Eberhard Karls Universität Tübingen

University / College


Location: Tübingen, Germany (DE) DE

ISNI: 0000000121901447

ROR: https://ror.org/03a1kwz48

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Measurement of kidney perfusion by magnetic resonance imaging: Comparison of MRI with arterial spin labeling to para-aminohippuric acid plasma clearance in male subjects with metabolic syndrome (2010) Ritt M, Janka RM, Schneider MP, Martirosian P, Hornegger J, Bautz W, Uder M, Schmieder R Journal article, Original article Discovery of VHE γ -rays from the BL Lacertae object PKS 0548-322 (2010) Aharonian F, Akhperjanian AG, Anton G, De Almeida UB, Bazer-Bachi AR, Becherini Y, Behera B, et al. Journal article, Original article First detection of VHE γ-rays from SN 1006 by HESS (2010) Acero F, Aharonian F, Akhperjanian AG, Anton G, De Almeida UB, Bazer-Bachi AR, Becherini Y, et al. Journal article, Original article Adult neural precursor cells unaffected in animal models of DYT1 dystonia (2009) Regensburger M, Kohl Z, Grundmann K, Winner B, Riess O, Winkler J Journal article Enhancement of dilution and transverse reactive mixing in porous media: Experiments and model-based interpretation (2009) Rolle M, Eberhardt C, Chiogna G, Cirpka OA, Grathwohl P Journal article Updating the orbital ephemeris of Hercules X-1; rate of decay and eccentricity of the orbit (2009) Staubert R, Klochkov D, Wilms J Journal article Red Devonian trilobites with green eyes from Morocco and the silicification of the trilobite exoskeleton (2009) Klug C, Schulz H, de Baets K Journal article, Original article Two similar to 35 day clocks in Hercules X-1: evidence for neutron star free precession (2009) Staubert R, Klochkov D, Postnov K, Shakura N, Wilms J, Rothschild RE Journal article Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization (2009) Bauer P, Winner B, Schüle R, Bauer C, Häfele V, Hehr U, Bonin M, et al. Journal article Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia (2009) Schüle R, Schlipf N, Synofzik M, Klebe S, Klimpe S, Hehr U, Winner B, et al. Journal article