Multiple Endocrine Neoplasias in the Era of Translational Medicine

Autor: C. A. Stratakis, S. J. Marx

Publikováno v: Hormone and Metabolic Research. 37:343-346

Medicine is an ever changing art, continuously adjusting to the shifting principles of philosophy and constant discoveries of science; it was beautifully said by Hippocrates: "... medicine does not do the same thing at this moment and the next..." Un

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b06825d2bd0e375c4079487da54d02f3
https://doi.org/10.1055/s-2005-870183

Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the third international workshop

Autor: R. Eastell, A. Arnold, M. L. Brandi, E. M. Brown, P. D'Amour, D. A. Hanley, D. Sudhaker Rao, M. R. Rubin, D. Goltzman, S. J. Silverberg, S. J. Marx, M. Peacock, L. Mosekilde, R. Bouillon, E. M. Lewiecki

Publikováno v: Eastell, R, Arnold, A, Brandi, M L, Brown, E M, D'Amour, P, Hanley, D A, Rao, D S, Rubin, M R, Goltzman, D, Silverberg, S J, Marx, S J, Peacock, M, Mosekilde, L, Bouillon, R & Lewiecki, E M 2009, ' Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the third international workshop ', Journal of Clinical Endocrinology and Metabolism, vol. 94, no. 2, pp. 340-50 . https://doi.org/10.1210/jc.2008-1758

Udgivelsesdato: 2009-Feb OBJECTIVE: Asymptomatic primary hyperparathyroidism (PHPT) is a common clinical problem. The purpose of this report is to guide the use of diagnostic tests for this condition in clinical practice. PARTICIPANTS: Interested pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed4dc120cb1e9640fc43ece31141d5dd
https://pubmed.ncbi.nlm.nih.gov/19193909

Study of the multiple endocrine neoplasia type 1, growth hormone-releasing hormone receptor, Gs alpha, and Gi2 alpha genes in isolated familial acromegaly

Autor: B H, Jorge, S K, Agarwal, V S, Lando, R, Salvatori, R R, Barbero, N, Abelin, M A, Levine, S J, Marx, S P, Toledo

Publikováno v: The Journal of clinical endocrinology and metabolism. 86(2)

Familial acromegaly may occur as an isolated pituitary disorder or as a feature of hereditary syndromes, such as multiple endocrine neoplasia type 1 (MEN1) or the Carney complex. Herein, we characterized a newly identified kindred with isolated acrom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::aa8376ca1e68e82c635f9dee4a7fa4f5
https://pubmed.ncbi.nlm.nih.gov/11158006

MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinoma

Autor: L V, Debelenko, J I, Swalwell, M J, Kelley, E, Brambilla, P, Manickam, G, Baibakov, S K, Agarwal, A M, Spiegel, S J, Marx, S C, Chandrasekharappa, F S, Collins, W D, Travis, M R, Emmert-Buck

Publikováno v: Genes, chromosomescancer. 28(1)

Neuroendocrine tumors of the lung consist of a spectrum of neoplasms, including typical carcinoids, atypical carcinoids, large-cell neuroendocrine carcinomas (LCNEC), and small-cell lung carcinomas (SCLC). We previously reported frequent inactivation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e51b08061743f970f93f0f992661a73e
https://pubmed.ncbi.nlm.nih.gov/10738303

Multiple endocrine neoplasia type 1: atypical presentation, clinical course, and genetic analysis of multiple tumors

Autor: A O, Vortmeyer, I A, Lubensky, M, Skarulis, G, Li, Y W, Moon, W S, Park, R, Weil, C, Barlow, A M, Spiegel, S J, Marx, Z, Zhuang

Publikováno v: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 12(9)

Multiple endocrine neoplasia type 1 (MEN1) is characterized by the development of endocrine tumors of the parathyroid and pituitary glands, pancreas, and duodenum. Less frequently occurring tumors associated with MEN1 include non-endocrine tumors suc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6ff3dc3fcca4196e815149ba5090cd29
https://pubmed.ncbi.nlm.nih.gov/10496602