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Results: 1-15 |
Results: 15
Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke
Authors: Lopaciuk, S Bykowska, K Kwiecinski, H Mickielewicz, A Czlonkowska, A Mendel, T Kuczynska-Zardzewialy, A Szelagowska, D Windyga, J Schroder, W Herrmann, FH Jedrzejowska, H
Citation: S. Lopaciuk et al., Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke, CL APPL T-H, 7(4), 2001, pp. 346-350
Influence of the dopamine D-2 receptor (DRD2) exon 8 genotype on efficacy of tiapride and clinical outcome of alcohol withdrawal
Authors: Lucht, MJ Kuehn, KU Schroeder, W Armbruster, J Abraham, G Schattenberg, A Gaensicke, M Barnow, S Tretzel, H Herrmann, FH Freyberger, HJ
Citation: Mj. Lucht et al., Influence of the dopamine D-2 receptor (DRD2) exon 8 genotype on efficacy of tiapride and clinical outcome of alcohol withdrawal, PHARMACOGEN, 11(8), 2001, pp. 647-653
High prevalence of FVHR2 polymorphism in Costarician Indians who have no FVL
Authors: Herrmann, FH Salazar-Sanchez, L Jimenez-Arce, G Grimm, R Schroder, W
Citation: Fh. Herrmann et al., High prevalence of FVHR2 polymorphism in Costarician Indians who have no FVL, THROMB HAEM, 85(6), 2001, pp. 1120-1121
Relationships between homocysteine, folate and vitamin B12 levels with themethylenetetrahydrofolate reductase polymorphism, in Indians from western Venezuela
Authors: Vizcaino, G Diez-Ewald, M Herrmann, FH Schuster, G Perez-Requejo, JL
Citation: G. Vizcaino et al., Relationships between homocysteine, folate and vitamin B12 levels with themethylenetetrahydrofolate reductase polymorphism, in Indians from western Venezuela, THROMB HAEM, 85(1), 2001, pp. 186-187
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data
Authors: Ivaskevicius, V Jurgutis, R Rost, S Muller, A Schmitt, C Wulff, K Herrmann, FH Muller, CR Schwaab, R Oldenburg, J
Citation: V. Ivaskevicius et al., Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data, BR J HAEM, 112(4), 2001, pp. 1062-1070
Factor VIII gene polymorphisms in the Asian Indian population
Authors: Chowdhury, MR Herrmann, FH Schroder, W Lambert, CT Lalloz, MRA Layton, M Kumbnani, HK Kabra, M Menon, PSN Verma, IC
Citation: Mr. Chowdhury et al., Factor VIII gene polymorphisms in the Asian Indian population, HAEMOPHILIA, 6(6), 2000, pp. 625-630
Twenty two novel mutations of the factor VII gene in factor VII deficiency
Authors: Wulff, K Herrmann, FH
Citation: K. Wulff et Fh. Herrmann, Twenty two novel mutations of the factor VII gene in factor VII deficiency, HUM MUTAT, 15(6), 2000, pp. 489-496
First hints for a correlation between amplification of the Int-2 gene and infection with human papillomavirus in head and neck squamous cell carcinomas
Authors: Kleist, B Poetsch, M Bankau, A Werner, E Herrmann, FH Lorenz, G
Citation: B. Kleist et al., First hints for a correlation between amplification of the Int-2 gene and infection with human papillomavirus in head and neck squamous cell carcinomas, J ORAL PATH, 29(9), 2000, pp. 432-437
Molecular biology and clinical manifestation of hereditary factor VII deficiency
Authors: Herrmann, FH Wulff, K Auberger, K Aumann, V Bergmann, F Bergmann, K Bratanoff, E Franke, D Grundeis, M Kreuz, W Lenk, H Losonczy, H Maak, B Marx, G Mauz-Korholz, C Pollmann, H Serban, M Sutor, A Syrbe, G Vogel, G Weinstock, N Wenzel, E Wolf, K
Citation: Fh. Herrmann et al., Molecular biology and clinical manifestation of hereditary factor VII deficiency, SEM THROMB, 26(4), 2000, pp. 393-400
Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7)
Authors: Mariani, G Herrmann, FH Bernardi, F Schved, JF Auerswald, G Ingerslev, J
Citation: G. Mariani et al., Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7), BLOOD, 96(1), 2000, pp. 374-374
Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy
Authors: Hoeltzenbein, M Karow, T Zeller, JA Warzok, R Wulff, K Zschiesche, M Herrmann, FH Grosse-Heitmeyer, W Wehnert, MS
Citation: M. Hoeltzenbein et al., Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy, NEUROMUSC D, 9(3), 1999, pp. 166-170
Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma: FISH deletion screening with YAC DNA probes
Authors: Poetsch, M Woenckhaus, C Dittberner, T Pambor, M Lorenz, G Herrmann, FH
Citation: M. Poetsch et al., Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma: FISH deletion screening with YAC DNA probes, VIRCHOWS AR, 435(2), 1999, pp. 105-111
Different numerical chromosomal aberrations detected by FISH in oropharyngeal, hypopharyngeal and laryngeal squamous cell carcinoma
Authors: Poetsch, M Kleist, B Lorenz, G Herrmann, FH
Citation: M. Poetsch et al., Different numerical chromosomal aberrations detected by FISH in oropharyngeal, hypopharyngeal and laryngeal squamous cell carcinoma, HISTOPATHOL, 34(3), 1999, pp. 234-240
Factor XII deficiency, APC-resistance, hyperhomocysteinemia and von Willebrand's disease type 1 in the same family
Authors: Maak, B Wulff, K Herrmann, FH Schroder, W Budde, U Siegemund, A Ruhling, H
Citation: B. Maak et al., Factor XII deficiency, APC-resistance, hyperhomocysteinemia and von Willebrand's disease type 1 in the same family, MONATS KIND, 147(2), 1999, pp. 104-109
Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene
Authors: Wulff, K Bykowska, K Lopaciuk, S Herrmann, FH
Citation: K. Wulff et al., Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene, ACT BIOCH P, 46(3), 1999, pp. 721-726
Risultati: 1-15 |