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Results: 1-8 |
Results: 8
FDG-PET imaging for the staging and follow-up of small cell lung cancer
Authors: Schumacher, T Brink, I Mix, M Reinhardt, R Herget, G Digel, W Henke, M Moser, E Nitzsche, E
Citation: T. Schumacher et al., FDG-PET imaging for the staging and follow-up of small cell lung cancer, EUR J NUCL, 28(4), 2001, pp. 483-488
Metastatic lymph nodes in patients with cervical cancer: Detection with MRimaging and FDG PET
Authors: Reinhardt, MJ Ehritt-Braun, C Vogelgesang, D Ihling, C Hogerle, S Mix, M Moser, E Krause, TM
Citation: Mj. Reinhardt et al., Metastatic lymph nodes in patients with cervical cancer: Detection with MRimaging and FDG PET, RADIOLOGY, 218(3), 2001, pp. 776-782
Isolated GH deficiency with dominant inheritance: New mutations, new insights
Authors: Binder, G Keller, E Mix, M Massa, GG Stokvis-Brantsma, WH Wit, JM Ranke, MB
Citation: G. Binder et al., Isolated GH deficiency with dominant inheritance: New mutations, new insights, J CLIN END, 86(8), 2001, pp. 3877-3881
Impact of F-18-FDG-positron emission tomography for decision making in colorectal cancer recurrences
Authors: Imdahl, A Reinhardt, MJ Nitzsche, EU Mix, M Dingeldey, A Einert, A Baier, P Farthmann, EH
Citation: A. Imdahl et al., Impact of F-18-FDG-positron emission tomography for decision making in colorectal cancer recurrences, LANG ARCH S, 385(2), 2000, pp. 129-134
Reproducibility of PET brain mapping of cancer patients
Authors: Tashiro, M Juengling, FD Reinhardt, MJ Brink, I Hoegerle, S Mix, M Kubota, K Yamaguchi, K Itoh, M Sasaki, H Moser, E Nitzsche, EU
Citation: M. Tashiro et al., Reproducibility of PET brain mapping of cancer patients, PSYCHO-ONC, 9(2), 2000, pp. 157-163
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
Prader-Labhart-Willi syndrome with central precocious puberty and empty sella syndrome
Authors: Linnemann, K Schroder, C Mix, M Kruger, G Fusch, C
Citation: K. Linnemann et al., Prader-Labhart-Willi syndrome with central precocious puberty and empty sella syndrome, ACT PAEDIAT, 88(11), 1999, pp. 1295-1297
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
Risultati: 1-8 |