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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)

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, Front. Microbiol., 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)

DL Kämpfe, J. Friemann, T. Haverkamp, S. Killburger, B. Schulte, HL Pahl

Cyclic thrombocytosis in a patient with PV resolved by ruxolitinib treatment

HAEMATOLOGICA / 19th congress Mailand 2014, ABSTRACT BOOK, abstract PB1749

Luedecke D, Becktepe JS, Lehmbeck J, Finckh U, Yamamoto R, Jahn H, Boelmans K.

A novel presenilin 1 mutation (Ala275Val) as cause of early-onset familial Alzheimer disease

Neurosci Lett 566:115-119, 2014. Im Internet bei PubMed NCBI.

Zum Archiv (Veröffentlichungen älter als 10 Jahre)