Zobrazeno 1 - 10
of 40
pro vyhledávání: '"idiopathic ketotic hypoglycemia"'
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 3, Pp 152-155 (2024)
Idiopathic ketotic hypoglycemia (IKH) is defined as bouts of hypoglycemia with increased blood or urine ketones in certain children after prolonged fasting or during illness. IKH is divided into physiological IKH, which is most frequently observed in
Externí odkaz:
https://doaj.org/article/664302bd49f646cbbe2a951f0d43ce66
Akademický článek
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Autor:
Danielle Drachmann, Erica Hoffmann, Austin Carrigg, Beccie Davis-Yates, Valerie Weaver, Paul Thornton, David A. Weinstein, Jacob S. Petersen, Pratik Shah, Henrik Thybo Christesen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Background Idiopathic Ketotic hypoglycemia (IKH) is a diagnosis of exclusion. Although considered as the most frequent cause of hypoglycemia in childhood, little progress has been made to advance the understanding of IKH since the medical te
Externí odkaz:
https://doaj.org/article/49e270f85bb449af8057226d59dae7fd
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Pediatric Epilepsy. :048-050
Idiopathic ketotic hypoglycemia (IKH) is characterized by recurrent neurohypoglycemic symptoms with ketosis. Hypoglycemic episodes typically occur during early mornings, especially either with illness and/or prolonged fasting. We reported a case of I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2a3b42c274db4728a225173638830f5
https://doi.org/10.1055/s-0040-1710043
https://doi.org/10.1055/s-0040-1710043
Autor:
Paul B. Kaplowitz, Hilal Sekizkardes
Publikováno v:
International Journal of Pediatric Endocrinology, Vol 2019, Iss 1, Pp 1-7 (2019)
International Journal of Pediatric Endocrinology
International Journal of Pediatric Endocrinology
Introduction Idiopathic ketotic hypoglycemia (KH) is the most common cause of hypoglycemia in non-diabetic children ages 0.5–6 years old and typically occurs after a period of poor food intake. There are no large studies looking at the value of com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beeddc3db3b406ab6be74dbe4414f8ed
http://link.springer.com/article/10.1186/s13633-019-0066-9
http://link.springer.com/article/10.1186/s13633-019-0066-9
Autor:
Anja Lisbeth Frederiksen, Diva D. De León, Matthew Lines, Henrik Thybo Christesen, Anne Benner, Yazeid Alhaidan, Klaus Brusgaard, Rebecca Sparkes
Publikováno v:
American Journal of Medical Genetics. Part a
Benner, A, Alhaidan, Y, Lines, M A, Brusgaard, K, De Leon, D D, Sparkes, R, Frederiksen, A L & Christesen, H T 2021, ' PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only ', American Journal of Medical Genetics. Part A, vol. 185, no. 10, pp. 2959-2975 . https://doi.org/10.1002/ajmg.a.62383
Benner, A, Alhaidan, Y, Lines, M A, Brusgaard, K, De Leon, D D, Sparkes, R, Frederiksen, A L & Christesen, H T 2021, ' PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only ', American Journal of Medical Genetics, Part A, vol. 185, no. 10, pp. 2959-2975 . https://doi.org/10.1002/ajmg.a.62383
Benner, A, Alhaidan, Y, Lines, M A, Brusgaard, K, De Leon, D D, Sparkes, R, Frederiksen, A L & Christesen, H T 2021, ' PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only ', American Journal of Medical Genetics. Part A, vol. 185, no. 10, pp. 2959-2975 . https://doi.org/10.1002/ajmg.a.62383
Benner, A, Alhaidan, Y, Lines, M A, Brusgaard, K, De Leon, D D, Sparkes, R, Frederiksen, A L & Christesen, H T 2021, ' PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only ', American Journal of Medical Genetics, Part A, vol. 185, no. 10, pp. 2959-2975 . https://doi.org/10.1002/ajmg.a.62383
Idiopathic ketotic hypoglycemia (IKH) is a diagnosis of exclusion with glycogen storage diseases (GSDs) as a differential diagnosis. GSD IXa presents with ketotic hypoglycemia (KH), hepatomegaly, and growth retardation due to PHKA2 variants. In our m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ab32b34e290997f431eff4eecb45ff8
https://pubmed.ncbi.nlm.nih.gov/34117828
https://pubmed.ncbi.nlm.nih.gov/34117828
Publikováno v:
Frontiers in Endocrinology
Frontiers in Endocrinology, Vol 11 (2021)
Siersbæk, J, Larsen, A R, Nybo, M & Christesen, H T 2021, ' A Sensitive Plasma Insulin Immunoassay to Establish the Diagnosis of Congenital Hyperinsulinism ', Frontiers in Endocrinology, vol. 11, 614993 . https://doi.org/10.3389/fendo.2020.614993
Frontiers in Endocrinology, Vol 11 (2021)
Siersbæk, J, Larsen, A R, Nybo, M & Christesen, H T 2021, ' A Sensitive Plasma Insulin Immunoassay to Establish the Diagnosis of Congenital Hyperinsulinism ', Frontiers in Endocrinology, vol. 11, 614993 . https://doi.org/10.3389/fendo.2020.614993
BackgroundThe diagnosis of congenital hyperinsulinism (CHI) may be hampered by a plasma (p-) insulin detection limit of 12–18 pmol/L (2–3 mU/L).ObjectiveTo evaluate the diagnostic performance of a sensitive insulin immunoassay and to find the opt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdade355a771ac2572329815ecda928e
https://doi.org/10.3389/fendo.2020.614993
https://doi.org/10.3389/fendo.2020.614993
Akademický článek
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