E-LIB Suche - Ergebnisse für: Finckh, U

1

Cancer spectrum and frequency among children with Noonan, C..:

Kratz, C P ; Franke, L ; Peters, H...
British Journal of Cancer. 112 (2015) 8 - p. 1392-1397 , 2015

Link: https://doi.org/10.1038/..

2

Floating‐Harbor syndrome: SRCAP mutations are not restricte..:

Kehrer, M. ; Beckmann, A. ; Wyduba, J....
Clinical Genetics. 85 (2013) 5 - p. 498-499 , 2013

Link: https://doi.org/10.1111/..

3

Variegate porphyria in a 46‐year‐old patient taking sibutra..:

Reiser, M. ; Eickmann, S. ; Haverkamp, T..
Obesity Reviews. 11 (2010) 4 - p. 329-331 , 2010

Link: https://doi.org/10.1111/..

4

466Correlation of gene expression and genetic alterations i..:

Friedrich, M.G. ; Kuschel, C. ; Kommerau, M....
European Urology Supplements. 4 (2005) 3 - p. 119 , 2005

Link: https://doi.org/10.1016/..

5

Indication of circadian oscillations in the rat pancreas:

Mühlbauer, E ; Wolgast, S ; Finckh, U..
FEBS Letters. 564 (2004) 1-2 - p. 91-96 , 2004

Link: https://doi.org/10.1016/..

6

SH-SY5Y CELLS ARE A MODEL TO STUDY DOPAMINE D2 RECEPTOR (DR..:

Wernicke, C ; Finckh, U ; Rommelspacher, H
Alcoholism: Clinical & Experimental Research. 28 (2004) Supplement - p. 37A , 2004

Link: https://doi.org/10.1097/..

7

Charcot-Marie-Tooth-Erkrankung mit disseminierter Encephalo..:

Lewerenz, J ; Finckh, U ; Ding, X...
Aktuelle Neurologie. 31 (2004) S 1 - p. , 2004

Link: https://doi.org/10.1055/..

8

The future of genetic association studies in Alzheimer dise..:

Finckh, U.
Journal of Neural Transmission. 110 (2003) 3 - p. 253-266 , 2003

Link: https://doi.org/10.1007/..

9

CSF-tau, CSF-A�1-42, ApoE-genotype and clinical parameters ..:

Ganzer, S. ; Arlt, S. ; Schoder, V....
Journal of Neural Transmission. 110 (2003) 10 - p. 1149-1160 , 2003

Link: https://doi.org/10.1007/..

10

Association of late-onset Alzheimer disease with a genotype..:

Finckh, U. ; van Hadeln, K. ; Müller-Thomsen, T....
Neurogenetics. 4 (2003) 4 - p. 213-217 , 2003

Link: https://doi.org/10.1007/..

11

Variable expression of familial Alzheimer disease associate..:

Finckh, U. ; Alberici, A. ; Antoniazzi, M....
Neurology. 54 (2000) 10 - p. 2006-2008 , 2000

Link: https://doi.org/10.1212/..

12

Genetic association of an ( 2-macroglobulin (Val1000lle) po..:

Liao, A. ; Nitsch, R. M. ; Greenberg, S. M....
Human Molecular Genetics. 7 (1998) 12 - p. 1953-1956 , 1998

Link: https://doi.org/10.1093/..

13

Absence of angiotensin II type 1 receptor gene mutations in..:

Sachse, R ; Shao, XJ ; Rico, A...
European Journal of Endocrinology. , 1997

Link: https://doi.org/10.1530/..

14

Absence of human T-lymphotrophic virus type I in patients w..:

LIPKA, K. ; TEBBE, B. ; FINCKH, U..
Clinical and Experimental Dermatology. 21 (1996) 1 - p. 38-42 , 1996

Link: https://doi.org/10.1111/..

15

Absence of human T-lymphotrophic virus type I in patients w..:

LIPKA, K. ; TEBBE, B. ; FINCKH, U..
Clinical and Experimental Dermatology. 21 (1996) 1 - p. 38-42 , 1996

Link: https://doi.org/10.1046/..