Literature DB >> 24756

Multiple endocrine adenomatosis: in support of the common origin theories.

K L Janson, J A Roberts, M Varela.   

Abstract

Herein we give clinical support to the theory of a common origin of multiple endocrine adenomatosis. Accurate clinical evaluation of a patient suspected to have endocrine neoplasia requires the search for a much wider range of potential endocrine tumors. Such an approach is now made possible by the radioimmunoassay. Chromosome patterns and histocompatibility antigens are reviewed in a family with the disease.

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Year:  1978        PMID: 24756     DOI: 10.1016/s0022-5347(17)57420-0

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  3 in total

Review 1.  The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors.

Authors:  Paraskevi Xekouki; Ana Brennand; Ben Whitelaw; Karel Pacak; Constantine A Stratakis
Journal:  Horm Metab Res       Date:  2018-10-01       Impact factor: 2.936

2.  Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects?

Authors:  Paraskevi Xekouki; Constantine A Stratakis
Journal:  Endocr Relat Cancer       Date:  2012-10-30       Impact factor: 5.678

Review 3.  Coexistence of a pituitary macroadenoma and pheochromocytoma--a case report and review of the literature.

Authors:  Suzanne M Breckenridge; Amir H Hamrahian; Charles Faiman; John Suh; Richard Prayson; Marc Mayberg
Journal:  Pituitary       Date:  2003       Impact factor: 4.107

  3 in total

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