Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Jakob Høgild, Langdahl"'
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Akademický článek
Mitochondrial mutation m.3243A>G associates with insulin resistance in non-diabetic carriers
Autor: Jakob Høgild Langdahl, Anja Lisbeth Frederiksen, John Vissing, Morten Frost, Knud Bonnet Yderstræde, Per Heden Andersen
Publikováno v: Endocrine Connections, Vol 8, Iss 7, Pp 829-837 (2019)
Aim: This case–control study aimed to examine impairments in glucose metabolism in non-diabetic carriers of the mitochondrial mutation m.3243A>G by evaluating insulin secretion capacity and sensitivity. Methods: Glucose metabolism was investigated
Externí odkaz: https://doaj.org/article/59d1205e113740a8a2a33594ac121aba
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2
Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10-year Prospective Cohort
Autor: Knud Bonnet Yderstræde, Mads Thomassen, Anja Lisbeth Frederiksen, Per Heden Andersen, Morten Duno, John Vissing, Jakob Høgild Langdahl, Martin Jakob Larsen, Morten Frost
Publikováno v: Langdahl, J H, Larsen, M, Frost, M, Andersen, P H, Yderstraede, K B, Vissing, J, Dunø, M, Thomassen, M & Frederiksen, A L 2018, ' Lecocytes mutation load declines with age in carriers of the m.3243A >G mutation : A 10-year Prospective Cohort ', Clinical Genetics, vol. 93, no. 4, pp. 925-928 . https://doi.org/10.1111/cge.13201
Carriers of the mitochondrial mutation m.3243A>G presents highly variable phenotypes including mitochondrial encephalomyopathy, lactoacidosis and stroke-like episodes (MELAS). We conducted a follow-up study to evaluate changes in leucocyte heteroplas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::922f5232e0e3e5509448c10136fb462a
https://doi.org/10.1111/cge.13201
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3
Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study
Autor: Knud Bonnet Yderstræde, Jakob Høgild Langdahl, Stinus Hansen, Anja Lisbeth Frederiksen, Morten Duno, Per Heden Andersen, Morten Frost, John Vissing
Publikováno v: Journal of Bone and Mineral Research. 32:2041-2048
Mitochondrial dysfunction is associated with several clinical manifestations including diabetes, neurological disorders, renal and hepatic diseases and myopathy. While mitochondrial dysfunction is associated with increased bone resorption and decreas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::db392219f4f14aafc01c326c384d747d
https://doi.org/10.1002/jbmr.3193
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4
Mitochondrial mutation m.3243A>G associates with insulin resistance in non-diabetic carriers
Autor: Anja Lisbeth Frederiksen, Knud Bonnet Yderstræde, John Vissing, Jakob Høgild Langdahl, Per Heden Andersen, Morten Frost
Publikováno v: Langdahl, J H, Frederiksen, A L, Vissing, J, Frost, M, Yderstræde, K B & Andersen, P H 2019, ' Mitochondrial mutation m.3243A >G associates with insulin resistance in non-diabetic carriers. ', Endocrine Connections, vol. 8, no. 7, pp. 829–837 . https://doi.org/10.1530/EC-19-0118
Endocrine Connections
Langdahl, J H, Frederiksen, A L, Vissing, J, Frost, M, Yderstræde, K B & Andersen, P H 2019, ' Mitochondrial mutation m.3243A >G associates with insulin resistance in non-diabetic carriers ', Endocrine Connections, vol. 8, no. 7, pp. 829-837 . https://doi.org/10.1530/EC-19-0118
Endocrine Connections, Vol 8, Iss 7, Pp 829-837 (2019)
Aim This case–control study aimed to examine impairments in glucose metabolism in non-diabetic carriers of the mitochondrial mutation m.3243A>G by evaluating insulin secretion capacity and sensitivity. Methods Glucose metabolism was investigated in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f085afd825eade5ddbe87322553c5fe9
https://findresearcher.sdu.dk:8443/ws/files/151612210/_20493614_Endocrine_Connections_Mitochondrial_mutation_m.3243A_gt_G_associates_with_insulin_resistance_in_non_diabetic_carriers.pdf
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6
Mitochondrial Point Mutation m.3243AG Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study
Autor: Jakob Høgild, Langdahl, Anja Lisbeth, Frederiksen, Stinus Jørn, Hansen, Per Heden, Andersen, Knud Bonnet, Yderstraede, Morten, Dunø, John, Vissing, Morten, Frost
Publikováno v: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 32(10)
Mitochondrial dysfunction is associated with several clinical manifestations including diabetes mellitus (DM), neurological disorders, renal and hepatic diseases, and myopathy. Although mitochondrial dysfunction is associated with increased bone reso
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2ba4aeee677882187da8561c83643b17
https://pubmed.ncbi.nlm.nih.gov/28850729
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7
Boucher Neuhäuser Syndrome - A rare cause of inherited hypogonadotropic hypogonadism. A case of two adult siblings with two novel mutations in PNPLA6
Autor: Jakob Høgild Langdahl, Claus B. Juhl, Nina N. T. T. Nguyen, Anja Lisbeth Frederiksen, Klaus Brusgaard
Publikováno v: Langdahl, J H, Frederiksen, A L, Nguyen, N N T T, Brusgaard, K & Juhl, C B 2017, ' Boucher Neuhäuser Syndrome-A rare cause of inherited hypogonadotropic hypogonadism : A case of two adult siblings with two novel mutations in PNPLA6 ', European Journal of Medical Genetics, vol. 60, no. 2, pp. 105-109 . https://doi.org/10.1016/j.ejmg.2016.11.003
Boucher Neuhäuser Syndrome (BNS) is a rare clinical syndrome with autosomal recessive inheritance defined by early-onset ataxia, hypogonadism and chorioretinal dystrophy. We present two siblings diagnosed with BNS in late adult life identified with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db89c73c39c791be408cb7d922c7b3f3
https://pubmed.ncbi.nlm.nih.gov/27866050
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