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Results: 1-22 |
Results: 22

Authors: Ranke, MB Schweizer, R Elmlinger, MW Weber, K Binder, G Schwarze, CP Wollmann, HA
Citation: Mb. Ranke et al., Relevance of IGF-I, IGFBP-3, and IGFBP-2 measurements during GH treatment of GH-deficient and non-GH-deficient children and adolescents, HORMONE RES, 55(3), 2001, pp. 115-124

Authors: Eggermann, T Mergenthaler, S Eggermann, K Albers, A Linnemann, K Fusch, C Ranke, MB Wollmann, HA
Citation: T. Eggermann et al., Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients, J MED GENET, 38(2), 2001, pp. 86-89

Authors: Elmlinger, MW Mayer, I Schnabel, D Schuett, BS Diesing, D Romalo, G Wollmann, HA Weidemann, W Spindler, KD Ranke, MB Schweikert, HU
Citation: Mw. Elmlinger et al., Decreased expression of IGF-II and its binding protein, IGF-binding protein-2, in genital skin fibroblasts of patients with complete androgen insensitivity syndrome compared with normally virilized males, J CLIN END, 86(10), 2001, pp. 4741-4746

Authors: Eggermann, T Kloos, P Mergenthaler, S Eggermann, K Dobos, M Ranke, MB Wollmann, HA
Citation: T. Eggermann et al., IRS1 and GRB2 as members of the IGF signal transduction pathway are not associated with intrauterine growth retardation and Silver-Russell syndrome, CLIN GENET, 59(5), 2001, pp. 371-373

Authors: Mergenthaler, S Hitchins, MP Blagitko-Dorfs, N Monk, D Wollmann, HA Ranke, MB Ropers, HH Apostolidou, S Stanier, P Preece, MA Eggermann, T Kalscheuer, VM Moore, GE
Citation: S. Mergenthaler et al., Conflicting reports of imprinting status of human GRB10 in developing brain: How reliable are somatic cell hybrids for predicting allelic origin of expression?, AM J HU GEN, 68(2), 2001, pp. 543-544

Authors: Blagitko, N Mergenthaler, S Schulz, U Wollmann, HA Craigen, W Eggermann, T Ropers, HH Kalscheuer, VM
Citation: N. Blagitko et al., Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion, HUM MOL GEN, 9(11), 2000, pp. 1587-1595

Authors: Iliev, DI Petruch, UR Ranke, MB Binder, G Leriche, C Strotbek, G Wollmann, HA
Citation: Di. Iliev et al., Transient pseudohypoaldosteronism with complex malformation of internal genitalia - A case report, HORMONE RES, 54(3), 2000, pp. 149-152

Authors: Ranke, MB Schweizer, R Elmlinger, MW Weber, K Binder, G Schwarze, CP Wollmann, HA
Citation: Mb. Ranke et al., Significance of basal IGF-I, IGFBP-3 and IGFBP-2 measurements in the diagnostics of short stature in children, HORMONE RES, 54(2), 2000, pp. 60-68

Authors: Schweizer, R Ranke, MB Binder, G Herdach, F Zapadlo, M Grauer, ML Schwarze, CP Wollmann, HA
Citation: R. Schweizer et al., Experience with growth hormone therapy in Turner syndrome in a single centre: Low total height gain, no further gains after puberty onset and unchanged body proportions, HORMONE RES, 53(5), 2000, pp. 228-238

Authors: Wollmann, HA
Citation: Ha. Wollmann, Growth hormone and growth factors during perinatal life, HORMONE RES, 53, 2000, pp. 50-54

Authors: Seibold-Weiger, K Wollmann, HA Ranke, MB Speer, CP
Citation: K. Seibold-weiger et al., Plasma concentrations of the carboxyterminal propeptide of type I procollagen (PICP) in preterm neonates from birth to term, PEDIAT RES, 48(1), 2000, pp. 104-108

Authors: Ranke, MB Dorr, HG Stahnke, N Partsch, CJ Schwarz, HP Wollmann, HA Bettendorf, M Hauffa, BP
Citation: Mb. Ranke et al., Therapy of growth deficiency with growth hormone. Developments 10 years after the introduction of recombinant growth hormone, MONATS KIND, 148(8), 2000, pp. 746-761

Authors: de Zegher, F Albertsson-Wikland, K Wollmann, HA Chatelain, P Chaussain, JL Lofstrom, A Jonsson, B Rosenfeld, RG
Citation: F. De Zegher et al., Growth hormone treatment of short children born small for gestational age:Growth responses with continuous and discontinuous regimens over 6 years, J CLIN END, 85(8), 2000, pp. 2816-2821

Authors: Mergenthaler, S Wollmann, HA Burger, B Eggermann, K Kaiser, P Ranke, MB Schwanitz, G Eggermann, T
Citation: S. Mergenthaler et al., Formation of uniparental disomy 7 delineated from new cases and a UPD7 case after trisomy 7 rescue. Presentation of own results and review of the literature, ANN GENET, 43(1), 2000, pp. 15-21

Authors: Schwarze, CP Wollmann, HA Binder, G Ranke, MB
Citation: Cp. Schwarze et al., Short-term increments of insulin-like growth factor I (IGF-I) and IGF-binding protein-3 predict the growth response to growth hormone (GH) therapy inGH-sensitive children, ACT PAEDIAT, 88, 1999, pp. 200-208

Authors: Nagel, BHP Mortier, W Elmlinger, M Wollmann, HA Schmitt, K Ranke, MB
Citation: Bhp. Nagel et al., Short stature in Duchenne muscular dystrophy: a study of 34 patients, ACT PAEDIAT, 88(1), 1999, pp. 62-65

Authors: Holterhus, PM Sinnecker, GHG Wollmann, HA Struve, D Homburg, N Kruse, K Hiort, O
Citation: Pm. Holterhus et al., Expression of two functionally different androgen receptors in a patient with androgen insensitivity, EUR J PED, 158(9), 1999, pp. 702-706

Authors: Ranke, MB Wollmann, HA Savage, MO
Citation: Mb. Ranke et al., Experience with insulin-like growth factor I (IGF-I) treatment of growth hormone insensitivity syndrome (GHIS), J PED END M, 12, 1999, pp. 259-266

Authors: Ranke, MB Schweizer, R Wollmann, HA Schwarze, P
Citation: Mb. Ranke et al., Dosing of growth hormone in growth hormone deficiency, HORMONE RES, 51, 1999, pp. 70-74

Authors: Elmlinger, MW Grund, R Buck, M Wollmann, HA Feist, N Weber, MM Speer, CP Ranke, MB
Citation: Mw. Elmlinger et al., Limited proteolysis of the IGF binding protein-2 (IGFBP-2) by a specific serine protease activity in early breast milk, PEDIAT RES, 46(1), 1999, pp. 76-81

Authors: Eggermann, K Wollmann, HA Binder, G Kaiser, P Ranke, MB Eggermann, T
Citation: K. Eggermann et al., Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely, ANN GENET, 42(2), 1999, pp. 117-121

Authors: Eggermann, K Wollmann, HA Tomiuk, J Ranke, MB Kaiser, P Eggermann, T
Citation: K. Eggermann et al., Screening for mutations in the promoter and the coding region of the IGFBP1 and IGFBP3 genes in Silver-Russell syndrome patients, HUMAN HERED, 49(3), 1999, pp. 123-128
Risultati: 1-22 |