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Archived publications before 2003

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The employees at the Medical Care Centre Dr. Eberhard & Partner Dortmund are directly involved in current medical developments through their work. Several of our academic employees are actively involved in medical research and collaborate in scientific studies from hospitals and universities. This commitment to science is expressed in medical publications. The following is a compilation of recent scientific publications.

Zum Archiv (Veröffentlichungen älter als 10 Jahre)

Markus Kostrzewa, Elisabeth Nagy, Percy Schröttner, Arthur B. Pranada

How MALDI-TOF mass spectrometry can aid the diagnosis of hard-to-identify pathogenic bacteria - the rare and the unknown
in: Expert Review of Molecular Diagnostics, 13. July 2019

Miriam Cordovana, Arthur B. Pranada, Simone Ambretti, Markus Kostrzewa

MALDI-TOF bacterial subtyping to detect antibiotic resistance,
in: Clinical Mass Spectrometry, 14 June 2019.

Miriam Cordovana, Markus Kostrzewa, Jörg Glandorf, Michael Bienia, Simone Ambretti and Arthur B. Pranada

A Full MALDI-Based Approach to Detect Plasmid-Encoded KPC-Producing Klebsiella pneumoniae,
in: Frontiers in Microbiology, 23. November 2018.

Wünsche, Falko

Hyponatriämie - Natrium und Wasser im Ungleichgewicht
Pharmazeutische Zeitung, 162 (49), 34-41 (2017)

Wünsche, Falko

Transfusionsmedizin - Blutprodukte unter strenger Kontrolle
Pharmazeutische Zeitung, 162 (34), 20-27 (2017)

Tsagoudis K, Magiera-Lappann I, Haverkamp T, Drebber U, Agaimy A, Tantcheva-Poόr I.

Hereditary leiomyomatosis and renal cell cancer syndrome: A novel mutation in the FH gene.
J Dermatol. 2017 Jul 10. doi: 10.1111/1346-8138.13955.

Strotmann, Falko

Schnelltests – Was der Urin verrät
Pharmazeutische Zeitung, 162 (15), 40-47 (2017)

Strotmann, Falko

Nebennieren: Über-, Unter- und Fehlfunktionen
Pharmazeutische Zeitung, 160 (16), 27-35 (2015)

Falko Strotmann, Corinna Nöcker, Nicole Crummenerl, Bianca Karnuth, Nilma Kamp, Gerd Hafner

Inappropriate Blood Transfusion in Neonatal Hemolytic Anemia Due to Anti-c
American Journal of Medical Case Reports
Vol. 5, No. 3, 2017, pp 56-58. doi: 10.12691/ajmcr-5-3-3

Jakob Meinel, Ulrich Finckh, Andreas Schuster, Thomas Haverkamp, Annette Richter-Unruh

Establishment of Clinical and Lab Algorithms for the Identification Carriers of Mutations in CYP21A2 – A Study of 768 Children and Adolescents
European Society for Paediatric Endocrinology, ESPE Abstracts (2016) 86 P-P1-13

Balasubramaniam S, Lewis B, Greed L, Meili D, Flier A, Yamamoto R, Bilić K, Till C, Sass JO.

Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent Ketoacidosis.
JIMD Rep. 2015 Nov 26.

Petrides PE, Stölzl U, Stauch T, Kehl F, Haverkamp T, Frank J,

Die akuten Porphyrien. Eine Informationsbroschüre für Ärzte. 2015. 4. Auflage. 1. Auflage Dietzenbach 2008.

Kämpfe D., Haverkamp T., Schulte B., Ganster C., Haase D.

CALR mutations in cMPN. Experience with 185 patients of the Single Center Register (SCR) Lüdenscheid.
Oncol Res Treat 2014;37(suppl 5):314–331.

Anne Schänzer, Christoph Kimmich, Christoph Röcken, Thomas Haverkamp, Isabell Weidner, Till Acker, Heidrun H Krämer

A woman with a rare p.Glu74Gly transthyretin mutation presenting exclusively with a rapidly progressive neuropathy: a case report

Journal of Medical Case Reports 2014, 8:403 (4 December 2014)
Abstract online

Strotmann, Falko

Klinische Chemie - Laborbefunde kritisch beurteilen
Pharmazeutische Zeitung, 159 (44), 28-35 (2014)

Zum Archiv (Veröffentlichungen älter als 10 Jahre)