Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Elisa Waldmann"'
Autor:
Viktoria F Koehler, Patrick Keller, Elisa Waldmann, Nathalie Schwenk, Carolin Kitzberger, Kathrin A Schmohl, Thomas Knösel, Christian Georg Stief, Christine Spitzweg
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2021)
Introduction: Struma ovarii is a teratoma of the ovaries predominantly composed of thyroid tissue. Hyperthyroidism associated with struma ovarii is rare, occurring in approximately 8% of cases. Due to the rarity of struma ovarii, available data are l
Externí odkaz:
https://doaj.org/article/b89858bb7bdf44049d99817ccc3d5cfa
Autor:
Elisa Waldmann, Liya Wu, Kristina Busygina, Julia Altenhofer, Kerstin Henze, Alexander Folwaczny, Klaus G. Parhofer
Publikováno v:
PLoS ONE, Vol 17, Iss 3 (2022)
Background and aims Familial dysbetalipoproteinemia (FDBL) is a rare inborn lipid disorder characterized by the formation of abnormal triglyceride- and cholesterol-rich lipoproteins (remnant particles). Patients with FDBL have a high risk for atheros
Externí odkaz:
https://doaj.org/article/360f58bffc12493b9f84ab21bee50732
Autor:
Elisa Waldmann, Klaus G. Parhofer
Publikováno v:
Journal of Lipid Research, Vol 57, Iss 10, Pp 1751-1757 (2016)
An elevated plasma concentration of lipoprotein (a) [Lp(a)] is an independent risk factor for cardiovascular disease. Life style modification and currently available drugs either fail to effectively lower plasma Lp(a) levels or do not result in clini
Externí odkaz:
https://doaj.org/article/c811e0ef0a4b4fdb9ad288219be51e3b
Autor:
Elisa Waldmann
Publikováno v:
MMW - Fortschritte der Medizin. 162:38-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a3b1adc5b748d7ce3fb4bb2720a2cbe
https://doi.org/10.1007/s15006-020-0427-6
https://doi.org/10.1007/s15006-020-0427-6
Publikováno v:
Molecular Genetics and Metabolism. 129:59-66
Background Lysosomal acid lipase (LAL) deficiency is an ultra-rare, progressive, autosomal recessive disorder. Functional mutations in LIPA, the gene that encodes LAL, result in accumulation of cholesteryl esters and triglycerides in hepatocytes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c89a604ba4b9d9cff5886754a2f9fa1
https://doi.org/10.1016/j.ymgme.2019.11.004
https://doi.org/10.1016/j.ymgme.2019.11.004
Autor:
Elisa Waldmann, Liya Wu, Kristina Busygina, Julia Altenhofer, Kerstin Henze, Alexander Folwaczny, Klaus G. Parhofer
Publikováno v:
PloS one. 17(3)
Background and aims Familial dysbetalipoproteinemia (FDBL) is a rare inborn lipid disorder characterized by the formation of abnormal triglyceride- and cholesterol-rich lipoproteins (remnant particles). Patients with FDBL have a high risk for atheros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5af85a12cbe50993ccb8aae03cc74563
https://pubmed.ncbi.nlm.nih.gov/35320320
https://pubmed.ncbi.nlm.nih.gov/35320320
Autor:
Elisa Waldmann
Publikováno v:
MMW - Fortschritte der Medizin. 161:51-54
Der 55-jahrige Herr F. O. wird zur Lebertransplantation stationar aufgenommen. Eine Glukosestoffwechselstorung ist bei ihm nicht vorbekannt. Zwei Wochen nach der Transplantation erhalt der Patient eine Immunsuppression mit Prednisolon 20 mg 1−0−0
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e3fa7b74881d213c590ea68c114b3e2
https://doi.org/10.1007/s15006-019-0513-9
https://doi.org/10.1007/s15006-019-0513-9
Publikováno v:
Nutrients
Volume 13
Issue 5
Nutrients, Vol 13, Iss 1737, p 1737 (2021)
Volume 13
Issue 5
Nutrients, Vol 13, Iss 1737, p 1737 (2021)
Fasting and postprandial hypertriglyceridemia are causal risk factors for atherosclerosis. The prevalence of hypertriglyceridemia is approximately 25–30% and most hypertriglyceridemic patients suffer from mild to moderate hypertriglyceridemia. Data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59a29ff58f3fe0e9d0a76d6f09748cca
https://pubmed.ncbi.nlm.nih.gov/34065380
https://pubmed.ncbi.nlm.nih.gov/34065380
Autor:
Carolin Kitzberger, Viktoria Florentine Koehler, Nathalie Schwenk, Elisa Waldmann, Thomas Knösel, Christine Spitzweg, Kathrin A Schmohl, Christian G. Stief, Patrick Keller
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2021)
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2021)
Summary Struma ovarii is a teratoma of the ovaries predominantly composed of thyroid tissue. Hyperthyroidism associated with struma ovarii is rare, occurring in approximately 8% of cases. Due to the rarity of struma ovarii, available data are limited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa8420c59666b480d2d4c6f09df72887
https://pubmed.ncbi.nlm.nih.gov/33682680
https://pubmed.ncbi.nlm.nih.gov/33682680
Publikováno v:
Digestive diseases (Basel, Switzerland). 39(4)
Objective: Although obesity is associated with metabolic changes, not all obese patients are characterized by the metabolic syndrome (MS). The goal of this study was to determine the prevalence of the MS, its characteristics, and the associated demog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bfd56b20fdcc05db45350b0c65dadb5
https://pubmed.ncbi.nlm.nih.gov/33197923
https://pubmed.ncbi.nlm.nih.gov/33197923