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Results: 1-8 |
Results: 8
High prevalence of the H1069Q mutation in East German patients with Wilsondisease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis
Authors: Caca, K Ferenci, P Kuhn, HJ Polli, C Willgerodt, H Kunath, B Hermann, W Mossner, J Berr, F
Citation: K. Caca et al., High prevalence of the H1069Q mutation in East German patients with Wilsondisease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis, J HEPATOL, 35(5), 2001, pp. 575-581
Diagnosis and management of juvenile hyperthyroidism in Germany: A retrospective multicenter study
Authors: Dotsch, J Siebler, T Hauffa, BP Doeker, B Andler, W Bettendorf, M Heinrich, U Gohlke, B Albers, N Willgerodt, H Kiess, W
Citation: J. Dotsch et al., Diagnosis and management of juvenile hyperthyroidism in Germany: A retrospective multicenter study, J PED END M, 13(7), 2000, pp. 879-885
Variable phenotype associated with Ser505Asn-activating thyrotropin-receptor germline mutation
Authors: Fuhrer, D Mix, M Wonerow, P Richter, I Willgerodt, H Paschke, R
Citation: D. Fuhrer et al., Variable phenotype associated with Ser505Asn-activating thyrotropin-receptor germline mutation, THYROID, 9(8), 1999, pp. 757-761
Potential hepatotoxicity of penicillamine treatment in three patients withWilson's disease
Authors: Deutscher, J Kiess, W Scheerschmidt, G Willgerodt, H
Citation: J. Deutscher et al., Potential hepatotoxicity of penicillamine treatment in three patients withWilson's disease, J PED GASTR, 29(5), 1999, pp. 628-628
Urinary excretion of nitrogen containing metabolites of former hypotrophicinfants
Authors: Richter, T Georgi, A Willgerodt, H Muller, DM
Citation: T. Richter et al., Urinary excretion of nitrogen containing metabolites of former hypotrophicinfants, MONATS KIND, 147(10), 1999, pp. 924-926
Linkage of familial euthyroid goiter to the multinodular goiter-1 locus and exclusion of the candidate genes thyroglobulin, thyroperoxidase, and Na+/I- symporter
Authors: Neumann, S Willgerodt, H Ackermann, F Reske, A Jung, M Reis, A Paschke, R
Citation: S. Neumann et al., Linkage of familial euthyroid goiter to the multinodular goiter-1 locus and exclusion of the candidate genes thyroglobulin, thyroperoxidase, and Na+/I- symporter, J CLIN END, 84(10), 1999, pp. 3750-3756
Autosomal dominant nonautoimmune hyperthyroidism - Clinical features - diagnosis - therapy
Authors: Fuhrer, D Mix, M Willgerodt, H Holzapfel, HP Von Petrykowski, W Wonerow, P Paschke, R
Citation: D. Fuhrer et al., Autosomal dominant nonautoimmune hyperthyroidism - Clinical features - diagnosis - therapy, EXP CL E D, 106, 1998, pp. S10-S15
Catch-up growth after childhood-onset substitution in primary hypothyroidism: Is it a guide towards optimal growth hormone treatment in idiopathic growth hormone deficiency?
Authors: Ranke, MB Schwarze, CP Mohnike, K von Muhlendahl, KE Keller, E Willgerodt, H Kiess, W
Citation: Mb. Ranke et al., Catch-up growth after childhood-onset substitution in primary hypothyroidism: Is it a guide towards optimal growth hormone treatment in idiopathic growth hormone deficiency?, HORMONE RES, 50(5), 1998, pp. 264-270
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