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Nadja Baumgartner

Observed names: Baumgartner, Nadja, N Baumgartner, N. Baumgartner
OpenAlex ID: A5047040602
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea
2015 · Andreas R. Janecke, Peter Heinz-Erian, et al. · Human Molecular Genetics · 135
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Increased Serum Lipoprotein(a) Concentrations and Low Molecular Weight Phenotypes of Apolipoprotein(a) Are Associated with Symptomatic Peripheral Arterial Disease
2007 · Benjamin Dieplinger, Arno Lingenhel, et al. · Clinical Chemistry · 71
Lipocalin‐2 ensures host defense against Salmonella Typhimurium by controlling macrophage iron homeostasis and immune response
2015 · Manfred Nairz, Andrea Schroll, et al. · European Journal of Immunology · 67
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Impact of D181V and A69T on the function of ferroportin as an iron export pump and hepcidin receptor
2014 · Roman Praschberger, Melanie Schranz, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 24
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Synonymous mutation in adenosine triphosphatase copper‐transporting beta causes enhanced exon skipping in Wilson disease
2022 · Marlene Panzer, André Viveiros, et al. · Hepatology Communications · 16
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Reduced iron export associated with hepcidin resistance can explain the iron overload spectrum in ferroportin disease
2020 · André Viveiros, Marlene Panzer, et al. · Liver International · 16
The RS855791 polymorphism of TMPRSS6 is not a genetic modifier of hereditary hemochromatosis
2012 · R Mayr, N Baumgartner, et al. · Zeitschrift für Gastroenterologie · 3
HFE Genotypen, Eisenstatus und Überleben
2014 · A Finkenstedt, M Schranz, et al. · Zeitschrift für Gastroenterologie · 1
Weniger ist oft mehr
2026 · Baumgartner, Nadja · Universitätsbibliothek Tübingen - Open Journals - Heiliger Dienst: Vierteljahresschrift
International Evaluation of the Aquaporin-4 Antibody Rapid Idot Test (LS1.005)
2026 · Margherita Vacca, Rui Li, et al. · Neurology
Autosomal Dominant Familial Intestinal Varicosis and Polyposis coli is associated with Pathogenic Variants in NKX2.3
2021 · M Grossgut, B Schaefer, et al. · Zeitschrift für Gastroenterologie
The Phenotypic Spectrum of Patients with Genetic variants in Ceruloplasmin
2021 · E Pertler, M Panzer, et al. · Zeitschrift für Gastroenterologie
A cellular disease model for autosomal dominant ferroportin gene mutations
2019 · M Panzer, A Viveiros, et al. · Zeitschrift für Gastroenterologie
Ferroportin Mutation oder benigner Sequenz Polymorphismus?
2012 · M Schranz, R Mayr, et al. · Zeitschrift für Gastroenterologie
1390 the Rs855791 Polymorphism of Tmprss6 Is Not a Genetic Modifier of Hereditary Hemochromatosis
2012 · R. Mayr, N. Baumgartner, et al. · Journal of Hepatology
Works count: 15
Citation count: 333
H-index: 6
I10-index: 6
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