Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Karen E. Cosgrove"'
Autor:
Ross J. Craigie, Maria Salomon-Estebanez, Daphne Yau, Bing Han, Walaa Mal, Melanie Newbould, Edmund Cheesman, Stefania Bitetti, Zainab Mohamed, Rakesh Sajjan, Raja Padidela, Mars Skae, Sarah Flanagan, Sian Ellard, Karen E. Cosgrove, Indraneel Banerjee, Mark J. Dunne
Publikováno v:
Frontiers in Endocrinology, Vol 9 (2018)
Background: Congenital Hyperinsulinism (CHI) is an important cause of severe and persistent hypoglycaemia in infancy and childhood. The focal form (CHI-F) of CHI can be potentially cured by pancreatic lesionectomy. While diagnostic characteristics of
Externí odkaz:
https://doaj.org/article/5c2269549a354e929fa1fb91b08c9b12
Autor:
Indraneel Banerjee, Chris Worth, Senthil Senniappan, Karen E Cosgrove, Yesica Tropeano, Pon Ramya Gokul, Maria Salomon-Estebanez, Antonia Dastamani
Publikováno v:
BMJ Open Diabetes Research & Care, Vol 10, Iss 3 (2022)
Externí odkaz:
https://doaj.org/article/7c354fef92714b9bbfe3bbf53b8cbbbe
Autor:
Chris Worth, Laila Al Hashmi, Daphne Yau, Maria Salomon-Estebanez, Diego Perez Ruiz, Caroline Hall, Elaine O’Shea, Helen Stokes, Peter Foster, Sarah E. Flanagan, Karen E Cosgrove, Mark J Dunne, Indraneel Banerjee
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Hypoglycaemia due to hyperinsulinism (HI) is the commonest cause of severe, recurrent hypoglycaemia in childhood. Cohort outcomes of HI remain to be described and whilst previous follow up studies have focused on neurodevelopmenta
Externí odkaz:
https://doaj.org/article/c9c9cf55681d4829a4cbd4c89e2b61d0
Autor:
Sophie G Kellaway, Karolina Mosinska, Zainaba Mohamed, Alexander Ryan, Stephen Richardson, Melanie Newbould, Indraneel Banerjee, Mark J Dunne, Karen E Cosgrove
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0223999 (2019)
[This corrects the article DOI: 10.1371/journal.pone.0222350.].
Externí odkaz:
https://doaj.org/article/462d6d03ce0941a8914ea06fd78fc76f
Autor:
Sophie G Kellaway, Karolina Mosinska, Zainaba Mohamed, Alexander Ryan, Stephen Richardson, Melanie Newbould, Indraneel Banerjee, Mark J Dunne, Karen E Cosgrove
Publikováno v:
PLoS ONE, Vol 14, Iss 9, p e0222350 (2019)
Congenital hyperinsulinism (CHI) is characterised by inappropriate insulin secretion causing profound hypoglycaemia and brain damage if inadequately controlled. Pancreatic tissue isolated from patients with diffuse CHI shows abnormal proliferation ra
Externí odkaz:
https://doaj.org/article/ac9e4dea76914cc4b864d4487b65b226
Autor:
Chris Worth, Yesica Tropeano, Pon Ramya Gokul, Karen E Cosgrove, Maria Salomon-Estebanez, Senthil Senniappan, Antonia Dastamani, Indraneel Banerjee
Publikováno v:
Worth, C, Tropeano, Y, Gokul, P R, Cosgrove, K E, Salomon-Estebanez, M, Senniappan, S, Dastamani, A & Banerjee, I 2022, ' Insight into hypoglycemia frequency in congenital hyperinsulinism: evaluation of a large UK CGM dataset ', BMJ open diabetes research & care, vol. 10, no. 3, e002849 . https://doi.org/10.1136/bmjdrc-2022-002849
IntroductionHypoglycemia is often recurrent and severe in patients with congenital hyperinsulinism (CHI). However, there is little information regarding frequency or patterns of episodes to inform clinical management and future trial design.Research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ea820e6770e0e75d4a82b1db2f32b55
https://pubmed.ncbi.nlm.nih.gov/35675953
https://pubmed.ncbi.nlm.nih.gov/35675953
Autor:
Indraneel (Indi) eBanerjee, Lynette eForsythe, Mars eSkae, Hima Bindu Avatapalle, Lindsey eRigby, Louise E Bowden, Ross eCraigie, Raja ePadidela, Sarah eEhtisham, Leena ePatel, Karen E Cosgrove, Mark eDunne, Peter eClayton
Publikováno v:
Frontiers in Endocrinology, Vol 7 (2016)
Background: Congenital Hyperinsulinism (CHI) is a rare but severe disorder of hypoglycaemia in children, often complicated by brain injury. In CHI, the long term prevention of hypoglycaemia is dependent on reliable enteral intake of glucose. However,
Externí odkaz:
https://doaj.org/article/9c315e68b1c146c1ace4b3deb1e15c05
Autor:
Elaine O’Shea, Indraneel Banerjee, Karen E. Cosgrove, Helen Stokes, Daphne Yau, Diego Andres Perez Ruiz, Maria Salomon-Estebanez, Chris Worth, Laila Al Hashmi, Sarah E. Flanagan, Mark J. Dunne, Caroline Hall, Peter William Foster
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Hypoglycaemia due to hyperinsulinism (HI) is the commonest cause of severe, recurrent hypoglycaemia in childhood. Cohort outcomes of HI remain to be described and whilst previous follow up studies have focused on neurodevelopmental outcome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac20fe5d13b00b57d761fbe31a66d085
http://link.springer.com/article/10.1186/s13023-020-01438-0
http://link.springer.com/article/10.1186/s13023-020-01438-0
Autor:
Chris Worth, Karen E. Cosgrove, Elaine O’Shea, Daphne Yau, Maria Salomon Estebanez, Indraneel Banerjee, Mark J. Dunne
Publikováno v:
Worth, C, Yau, D, Salomon Estebanez, M, O’shea, E, Cosgrove, K, Dunne, M & Banerjee, I 2020, ' Complexities in the medical management of hypoglycaemia due to congenital hyperinsulinism ', Clinical Endocrinology . https://doi.org/10.1111/cen.14152, https://doi.org/10.1111/cen.14152
Congenital Hyperinsulinism (CHI) is a rare disease of hypoglycaemia but is the most common form of recurrent and severe hypoglycaemia causing brain injury and neurodisability in children. The management of CHI is complex due to the limited choice of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c400cfb6ed80533d8969eaa4f2ae431
https://doi.org/10.1111/cen.14152
https://doi.org/10.1111/cen.14152
Autor:
Mars eSkae, Hima Bindu eAvatapalle, Indraneel (Indi) eBanerjee, Lindsey eRigby, Andy eVail, Peter eFoster, Christiana eCharalambous, Louise eBowden, Raja ePadidela, Leena ePatel, Sarah eEhtisham, Karen E Cosgrove, Mark eDunne, Peter eClayton
Publikováno v:
Frontiers in Endocrinology, Vol 5 (2014)
Objective: Congenital Hyperinsulinism (CHI) is a rare condition of hypoglycaemia where therapeutic options are limited and often complicated by side-effects. Omega-3-polyunsaturated fatty acids (PUFA) which can suppress cardiac myocyte electrical act
Externí odkaz:
https://doaj.org/article/ea30dd0cafd846db90d5998ef617bd96