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The Journal of Biological Chemistry|April 13, 2011
Daxx-beta and Daxx-gamma, two novel splice variants of the transcriptional co-repressor DaxxNils Wethkamp, Helmut Hanenberg, Sarah Funke, et al.
Frontiers in Neurology|April 7, 2022
Impact of COVID-19 Pandemic on Treatment Management and Clinical Outcome of Aneurysmal Subarachnoid Hemorrhage - A Single-Center ExperienceSepide Kashefiolasl, Lina Elisabeth Qasem, Nina Brawanski, et al.
Human Molecular Genetics|June 17, 1999
A common molecular basis for rearrangement disorders on chromosome 22q11L Edelmann, R K Pandita, E Spiteri, et al.
Atherosclerosis|February 10, 1997
Heterozygous hepatic lipase deficiency, due to two missense mutations R186H and L334F, in the HL geneP Knudsen, M Antikainen, M Uusi-Oukari, et al.
Nutrition (Burbank, Los Angeles County, Calif.)|March 12, 2014
Bone mineral density, vitamin D, and nutritional status of children submitted to hematopoietic stem cell transplantationDenise Johnsson Campos, César Luiz Boguszewski, Vaneuza Araujo Moreira Funke, et al.
BMC Public Health|September 19, 2024
Patients' and stakeholders' experiences of a personalized self-management SUPport program (P-SUP) for patients with type 2 diabetes mellitus and/or coronary heart disease: a qualitative process evaluation : Maximilian SchollMaximilian Scholl, Jessica Amerkamp, Chloé Chermette, et al.
Plos One|October 5, 2018
Human immunodeficiency virus status in malnourished children seen at LagosEdamisan Olusoji Temiye, Oluwafunmilayo Funke Adeniyi, Iretiola Bamikeolu Fajolu, et al.
BMC Infectious Diseases|October 3, 2023
Circulating calprotectin levels four months after severe and non-severe COVID-19N Abu Hussein, C Machahua, S C Ruchti, et al.
Plos One|February 4, 2016
Competitive Mirror Image Phage Display Derived Peptide Modulates Amyloid Beta Aggregation and ToxicityStephan Rudolph, Antonia Nicole Klein, Markus Tusche, et al.
The Journal of Clinical Investigation|February 1, 1993
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this diseaseH Funke, A von Eckardstein, P H Pritchard, et al.
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