Results 41 to 50 of about 622,771 (208)

18F-FDG PET-CT Evaluation of Primary Adrenal Ewing Sarcoma with Venous Thrombosis: An Unusual Presentation

World Journal of Nuclear Medicine, 2022
Ewing sarcoma (EWS) is primarily an osseous malignancy of childhood and young adults. Extraskeletal occurrence is less frequent and primary adrenal involvement is an even rare presentation.
Debdip Roy, Melvika Pereira, Divya Shivdasani, Natasha Singh   +3 more
doaj   +1 more source

Machine Learning Applications in Endocrinology and Metabolism Research: An Overview [PDF]

Endocrinology and Metabolism, 2020
Machine learning (ML) applications have received extensive attention in endocrinology research during the last decade. This review summarizes the basic concepts of ML and certain research topics in endocrinology and metabolism where ML principles have ...
Namki Hong, Heajeong Park, Yumie Rhee
doaj   +1 more source

Mifepristone reduces insulin resistance in patient volunteers with adrenal incidentalomas that secrete low levels of cortisol : a pilot study [PDF]

, 2013
Background: Incidental adrenal masses are commonly detected during imaging for other pathologies. 10% of the elderly population has an ‘adrenal incidentaloma’, up to 20% of these show low-grade autonomous cortisol secretion and 60% of patients with ...
Rita Chadarevian, Eastell, R. (Richard), Richard J Ross, Richard Eastell (153287), Chadarevian, Rita, Debono, M., Newell-Price, John, Rita Chadarevian (399995), Richard J. Ross (399996), Richard Eastell, Randeva, Harpal S., Chadarevian, R., John Newell-Price (399997), Newell-Price, J., Ross, R.J., Miguel Debono (399994), Ross, Richard J. M., Miguel Debono, John Newell-Price, Eastell, R., Eastell Richard, Debono Miguel, Newell-Price John, Ross Richard J., Chadarevian Rita   +24 more
core   +1 more source

A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of swiss ancestry with congenital lipoid adrenal hyperplasia [PDF]

, 2005
Context: Lipoid congenital adrenal hyperplasia (CAH) is the most severe form of CAH leading to impaired production of all adrenal and gonadal steroids.
Maret, A, Mullis, PE, Leheup, B, Flück, Christa E., Portrat-Doyen, Stéphanie, Achermann, JC, Mallet, D, Fluck, CE, Mullis, Primus-Eugen, Morel, Yves, Theintz, Gérald E., Theintz, GE, Leheup, Bruno, Achermann, John C., Morel, Y, Portrat-Doyen, S, Maret, Alexander, Mallet, Delphine, Portrat-Doyen, S., Maret, A., Leheup, B., Fluck, C. E., Mullis, P. E., Morel, Y., Achermann, J. C., Mallet, D., Theintz, G. E.   +26 more
core   +2 more sources

Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency [PDF]

, 2009
Context: Familial glucocorticoid deficiency (FGD) is an autosomal recessive disorder resulting from resistance to the action of ACTH on the adrenal cortex.
Racine, M, Naville, D., Nurnberg, G., Green, J, Metherell, L. A., Nurnberg, P, Krone, NP, Krone, N. P., Arlt, W, Tomlinson, Jeremy, Achermann, JC, Halaby, G, Tomlinson, J. W., Clark, A. J. L., Krone, Nils, Naville, D, Berney, D. M., Begeot, M., Huebner, A., Halaby, G., Green, J., Berney, DM, Clark, AJ, Lin, L, Lin, L., Racine, M., Arlt, Wiebke, Achermann, J. C., Arlt, W., Nurnberg, G, Metherell, LA, Tomlinson, JW, Begeot, M, Huebner, A, Nurnberg, P., Clark, AJL, Krone, Nils P, Green, Jane, Nuernberg, Peter, Tomlinson, Jeremy W, Begeot, Martine, Nuernberg, Gudrun, Racine, Michael, Clark, Adrian JL, Achermann, John C, Huebner, Angela, Lin, Lin, Halaby, George, Metherell, Louise A, Naville, Danielle, Berney, Dan M   +50 more
core   +1 more source

Preclinical Cushing's syndrome in adrenal incidentalomas [PDF]

, 1992
Adrenal tumors are usually diagnosed by clinical symptoms of hormone excess. The increasing use of ultrasound and computed tomography results in the detection of a substantial number of incidentally discovered adrenal tumors.
Winkelmann, W., Saeger, W., Krestin, G. P., Nieke, J., Allolio, B., Reincke, Martin   +5 more
core   +1 more source

European Society of Endocrinology Clinical Practice Guidelines on the Management of Adrenocortical Carcinoma in Adults, in collaboration with the European Network for the Study of Adrenal Tumors.

European Journal of Endocrinology, 2018
Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone producing tumor with variable prognosis. The purpose of these guidelines is to provide clinicians with best possible evidence-based recommendations for clinical management of ...
M. Fassnacht, O. Dekkers, T. Else, E. Baudin, A. Berruti, R. D. de Krijger, H. Haak, R. Mihai, G. Assié, M. Terzolo   +9 more
semanticscholar   +1 more source

Gene array analysis of adrenal glands in broiler chickens following ACTH treatment [PDF]

, 2009
Difference in adaptability responses to stress has been observed amongst bird species, strains, and individuals. Components of the HPA axis, one of the internal systems involved in homeostasis re-establishment following stress, could play a role in this ...
Young Kyoung Park, Couty, Michel, Bureau, Clara, Christelle Hennequet-Antier, Keun Hwa Lee, Michel Couty, Kwan Soo Ko, Clara Bureau, Jae-Hoon Song, Hennequet-Antier, Christelle, Daniel Guémené, Guémené, Daniel, Doo-Ryeon Chung, Hae Suk Cheong, Guemene, Daniel,, Hennequet Antier, Christelle, Guemene, Daniel, D., Bureau Clara, Couty Michel, Guémené Daniel, Hennequet-Antier Christelle, Bureau, Wafa-Clara   +21 more
core   +1 more source

Cutaneous lesions and other non-endocrine manifestations of Multiple Endocrine Neoplasia type 1 syndrome

Frontiers in Endocrinology, 2023
BackgroundMultiple Endocrine Neoplasia type 1 is a rare genetic syndrome mainly caused by mutations of MEN1 gene and characterized by a combination of several endocrine and non-endocrine manifestations.
Laura Pierotti, Elena Pardi, Elisa Dinoi, Paolo Piaggi, Simona Borsari, Simone Della Valentina, Chiara Sardella, Angela Michelucci, Maria Adelaide Caligo, Fausto Bogazzi, Claudio Marcocci, Claudio Marcocci, Filomena Cetani   +12 more
doaj   +1 more source

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline.

Journal of Clinical Endocrinology and Metabolism, 2018
Objective To update the congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency clinical practice guideline published by the Endocrine Society in 2010.
P. W. Speiser, W. Arlt, R. Auchus, Laurence S. Baskin, Gerard S. Conway, D. Merke, H. Meyer-Bahlburg, Walter L. Miller, M. Murad, Sharon E. Oberfield, P. White   +10 more
semanticscholar   +1 more source