Zobrazeno 1 - 10
of 51
pro vyhledávání: '"MULTIPLE ENDOCRINE NEOPLASIA TYPE II"'
Publikováno v:
Эндокринная хирургия, Vol 9, Iss 3, Pp 44-48 (2015)
Syndrome Sipple is the second name of the syndrome of multiple endocrine neoplasia type II (MEN2A). In 1961 J.H. Sipple described several relatives with medullary thyroid cancer, feohromotsytoma and hyperparathyroidism. The following observation is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be5f431c568d5d39ca6e43e733107839
https://surg-endojournals.ru/serg/article/viewFile/7678/5611
https://surg-endojournals.ru/serg/article/viewFile/7678/5611
Autor:
Tirtha K. Das, Ross L. Cagan
Publikováno v:
Thyroid. 20:689-695
Multiple endocrine neoplasia type II (MEN2) is a rare but aggressive cancer for which no effective treatment currently exists. A Drosophila model was developed to identify novel genetic modifier loci of oncogenic RET, as well as to provide a whole an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::748d87b0221093ec70d47af55521b028
https://doi.org/10.1089/thy.2010.1637
https://doi.org/10.1089/thy.2010.1637
Publikováno v:
Journal of the American Academy of Dermatology. 55:341-344
Pheochromocytoma is a rare tumor originating from neuroectodermic cells. Only 10% of these tumors are malignant. There are many familial forms of this tumor, including multiple endocrine neoplasia type II, Von Hippel-Lindau syndrome, and neurofibroma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67990e294fb45948a932422cfd632cac
https://doi.org/10.1016/j.jaad.2005.11.1080
https://doi.org/10.1016/j.jaad.2005.11.1080
Publikováno v:
Current Urology Reports. 2:19-23
Most adrenal tumors are found incidentally and appear as small solitary nodules on abdominal imaging. Occasionally, work-up demonstrates multifocal or bilateral adrenal tumors. Certain patients are predisposed to multiple lesions, such as those with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4f9a37fa83e5a3c48f1b4c56cc6ab2
https://doi.org/10.1007/s11934-001-0021-0
https://doi.org/10.1007/s11934-001-0021-0
Autor:
Stephen R. Grobmyer, Craig D. Shriver, James M. Woodruff, Murray F. Brennan, Jose G. Guillem, Diarmuid S. O'Riordain
Publikováno v:
Diseases of the Colon & Rectum. 42:1216-1219
Multiple endocrine neoplasia type 2B is best known for its endocrine manifestations and typical phenotype. The gastrointestinal manifestations, however, are also an important and commonly unrecognized component of the syndrome. We present four cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b485c8351101b48d88347149210d4719
https://doi.org/10.1007/bf02238578
https://doi.org/10.1007/bf02238578
Autor:
R. Tratzmüller, H. Vogt, P. H. Heidemann, U. Irle, D. Knorr, Wolfgang Höppner, Henning Dralle
Publikováno v:
Monatsschrift Kinderheilkunde. 147:733-743
Hintergrund: Die multiple endokrine Neoplasie (MEN) Typ 2 mit ihren Subtypen MEN Typ 2a, Typ 2b und dem familiaren medullaren Schilddrusenkarzinom ist eine seltene autosomal-dominant erbliche Tumorerkrankung, die auf aktivierenden Keimbahnmutationen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24bcee440dc7ae5b171a7fc28388f1c0
https://doi.org/10.1007/s001120050489
https://doi.org/10.1007/s001120050489
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 59:643-647
DNA testing is of great importance in families with multiple endocrine neoplasia (MEN) type 2A to identify non-mutant carrying family members and asymptomatic mutation carriers, and also to confirm the diagnosis in patients who already show clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9365c6ad6f928e907c5b5cc28a5ac2
https://doi.org/10.1080/00365519950185148
https://doi.org/10.1080/00365519950185148
Autor:
Virpi V. Smith, Charis Eng, Peter J. Milla, Bruce G. Robinson, Michael A. Patton, Bruce A.J. Ponder, Deborah J. Marsh, Deon J. Venter, Melissa C. Southey, Chung Wo Chow
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:4191-4194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::334150a0c12b80ce5bbae05ffea04a78
https://doi.org/10.1210/jcem.83.12.5352
https://doi.org/10.1210/jcem.83.12.5352
Autor:
Xavier Matias-Guiu
Publikováno v:
Advances in Anatomic Pathology. 5:196-201
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b53415a0fd5adb3ddbfb58487f22014a
https://doi.org/10.1097/00125480-199805000-00058
https://doi.org/10.1097/00125480-199805000-00058
Autor:
Joseph A. Majzoub, Catherine M. Gordon, Bruce G. Robinson, Deborah J. Marsh, Charis Eng, John B. Mulliken, Bruce A.J. Ponder
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:17-20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6f6d2efaada1a6f3f0787c2a3ff0187
https://doi.org/10.1210/jcem.83.1.4504
https://doi.org/10.1210/jcem.83.1.4504