Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maran Ilanchezhian"'
Autor:
Maran Ilanchezhian, Diana Grace Varghese, John W. Glod, Karlyne M. Reilly, Brigitte C. Widemann, Yves Pommier, Rosandra N. Kaplan, Jaydira Del Rivero
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Adrenocortical carcinoma (ACC) is a rare endocrine malignancy of the adrenal gland with an unfavorable prognosis. It is rare in the pediatric population, with an incidence of 0.2-0.3 patients per million in patients under 20 years old. It is primaril
Externí odkaz:
https://doaj.org/article/c2b0dfd5f57441c2b815a691d120ab2b
Autor:
Victoria L. Anderson, David J. Liewehr, Karlyne M. Reilly, Elliot Levy, Michal Mauda Havanuk, Bradford J. Wood, Brigitte C. Widemann, Ahmad Shafiei, Jaydira Del Rivero, Choung D. Hoang, Elizabeth C. Jones, David Venzon, Maran Ilanchezhian, Maureen Edgerly, Sarah N. Fuller, Hadi Bagheri
Publikováno v:
Current Oncology, Vol 28, Iss 370, Pp 4357-4366 (2021)
Current Oncology; Volume 28; Issue 6; Pages: 4357-4366
Current Oncology
Current Oncology; Volume 28; Issue 6; Pages: 4357-4366
Current Oncology
Adrenocortical carcinoma (ACC) is a rare malignancy with an overall unfavorable prognosis. Clinicians treating patients with ACC have noted accelerated growth in metastatic liver lesions that requires rapid intervention compared to other metastatic l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c4748d49a6f1b2593f512ab4d9fbe20
https://www.mdpi.com/1718-7729/28/6/370
https://www.mdpi.com/1718-7729/28/6/370
Publikováno v:
Hormone and Metabolic Research. 52:588-597
Medullary Thyroid Carcinoma (MTC) is a rare neuroendocrine cancer that accounts for 1–2% of thyroid cancers in the United States (U.S.). While most cases are sporadic, 25% of MTC cases are hereditary. These hereditary cases occur in the setting of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49324cb35b1151343e5791e893f247b4
https://doi.org/10.1055/a-1145-8479
https://doi.org/10.1055/a-1145-8479
Autor:
Jaydira Del Rivero, Brigitte C. Widemann, Amanda Carbonell, Prashant Chittiboina, Maran Ilanchezhian, Reinier Alvarez
Von Hippel-Lindau disease is an inherited, autosomal dominant tumor predisposition syndrome which leads to susceptibility for developing hemangioblastomas of the central nervous system and retina, as well as other tumor types. No approved systemic th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27782bd398d50c5ebbc4a9f0ba726f6f
https://doi.org/10.21203/rs.3.rs-330233/v1
https://doi.org/10.21203/rs.3.rs-330233/v1
Autor:
Brigitte C. Widemann, David Venzon, Jaydira Del Rivero, Joseph R. Fontana, Les R. Folio, John Glod, Alexander Ling, Deborah Allen, Sarah N. Fuller, Maran Ilanchezhian
Publikováno v:
J Clin Endocrinol Metab
Context Multiple endocrine neoplasia type 2B (MEN2B) is a rare cancer predisposition syndrome resulting from an autosomal-dominant germline mutation of the RET proto-oncogene. No prior studies have investigated pulmonary function in patients with MEN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c18797b14e486b495531c040b554e0
https://europepmc.org/articles/PMC7365699/
https://europepmc.org/articles/PMC7365699/
Autor:
Taryn Allen, Fernanda I. Arnaldez, Deborah Allen, Jaydira Del Rivero, Laura Wisch, Andy Gillespie, John Glod, Brigitte C. Widemann, Margarita Raygada, Maran Ilanchezhian, Barbara J. Thomas, Sarah N. Fuller, DePollar Sherri, Lori Weiner, Karlyne M. Reilly
Publikováno v:
Journal of the Endocrine Society
Introduction: Endocrine malignancies, as well as all pediatric cancers, are considered rare tumors, defined as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::add0b90286c2982a9f3448b1624538fb
https://doi.org/10.1210/js.2019-sun-341
https://doi.org/10.1210/js.2019-sun-341
Autor:
Constantine A. Stratakis, John Glod, Margarita Raygada, Sarah N. Fuller, Markku Miettinen, Maran Ilanchezhian, Fernanda I. Arnaldez, Paul S. Meltzer, Keith Killian
Publikováno v:
Journal of Clinical Oncology. 37:11033-11033
11033 Background: Gastrointestinal Stromal Tumors are the most common malignancy in the GI tract. While the vast majority exhibit somatic mutations in KIT and PDGFRA, approximately 15% of GIST patients do not have this feature. This group of KIT and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caa7417e462fc356695fc55f7fe7e343
https://doi.org/10.1200/jco.2019.37.15_suppl.11033
https://doi.org/10.1200/jco.2019.37.15_suppl.11033
Publikováno v:
Journal of Clinical Oncology. 37:e16125-e16125
e16125 Background: Adrenocortical carcinoma (ACC) is a rare tumor with an incidence of 1.5–2 per million people per year. It has a poor prognosis with an overall 5-year mortality of 75-80%. The treatment of choice for a localized primary or recurre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60196ba4c0c86cf383ff6ea1e7085629
https://doi.org/10.1200/jco.2019.37.15_suppl.e16125
https://doi.org/10.1200/jco.2019.37.15_suppl.e16125