November 2015
Autor(en): 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.
Publiziert: JIMD Rep. 2015 Nov 26.
Februar 2015
Autor(en): Kerstin Maria Kampa-Schittenhelm, MD , Hans-Joerg Buehring , Michael Bonin , Wichard Vogel, MD , Lothar Kanz, Prof. Dr. MD , Thomas Haverkamp , Marcus M Schittenhelm, MD
Epigenetic Upregulation of the O-Linked Beta-N-Acetylglucosamine Transferase (OGT) in Response to Dronabinol Results in Antileukemic Efficacy In Vivo
Publiziert: Blood (2015) 126 (23): 2437
Dezember 2014
Autor(en): 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
Publiziert: Journal of Medical Case Reports 2014, 8:403 (4 December 2014)
Publiziert: Pharmazeutische Zeitung, 159 (44), 28-35 (2014)
September 2014
Autor(en): 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.
Publiziert: Oncol Res Treat 2014;37(suppl 5):314331.
Februar 2014
Autor(en): 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
Publiziert: Neurosci Lett 566:115-119, 2014. Im Internet bei PubMed NCBI.
Januar 2014
Autor(en): DL Kämpfe, J. Friemann, T. Haverkamp, S. Killburger, B. Schulte, HL Pahl
Cyclic thrombocytosis in a patient with PV resolved by ruxolitinib treatment
Publiziert: HAEMATOLOGICA / 19th congress Mailand 2014, ABSTRACT BOOK, abstract PB1749
September 2013
Autor(en): Kehrmann A, Truong H, Repenning A, Boger R, Klein-Hitpass L, Pascheberg U, Beckmann A, Opalka B, Kleine-Lowinski K
Complementation of non-tumorigenicity of HPV18-positive cervical carcinoma cells involves differential mRNA expression of cellular genes including potential tumor suppressor genes on chromosome 11q13
Publiziert: Cancer Genet. 2013 Jul-Aug;206(7-8):279-92. doi: 10.1016/j.cancergen.2013.06.002. Epub 2013 Sep 14.
Juni 2013
Autor(en): Kehrer M, Beckmann A, Wyduba J, Finckh U, Dufke A, Gaiser U, Tzschach A
Floating-Harbor syndrome: SRCAP mutations are not restricted to exon 34
Publiziert: Clin Genet. 2013 Jun 13. doi: 10.1111/cge.12199
Januar 2013
Autor(en): C.L. Behnes, C. Schlegel, M. Shoukier, I. Magiera, F. Henschke, A. Schwarz, F. Bremmer, H. Loertzer
Hereditary papillary renal cell carcinoma primarily diagnosed in a cervical lymph node: a case report of a 30-year-old woman with multiple metastases.
Publiziert: BMC Urology 2013, 13:3 doi:10.1186/1471-2490-13-3 Der Artikel ist online abrufbar unter biomedcentral.