Zobrazeno 1 - 10
of 15
pro vyhledávání: '"C W, Biermann"'
Autor:
C W, Biermann, T, Küchler
Publikováno v:
Der Urologe. Ausg. A. 38(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89527443ef192f0067ed3e708b679d39
https://pubmed.ncbi.nlm.nih.gov/10231945
https://pubmed.ncbi.nlm.nih.gov/10231945
Autor:
C. W. Biermann
Publikováno v:
Uroonkologie ISBN: 9783662107324
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfb644714c038e08e27e2f594a484288
https://doi.org/10.1007/978-3-662-10731-7_21
https://doi.org/10.1007/978-3-662-10731-7_21
Publikováno v:
Swiss surgery = Schweizer Chirurgie = Chirurgie suisse = Chirurgia svizzera. (6)
During the last 20 years important improvements in diagnosis, staging and indications as well as in operative and conservative treatments of urological malignancies have been achieved. In consequence the prognoses of patients with these cancers have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00ca1e7147d36666c81e80d6e1ca2427
https://pubmed.ncbi.nlm.nih.gov/8581813
https://pubmed.ncbi.nlm.nih.gov/8581813
Publikováno v:
Swiss surgery = Schweizer Chirurgie = Chirurgie suisse = Chirurgia svizzera. (6)
Malignant Fibrous Histiocytoma (MFH) is an unfrequent mesenchymal tumor first described by O'Brian in 1964 [1, 16]. The most common site of this malignancy is the limbs area and the retroperitoneum. Primary involvement of the kidney is extremely rare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f0a6dcee5e3ab3e790eae2e764ab0e36
https://pubmed.ncbi.nlm.nih.gov/8581814
https://pubmed.ncbi.nlm.nih.gov/8581814
Publikováno v:
Helvetica chirurgica acta. 60(6)
Malignancies of the biliary tract are rare diseases. Tumor inductions after radiotherapy are reported in several papers. We report about 3 cases with consecutive biliary tract carcinoma 18-32 years after manifestation of an urogenital carcinoma. All
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::002da8a156a2844d5a93b088f1d93eaa
https://pubmed.ncbi.nlm.nih.gov/7875994
https://pubmed.ncbi.nlm.nih.gov/7875994
Publikováno v:
Helvetica chirurgica acta. 60(6)
Malignant mesothelioma of the tunica vaginalis testis is an extremely rare tumor, with only 40 cases previously described in the literature. Treatment consists of inguinal orchiectomy with close-follow up [1]. Asbestose exposure, trauma and hydrocele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ffaefaa1c5d8d768db5ccf135293f97
https://pubmed.ncbi.nlm.nih.gov/7875993
https://pubmed.ncbi.nlm.nih.gov/7875993
Autor:
C W, Biermann, G, Rutishauser
Publikováno v:
Scandinavian journal of urology and nephrology. 28(3)
A 41-year-old man with Marfan syndrome was found to have polycystic renal disease and underwent emergency surgery for dissecting aneurysm of the ascending aorta. To our knowledge only two cases of this rare combination of hereditary disorders have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2b0d41dc3e3cc61e62833b76682081c
https://pubmed.ncbi.nlm.nih.gov/7817174
https://pubmed.ncbi.nlm.nih.gov/7817174
Publikováno v:
Helvetica chirurgica acta. 59(3)
In 1872 the Viennese dermatologist Moritz Kaposi first described a pigment sarcoma of the skin. A modification of the epidemiology and the follow-up results in the accumulation of reports about the Kaposi-sarcoma after organ transplantation in the si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3afe03b3ea6feba71b1e9c96d7e94234
https://pubmed.ncbi.nlm.nih.gov/1464548
https://pubmed.ncbi.nlm.nih.gov/1464548
Publikováno v:
Helvetica chirurgica acta. 59(3)
For the first time Bernhard Marfan described the Marfan-Syndrome in 1896; it is a meso- and ectodermed variety with the conducting symptom of "arachnodactyly". Marfan-Syndrome is an autosomal dominant hereditary disorder with high penetrance and vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4dce5da58010eebe56b7b0aa7daac172
https://pubmed.ncbi.nlm.nih.gov/1464550
https://pubmed.ncbi.nlm.nih.gov/1464550
Publikováno v:
Helvetica chirurgica acta. 59(3)
Malignant mesothelioma of the tunica vaginalis testis is an extremely rare tumor, with only 37 cases previously described in the literature. Treatment consists of inguinal orchiectomy with close follow-up [1]. Asbestos exposure, trauma and hydrocele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05aa6b36692ae7e1a76e677f89979b74
https://pubmed.ncbi.nlm.nih.gov/1464547
https://pubmed.ncbi.nlm.nih.gov/1464547