Zobrazeno 1 - 10
of 413
pro vyhledávání: '"J. Müller-Höcker"'
Autor:
J. Stieber, Robert David, Heiko Lickert, Ralph A.W. Rupp, Wolfgang-Michael Franz, Florian Schwarz, S. Kitajima, M. Vollmer, Stefan Brunner, Christoph Brenner, J. Müller-Höcker, Edith Mentele
Publikováno v:
Nature Cell Biology. 10:338-345
ES-cell-based cardiovascular repair requires an in-depth understanding of the molecular mechanisms underlying the differentiation of cardiovascular ES cells. A candidate cardiovascular-fate inducer is the bHLH transcription factor MesP1. As one of th
Publikováno v:
Zeitschrift für Gastroenterologie. 40:885-890
A 26-year-old woman presented with elevated liver enzymes, which were diagnosed two months ago. Examination revealed mild proximal muscle weakness, though the patient herself did not realise any impairment. The abdominal ultrasound and the histology
Autor:
F.J. Tigges, W. Nathrath, R. Hartenstein, B. Anderegg, S. Pachmann, N. Brack, J. Müller-Höcker, Reinhold Munker
Publikováno v:
American Journal of Hematology. 70:167-173
We report the case of a patient with lymphoma of the salivary gland, at first diagnosed as lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) but later found to infiltrate the bone marrow. At diagnosis, the patient had a polyclonal increas
Publikováno v:
Scopus-Elsevier
Regulation of endometrial glucose transport is important for the decidualization process. Therefore, we have examined the expression of the glucose transporter protein isoform 1 (GLUT1) in endometrial samples during the menstrual cycle and in decidua
Autor:
Chuanbing Zang, J. Müller-Höcker, Jan Eucker, Ernest Beutler, P. E. Petrides, H. Harder, Kurt Possinger
Publikováno v:
Annals of Hematology. 79:640-643
We report about a 58-year-old female with coexisting type-I Gaucher's disease (GD) and multiple myeloma (MM). The diagnosis of GD was made in early childhood by means of bone marrow biopsy and was recently confirmed by analysis of the patient's genom
Autor:
Hans Georg Koch, Eberhard Kuwertz-Bröking, Monika Bulla, Erik Harms, Rainer Rossi, Udo Helmchen, J. Müller-Höcker, T. Marquardt
Publikováno v:
Pediatric Nephrology. 14:495-498
A 2-year-old boy who developed hypophosphatemic rickets without signs of muscular weakness or neurological disturbances is presented. Biochemical findings included hypophosphatemia, metabolic acidosis, hypouricemia, hyperphosphaturia, severe glucosur
Publikováno v:
Der Radiologe. 40:475-478
Autor:
J. Müller-Höcker, A. Stäbler, H. Fürst, R. Tiling, Michael M. Ritter, E. Laubach, A. Geier, Peter Schwandt
Publikováno v:
Der Internist. 40:311-315
Eine 60jahrige Patientin mit einem 9 Monate zuvor resezierten Nebenschilddrusen-Karzinom wurde mit Muskelschwache, Polyurie, Polydipsie und unstillbarem Erbrechen in somnolentem Zustand stationar aufgenommen. Bei der klinischen Untersuchung imponiert
Autor:
J. Müller-Höcker
Publikováno v:
Der Pathologe. 19:104-114
Die vorliegende Arbeit gibt eine Ubersicht uber onkozytare Metaplasien- und Neoplasien. Dabei werden insbesondere biochemische, zytochemische und molekulargenetische Ergebnisse erortert. Bekannt ist, das in onkozytaren Zellen der Nebenschilddruse sow
Autor:
Daniel Seehofer, Claus Hammer, Holger Baatz, Joachim Thiery, Jutta Müller-derlich, J. Müller-Höcker
Publikováno v:
Transplantation. 63:460-465
Background. Alterations in microcirculation are considered central to the pathogenesis of hyperacute xenogeneic rejection (HXR) of vascularized xenografts, but currently there exist no data describing these microhemodynamic alterations. Methods. Rat