Friederike Burger
Overview
Explore the profile of Friederike Burger including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
188
Followers
0
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Recent Articles
1.
Stich M, Magalhaes V, Burger F, Garbade S, Jeltsch K, Mohr K, et al.
J Med Virol
. 2024 Dec;
96(12):e70098.
PMID: 39624009
The pivotal role of the cell entry receptor ACE2 for SARS-CoV-2 infection is well-established. When ACE2 is shed from cell surface into plasma as soluble ACE2 (sACE2), it can effectively...
2.
Laugwitz L, Mechtler T, Janzen N, Oliva P, Kasper A, Teunissen C, et al.
N Engl J Med
. 2024 Sep;
391(13):1256-1258.
PMID: 39292923
No abstract available.
3.
Himmelreich N, Kikul F, Zdrazilova L, Honzik T, Hecker A, Poschet G, et al.
Mol Genet Metab
. 2023 May;
139(3):107610.
PMID: 37245379
PMM2-CDG is the most common defect among the congenital disorders of glycosylation. In order to investigate the effect of hypoglycosylation on important cellular pathways, we performed extensive biochemical studies on...
4.
Burger F, Koch M, Fraatz M, Omarini A, Berger R, Zorn H
Molecules
. 2022 Feb;
27(3).
PMID: 35163915
The production of natural flavors by means of microorganisms is of great interest for the food and flavor industry, and by-products of the agro-industry are particularly suitable as substrates. In...
5.
Beck-Wodl S, Kehrer C, Harzer K, Haack T, Burger F, Haas D, et al.
JIMD Rep
. 2021 Mar;
58(1):80-88.
PMID: 33728250
Multiple sulfatase deficiency (MSD) is a lysosomal storage disease caused by a deficiency of formylglycine-generating enzyme due to defects. MSD may be misdiagnosed as metachromatic leukodystrophy (MLD), as neurological and...
6.
Navolan D, Stoian D, Bohiltea R, Crainiceanu Z, Craina M, Cretu O, et al.
Exp Ther Med
. 2020 Aug;
20(3):2449-2454.
PMID: 32765732
Inflammatory mechanisms are involved in achieving a normal pregnancy and in the development of certain pregnancy complications. These changes are more intense in pregnant women that suffer of pregnancy complications,...
7.
Meyburg J, Opladen T, Spiekerkotter U, Schlune A, Schenk J, Schmidt J, et al.
J Inherit Metab Dis
. 2017 Oct;
41(1):81-90.
PMID: 29027067
Background: Urea cycle disorders (UCDs) still have a poor prognosis despite several therapeutic advancements. As liver transplantation can provide a cure, liver cell therapy (LCT) might be a new therapeutic...
8.
Mutze U, Burger F, Hoffmann J, Tegetmeyer H, Heichel J, Nickel P, et al.
Mol Genet Metab Rep
. 2016 Dec;
10:1-4.
PMID: 27942463
Background: Lysosomal storage diseases (LSD) often manifest with cherry red macular spots. Diagnosis is based on clinical features and specific biochemical and enzymatic patterns. In uncertain cases, genetic testing with...
9.
Stockklausner C, Raffel S, Klermund J, Bandapalli O, Beier F, Brummendorf T, et al.
Aging (Albany NY)
. 2015 Nov;
7(11):911-27.
PMID: 26546739
The TERT gene encodes for the reverse transcriptase activity of the telomerase complex and mutations in TERT can lead to dysfunctional telomerase activity resulting in diseases such as dyskeratosis congenita...
10.
Kastner B, Behre S, Lutz N, Burger F, Luntz S, Hinderhofer K, et al.
PLoS One
. 2015 Aug;
10(8):e0135997.
PMID: 26275228
Background: Children and patients with cognitive deficits may find it difficult to understand the implication of research. In the European Union (EU), clinical studies outside the EU directives concerning medicinal...