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Results: 1-13 |
Results: 13
Non-replication of association between cathepsin D genotype and late onsetAlzheimer disease
Authors: Menzer, G Muller-Thomsen, T Meins, W Alberici, A Binetti, G Hock, C Nitsch, RM Stoppe, G Reiss, J Finckh, U
Citation: G. Menzer et al., Non-replication of association between cathepsin D genotype and late onsetAlzheimer disease, AM J MED G, 105(2), 2001, pp. 179-182
Ethanol and gene expression in brain
Authors: Matsumoto, I Wilce, PA Buckley, T Dodd, P Puzke, J Spanagel, R Zieglgansberger, W Wolf, G Leng, S Rommelspacher, H Finckh, U Schmidt, LG
Citation: I. Matsumoto et al., Ethanol and gene expression in brain, ALC CLIN EX, 25(5), 2001, pp. 82S-86S
Molecular genetic alterations on chromosomes 11 and 22 in ependymomas
Authors: Lamszus, K Lachenmayer, L Heinemann, U Kluwe, L Finckh, U Hoppner, W Stavrou, D Fillbrandt, R Westphal, M
Citation: K. Lamszus et al., Molecular genetic alterations on chromosomes 11 and 22 in ependymomas, INT J CANC, 91(6), 2001, pp. 803-808
Predominant influence of the 3 '-region of dopamine D-2 receptor gene (DRD2) on the clinical phenotype in German alcoholics
Authors: Samochowiec, J Ladehoff, M Pelz, J Smolka, M Schmidt, LG Rommelspacher, H Finckh, U
Citation: J. Samochowiec et al., Predominant influence of the 3 '-region of dopamine D-2 receptor gene (DRD2) on the clinical phenotype in German alcoholics, PHARMACOGEN, 10(5), 2000, pp. 471-475
Prenatal molecular diagnosis of L1-spectrum disorders
Authors: Finckh, U Gal, A
Citation: U. Finckh et A. Gal, Prenatal molecular diagnosis of L1-spectrum disorders, PRENAT DIAG, 20(9), 2000, pp. 744-745
Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease (vol 92, pg 40, 2000)
Authors: Finckh, U Schroder, J Ressler, B Veske, A Gal, A
Citation: U. Finckh et al., Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease (vol 92, pg 40, 2000), AM J MED G, 94(5), 2000, pp. 438-438
Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease
Authors: Finckh, U Schroder, J Ressler, B Veske, A Gal, A
Citation: U. Finckh et al., Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease, AM J MED G, 92(1), 2000, pp. 40-46
Variable expression of familial Alzheimer disease associated with presenilin 2 mutation M239I
Authors: Finckh, U Alberici, A Antoniazzi, M Benussi, L Fedi, V Giannini, C Gal, A Nitsch, RM Binetti, G
Citation: U. Finckh et al., Variable expression of familial Alzheimer disease associated with presenilin 2 mutation M239I, NEUROLOGY, 54(10), 2000, pp. 2006-2008
Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease
Authors: Finckh, U von der Kammer, H Velden, J Michel, T Andresen, B Deng, A Zhang, J Muller-Thomsen, T Zuchowski, K Menzer, G Mann, U Papassotiropoulos, A Heun, R Zurdel, J Holst, F Benussi, L Stoppe, G Reiss, J Miserez, AR Staehelin, HB Rebeck, GW Hyman, BT Binetti, G Hock, C Growdon, JH Nitsch, RM
Citation: U. Finckh et al., Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease, ARCH NEUROL, 57(11), 2000, pp. 1579-1583
Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia - Reply
Authors: Finckh, U Muller-Thomsen, T Mann, U Eggers, C Marksteiner, J Meins, W Binetti, G Alberici, A Hock, C Nitsch, RM Gal, A
Citation: U. Finckh et al., Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia - Reply, AM J HU GEN, 67(4), 2000, pp. 1035-1036
High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes
Authors: Finckh, U Muller-Thomsen, T Mann, U Eggers, C Marksteiner, J Meins, W Binetti, G Alberici, A Hock, C Nitsch, RM Gal, A
Citation: U. Finckh et al., High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes, AM J HU GEN, 66(1), 2000, pp. 110-117
Lack of an allelic association between polymorphisms of the dopamine D2 receptor gene and alcohol dependence in the German population
Authors: Sander, T Ladehoff, M Samochowiec, J Finckh, U Rommelspacher, H Schmidt, LG
Citation: T. Sander et al., Lack of an allelic association between polymorphisms of the dopamine D2 receptor gene and alcohol dependence in the German population, ALC CLIN EX, 23(4), 1999, pp. 578-581
Simple PCR amplification of the entire glucocerebrosidase gene (GBA) coding region for diagnostic sequence analysis
Authors: Finckh, U Seeman, P von Widdern, OC Rolfs, A
Citation: U. Finckh et al., Simple PCR amplification of the entire glucocerebrosidase gene (GBA) coding region for diagnostic sequence analysis, DNA SEQ, 8(6), 1998, pp. 349-356
Risultati: 1-13 |