Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Richard A. Failor"'
Autor:
Xinxian Deng, He Fang, Asha Pathak, Angela M. Zou, Whitney Neufeld-Kaiser, Emily A. Malouf, Richard A. Failor, Fuki M. Hisama, Yajuan J. Liu
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundHypergonadotropic hypogonadism (HH) is characterized by low sex steroid levels and secondarily elevated gonadotropin levels with either congenital or acquired etiology. Genetic factors leading to HH have yet to be fully elucidated.MethodsHe
Externí odkaz:
https://doaj.org/article/3dc4d9f2c90a4f2f956fd8f281eb4c74
Autor:
Asha K. Pathak, MD, Gregory M. Cheeney, MD, Mara H. Rendi, MD, PhD, Renata R. Urban, MD, Richard A. Failor, MD, Alan Chait, MD
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 3, Pp 252-255 (2018)
ABSTRACT: Objective: We describe a case of co-existing Graves disease and struma carcinoid in a woman with an ovarian mass and history of hyperthyroidism.Methods: Patient history, presentation, diagnostic studies, and treatment are described.Results:
Externí odkaz:
https://doaj.org/article/6cdfddb1c25d46b0b6141b44c706674e
Autor:
Karl Cristie F Figuracion, Lia M Halasz, Ny-Ying Lam, Myron Goldberg, Joe Stuckey, Richard A Failor, Lindsey M Knowles, Samantha Artherholt, Brian Chou, Courtney E Francis, Kristin Knight, Maninder Kaur, Tatiana Sadak, Tresa McGranahan
Publikováno v:
Neurooncol Pract
AbstractAs a result of treatment and diagnosis, adults with primary or metastatic brain tumors experience comorbidities that impacts their health and well-being. The Children’s Oncology Group has guideline recommendations for childhood survivors of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e476bb6d1f751e9d91edcd712136a15
https://doi.org/10.1093/nop/npac053
https://doi.org/10.1093/nop/npac053
Publikováno v:
Journal of the Endocrine Society. 6:A186-A187
A 52-year-old African woman was found to have a pelvic mass at the age of 41. Following resection of small bowel tumors at the time, she was diagnosed with GIST and peritoneal metastases were confirmed. Despite treatment with imatinib, her disease pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b158ebce9a0d52c4c9ee456fce448790
https://doi.org/10.1210/jendso/bvac150.385
https://doi.org/10.1210/jendso/bvac150.385
Publikováno v:
Journal of the Endocrine Society
INTRO ACTH-secreting pheochromocytoma is rare, posing challenges in diagnosis and management. Here we report two cases with different presentations and pre-operative approaches. CASES Patient 1 A 59 yo female who presented for basal cell carcinoma re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d450b31c0e679fce9a1946502adf144
http://europepmc.org/articles/PMC7208103
http://europepmc.org/articles/PMC7208103
Autor:
Xinxian, Deng, He, Fang, Asha, Pathak, Angela M, Zou, Whitney, Neufeld-Kaiser, Emily A, Malouf, Richard A, Failor, Fuki M, Hisama, Yajuan J, Liu
Publikováno v:
Frontiers in Genetics
Background Hypergonadotropic hypogonadism (HH) is characterized by low sex steroid levels and secondarily elevated gonadotropin levels with either congenital or acquired etiology. Genetic factors leading to HH have yet to be fully elucidated. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52b3f72ab03382550b8da9fe554d49e1
https://pubmed.ncbi.nlm.nih.gov/33193636
https://pubmed.ncbi.nlm.nih.gov/33193636
Autor:
Richard A Failor, Asha K. Pathak, Alan Chait, Renata R. Urban, Mara H. Rendi, Gregory Cheeney
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 3, Pp 252-255 (2018)
Objective: We describe a case of co-existing Graves disease and struma carcinoid in a woman with an ovarian mass and history of hyperthyroidism.Methods: Patient history, presentation, diagnostic studies, and treatment are described.Results: A 59-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4dc93e1961476958fd8489f7c1ec7e8
https://doi.org/10.4158/accr-2017-0111
https://doi.org/10.4158/accr-2017-0111
Autor:
Luis F. Gonzalez-Cuyar, Richard A Failor, Patrick J. Cimino, Kristen S. Moe, Manuel Ferreira, Eun Kyung Koh, Jacob Ruzevick, Lorena A. Wright
Publikováno v:
Journal of Neuro-Oncology. 132:473-478
Head and neck paragangliomas are rare neuroendocrine tumors that arise from paraganglion cells of the parasympathetic nervous system. Paragangliomas arising from the midline skull base have only rarely been reported. Surgery is the mainstay of treatm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0324206f48c2c8a4d8417af0193a6140
https://doi.org/10.1007/s11060-017-2396-x
https://doi.org/10.1007/s11060-017-2396-x
Autor:
Kathryn T. Dinh, Richard A Failor
Publikováno v:
Journal of the Endocrine Society
Background: The incidence of bilateral macronodular adrenal hyperplasia (BMAH) is unknown, but growing in an era of increased utilization of imaging. Coexistence of BMAH and pheochromocytoma has not previously been reported. Clinical Case: A 63-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54fd2656dad17a186408fba44f459428
https://doi.org/10.1210/jendso/bvab048.330
https://doi.org/10.1210/jendso/bvab048.330
Autor:
Vladimir Valera Romero, Andreas G. Moraitis, Fady Hannah-Shmouni, Richard A Failor, Annabel Berthon, Maria J. Merino, Andrew P. Demidowich, Constantine A. Stratakis, Fabio R. Faucz, Spyridon A. Mastroyannis
Publikováno v:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 50(2)
Primary bilateral macronodular adrenocortical hyperplasia (PBMAH) is an uncommon cause of adrenal Cushing syndrome (CS) in which cortisol and occasionally other steroid hormones can be secreted under the influence of aberrantly expressed G-protein co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66705dc6dbeb3fb40ea7f3aae4a3ae0a
https://pubmed.ncbi.nlm.nih.gov/29183089
https://pubmed.ncbi.nlm.nih.gov/29183089