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Results: 1-16 |
Results: 16
Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes
Authors: Schneider, C Wessig, C Muller, CR Brechtelsbauer, D Grimm, T
Citation: C. Schneider et al., Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes, NEUROMUSC D, 11(5), 2001, pp. 485-488
Nikolaus Friedreich, the first Heidelberg neurologist
Authors: Grimm, T
Citation: T. Grimm, Nikolaus Friedreich, the first Heidelberg neurologist, F NEUR PSYC, 69, 2001, pp. S8-S10
Genomic organization and embryonic expression of Suppressor of Fused, a candidate gene for the split-hand/split-foot malformation type 3
Authors: Grimm, T Teglund, S Tackels, D Sangiorgi, E Gurrieri, F Schwartz, C Toftgard, R
Citation: T. Grimm et al., Genomic organization and embryonic expression of Suppressor of Fused, a candidate gene for the split-hand/split-foot malformation type 3, FEBS LETTER, 505(1), 2001, pp. 13-17
Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration
Authors: Sauer, CG White, K Stohr, H Grimm, T Hutchinson, A Bernstein, PS Lewis, RA Simonelli, F Pauleikhoff, D Allikmets, R Weber, BHF
Citation: Cg. Sauer et al., Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration, BR J OPHTH, 85(8), 2001, pp. 969-975
Simultaneous interdisciplinary counseling in German breast/ovarian cancer families: First experiences with patient perceptions, surveillance behaviorand acceptance of genetic testing
Authors: Hofferbert, S Worringen, U Backe, J Ruckert, EM White, K Faller, H Grimm, T Caffier, H Chang-Claude, J Weber, BHF
Citation: S. Hofferbert et al., Simultaneous interdisciplinary counseling in German breast/ovarian cancer families: First experiences with patient perceptions, surveillance behaviorand acceptance of genetic testing, GEN COUNSEL, 11(2), 2000, pp. 127-146
Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2)
Authors: Kress, W Mueller-Myhsok, B Ricker, K Schneider, C Koch, MC Toyka, KV Mueller, CR Grimm, T
Citation: W. Kress et al., Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2), NEUROMUSC D, 10(7), 2000, pp. 478-480
Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM)
Authors: Schneider, C Grimm, T Kress, W Sommer, C Muller, CR
Citation: C. Schneider et al., Hyperparathyroidism in a patient with proximal myotonic myopathy (PROMM), NEUROMUSC D, 10(7), 2000, pp. 481-483
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly
Authors: Kress, W Petersen, B Collmann, H Grimm, T
Citation: W. Kress et al., An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly, CYTOG C GEN, 91(1-4), 2000, pp. 138-140
Proximal myotonic myopathy - Evidence for anticipation in families with linkage to chromosome 3q
Authors: Schneider, C Ziegler, A Ricker, K Grimm, T Kress, W Reimers, CD Meinck, HM Reiners, K Toyka, KV
Citation: C. Schneider et al., Proximal myotonic myopathy - Evidence for anticipation in families with linkage to chromosome 3q, NEUROLOGY, 55(3), 2000, pp. 383-388
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration
Authors: Rivera, A White, K Stohr, H Steiner, K Hemmrich, N Grimm, T Jurklies, B Lorenz, B Scholl, HPN Apfelstedt-Sylla, E Weber, BHF
Citation: A. Rivera et al., A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration, AM J HU GEN, 67(4), 2000, pp. 800-813
Mammalian Suppressor-of-Fused modulates nuclear-cytoplasmic shuttling of GLI-1
Authors: Kogerman, P Grimm, T Kogerman, L Krause, D Unden, AB Sandstedt, B Toftgard, R Zaphiropoulos, PG
Citation: P. Kogerman et al., Mammalian Suppressor-of-Fused modulates nuclear-cytoplasmic shuttling of GLI-1, NAT CELL BI, 1(5), 1999, pp. 312-319
Linkage analysis and genetic models in dyslexia - considerations pertaining to discrete trait analysis and quantitative trait analyses
Authors: Muller-Myhsok, B Grimm, T
Citation: B. Muller-myhsok et T. Grimm, Linkage analysis and genetic models in dyslexia - considerations pertaining to discrete trait analysis and quantitative trait analyses, EUR CHILD A, 8, 1999, pp. 40-42
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15
Authors: Nothen, MM Schulte-Korne, G Grimm, T Cichon, S Vogt, IR Muller-Myhsok, B Propping, P Remschmidt, H
Citation: Mm. Nothen et al., Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15, EUR CHILD A, 8, 1999, pp. 56-59
Interleukin-1 haplotype and periodontal disease progression following therapy
Authors: Ehmke, B Kress, W Karch, H Grimm, T Klaiber, B Flemmig, TF
Citation: B. Ehmke et al., Interleukin-1 haplotype and periodontal disease progression following therapy, J CLIN PER, 26(12), 1999, pp. 810-813
Linkage of proximal myotonic myopathy to chromosome 3q
Authors: Ricker, K Grimm, T Koch, MC Schneider, C Kress, W Reimers, CD Schulte-Mattler, W Mueller-Myhsok, B Toyka, KV Mueller, CR
Citation: K. Ricker et al., Linkage of proximal myotonic myopathy to chromosome 3q, NEUROLOGY, 52(1), 1999, pp. 170-171
Buoyancy-driven mean flow in a long channel with a hydraulically constrained exit condition
Authors: Grimm, T Maxworthy, T
Citation: T. Grimm et T. Maxworthy, Buoyancy-driven mean flow in a long channel with a hydraulically constrained exit condition, J FLUID MEC, 398, 1999, pp. 155-180
Risultati: 1-16 |