Muir-Torre-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Muir-Torre-Syndrom" in German language version.

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bmj.com

jmg.bmj.com

  • E. Mangold, C. Pagenstecher, M. Leister, M. Mathiak, A. Rütten: A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. In: Journal of Medical Genetics. Band 41, Nr. 7, 1. Juli 2004, ISSN 0022-2593, S. 567–572, doi:10.1136/jmg.2003.012997, PMID 15235030, PMC 1735835 (freier Volltext) – (bmj.com [abgerufen am 12. August 2022]).

doi.org

  • C. D. South, H. Hampel, I. Comeras, J. A. Westman, W. L. Frankel, A. de la Chapelle: The frequency of Muir-Torre syndrome among Lynch syndrome families. In: Journal of the National Cancer Institute. Band 100, Nummer 4, Februar 2008, S. 277–281, doi:10.1093/jnci/djm291, PMID 18270343.
  • E. Mangold, C. Pagenstecher, M. Leister, M. Mathiak, A. Rütten: A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. In: Journal of Medical Genetics. Band 41, Nr. 7, 1. Juli 2004, ISSN 0022-2593, S. 567–572, doi:10.1136/jmg.2003.012997, PMID 15235030, PMC 1735835 (freier Volltext) – (bmj.com [abgerufen am 12. August 2022]).
  • L. Orta, D. S. Klimstra, J. Qin, P. Mecca, L. H. Tang, K. J. Busam, J. Shia: Towards identification of hereditary DNA mismatch repair deficiency: sebaceous neoplasm warrants routine immunohistochemical screening regardless of patient's age or other clinical characteristics. In: The American journal of surgical pathology. Band 33, Nummer 6, Juni 2009, S. 934–944, doi:10.1097/PAS.0b013e318199edca, PMID 19342947.
  • J. Rüschoff, H. U. Schildhaus, J. H. Rüschoff, K. Jöhrens, T. Bocker-Edmonston, W. Dietmaier, H. Bläker, G. Baretton, D. Horst, M. Dietel, A. Hartmann, F. Klauschen, S. Merkelbach-Bruse, A. Stenzinger, S. Schöniger, M. Tiemann, W. Weichert, R. Büttner: [Testing deficient mismatch repair and microsatellite instability : A focused update. German version]. In: Pathologie. Band 44, Nummer 5, September 2023, S. 301–310, doi:10.1007/s00292-023-01209-1, PMID 37548948, PMC 1045723 (freier Volltext) (Review).
  • T. Graefe, U. Wollina, H. Schulz, W. Burgdorf: Muir-Torre syndrome - treatment with isotretinoin and interferon alpha-2a can prevent tumour development. In: Dermatology. Band 200, Nummer 4, 2000, S. 331–333, doi:10.1159/000018399, PMID 10894967.
  • R. L. Spielvogel, R. L. DeVillez, L. C. Roberts: Oral isotretinoin therapy for familial Muir-Torre syndrome. In: Journal of the American Academy of Dermatology. Band 12, Nummer 3, März 1985, S. 475–480, doi:10.1016/s0190-9622(85)70066-7, PMID 3857234.

medscape.com

emedicine.medscape.com

  • Victor G. Prieto: Muir-Torre Syndrome. In: emedicine, 2020

nih.gov

ncbi.nlm.nih.gov

  • C. D. South, H. Hampel, I. Comeras, J. A. Westman, W. L. Frankel, A. de la Chapelle: The frequency of Muir-Torre syndrome among Lynch syndrome families. In: Journal of the National Cancer Institute. Band 100, Nummer 4, Februar 2008, S. 277–281, doi:10.1093/jnci/djm291, PMID 18270343.
  • E. Mangold, C. Pagenstecher, M. Leister, M. Mathiak, A. Rütten: A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. In: Journal of Medical Genetics. Band 41, Nr. 7, 1. Juli 2004, ISSN 0022-2593, S. 567–572, doi:10.1136/jmg.2003.012997, PMID 15235030, PMC 1735835 (freier Volltext) – (bmj.com [abgerufen am 12. August 2022]).
  • P. R. Cohen, S. R. Kohn, R. Kurzrock: Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome. In: The American journal of medicine. Band 90, Nummer 5, Mai 1991, S. 606–613, PMID 2029018 (Review).
  • L. Orta, D. S. Klimstra, J. Qin, P. Mecca, L. H. Tang, K. J. Busam, J. Shia: Towards identification of hereditary DNA mismatch repair deficiency: sebaceous neoplasm warrants routine immunohistochemical screening regardless of patient's age or other clinical characteristics. In: The American journal of surgical pathology. Band 33, Nummer 6, Juni 2009, S. 934–944, doi:10.1097/PAS.0b013e318199edca, PMID 19342947.
  • J. Rüschoff, H. U. Schildhaus, J. H. Rüschoff, K. Jöhrens, T. Bocker-Edmonston, W. Dietmaier, H. Bläker, G. Baretton, D. Horst, M. Dietel, A. Hartmann, F. Klauschen, S. Merkelbach-Bruse, A. Stenzinger, S. Schöniger, M. Tiemann, W. Weichert, R. Büttner: [Testing deficient mismatch repair and microsatellite instability : A focused update. German version]. In: Pathologie. Band 44, Nummer 5, September 2023, S. 301–310, doi:10.1007/s00292-023-01209-1, PMID 37548948, PMC 1045723 (freier Volltext) (Review).
  • T. Graefe, U. Wollina, H. Schulz, W. Burgdorf: Muir-Torre syndrome - treatment with isotretinoin and interferon alpha-2a can prevent tumour development. In: Dermatology. Band 200, Nummer 4, 2000, S. 331–333, doi:10.1159/000018399, PMID 10894967.
  • R. L. Spielvogel, R. L. DeVillez, L. C. Roberts: Oral isotretinoin therapy for familial Muir-Torre syndrome. In: Journal of the American Academy of Dermatology. Band 12, Nummer 3, März 1985, S. 475–480, doi:10.1016/s0190-9622(85)70066-7, PMID 3857234.

omim.org

orpha.net

zdb-katalog.de

  • E. Mangold, C. Pagenstecher, M. Leister, M. Mathiak, A. Rütten: A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. In: Journal of Medical Genetics. Band 41, Nr. 7, 1. Juli 2004, ISSN 0022-2593, S. 567–572, doi:10.1136/jmg.2003.012997, PMID 15235030, PMC 1735835 (freier Volltext) – (bmj.com [abgerufen am 12. August 2022]).