis with normal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1883250b7ef1b0e25b8863bcfaa96c69
https://doi.org/10.1515/jpem-2020-0535
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10
Hyperinsulinemic hypoglycemia in children and adolescents: Recent advances in understanding of pathophysiology and management
Autor: Ritika R. Kapoor, Sofia Rahman, Sarah E. Flanagan, Nick Oliver, Pratik Shah, Maria Gϋemes, Mehul T. Dattani, Jayne A L Houghton, Shivani Misra
Publikováno v: Reviews in Endocrine & Metabolic Disorders
Hyperinsulinemic hypoglycemia (HH) is characterized by unregulated insulin release, leading to persistently low blood glucose concentrations with lack of alternative fuels, which increases the risk of neurological damage in these patients. It is the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::303722f42756f9bba61ca4f55147b44d
https://doi.org/10.1007/s11154-020-09548-7
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