Results 71 to 80 of about 117,411 (195)
Frontiers in Endocrinology, 2015 Adrenocortical tumors (ACT) in children are very rare and are most frequently diagnosed in the context of the Li-Fraumeni syndrome, a multiple cancer syndrome linked to germline mutations of the tumor suppressor gene TP53 with loss of heterozygosity in ...
Enzo eLalli, Bonald C. Figueiredo
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Adrenal lipomatous tumours: a 30 year clinicopathological experience at a single institution [PDF]
, 2001 AIMS: Fatty tumours of the adrenal gland are uncommon and their features have received little attention in the literature. The aim of this study is to analyse the features of adrenal lipomatous tumours.
Lam, AKY, Lo, CY
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S. E. polyoma virus: A provocative discovery [PDF]
, 1960 Thesis (M.D.)—Boston ...
Cohen, Stafford
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GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior [PDF]
, 2017 Background: Discrimination between benign and malignant tumors is a challenging process in pediatric adrenocortical tumors. New insights in the metabolic profile of pediatric adrenocortical tumors may contribute to this distinction, predict prognosis, as
Allolio +60 more
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Evaluation of adrenal tumors and analysis of the metabolic profile of patients with incidentaloma [PDF]
Revista do Colégio Brasileiro de CirurgiõesIntroduction: Advances in imaging methods have led to an increasingly frequent diagnosis of adrenal gland lesions as incidental findings. Despite progress in this field, there is still limited information regarding the epidemiology of the clinical and ...
PEDRO VICTOR GONÇALVES MONTALVÃO +5 more
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Adrenal myelolipoma associated with cholelithiasis
Indian Journal of Urology, 2001 Myelolipomas are usually as ymptomatic and discovered incidentally or at autopsy. They are rare benign adrenal neoplasms, characterized by the presence of adipose tissue and elements of haematopoietic tissue in various degrees of differentiation ...
Dilip K Kar +7 more
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Dichlorvos Critical Evaluation [PDF]
, 1999 Critical Evaluation of the breast cancer risk of dichlorvosNew York State Department of Health, and the U.S. Department of Agriculture-CSREES, Project no.
Gandhi, Renu, Snedeker, Suzanne M.
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Symptomatic ovarian steroid cell tumor not otherwise specified in a post-menopausal woman
Rare Tumors, 2016 Steroid cell tumor not otherwise specified (NOS) is a rare subtype of sex cord stromal tumor of the ovary and contributes less than 0.1% of all ovarian neoplasms.
Neha Sood +4 more
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Texture image analysis in differentiating malignant from benign adrenal cortical tumors in children and adults [PDF]
, 2009 OBJECTIVE: To investigate the possible role of chromatin texture parameters, nuclear morphology, DNA ploidy and clinical functional status in discriminating benign from malignant adrenocortical tumors (ACT).
Castelo, A. +7 more
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Primary renal teratoma: a rare entity [PDF]
, 2013 : Teratomas are neoplasms that arise from pluripotent cells and can differentiate along one or more embryonic germ lines. Renal teratoma is an exceedingly rare condition.
Afaf Amarti +7 more
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