Results 51 to 60 of about 115,598 (311)
An exceedingly rare adrenal collision tumor: adrenal adenoma–metastatic breast cancer–myelolipoma
Journal of Community Hospital Internal Medicine Perspectives, 2017 Adrenal collision tumors (ACTs), in which distinct tumors coexist without histological intermingling in the same adrenal gland, are rare and their actual prevalence is unknown. ACTs commonly consist of adrenal cortical adenoma, myelolipoma, or metastatic
Dongyan Liu, Sahayini A. Kumar
doaj +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. +5 more
core
New directions for the treatment of adrenal insufficiency [PDF]
, 2015 The following funding bodies supported this work: Biotechnology and Biological Sciences Research Council (BBSRC BB/L00267/1, to LG), Rosetrees Trust (to LG), Barts and The London Charity (417/2235, to LG), EU COFUND (PCOFUND-GA-2013-608765, to LG and GRB)
Leonardo Guasti +10 more
core +1 more source
Advanced Science, EarlyView.This study establishes [68Ga]Ga‐DOTA‐AP9 as a first‐in‐human CD147‐targeted PET tracer with favorable safety and specific tumor uptake. Tracer accumulation correlates with CD147 expression in patients, enabling noninvasive quantification of CD147‐positive malignancies.
Xiaokun Ma +10 more
wiley +1 more source
Amuc_1473 Links Gut Microbes to Skeletal Homeostasis and Counteracts Multifactorial Osteoporosis
Advanced Science, EarlyView.Amuc_1473, a previously uncharacterized protein enriched in Akkermansia muciniphila‐derived extracellular vesicles, is identified as a gut–bone messenger that promotes osteogenesis and inhibits osteoclastogenesis by engaging transcriptional and translational regulators in bone cells.
Shan‐Shan Rao +28 more
wiley +1 more source
Untreated Congenital Adrenal Hyperplasia with 17-α Hydroxylase/17,20-Lyase Deficiency Presenting as Massive Adrenocortical Tumor [PDF]
Endocrinology and Metabolism, 2015 Congenital adrenal hyperplasia (CAH) with 17α-hydroxylase/17,20-lyase deficiency is usually characterized by hypertension and primary amenorrhea, sexual infantilism in women, and pseudohermaphroditism in men. hypertension, and sexual infantilism in women
Su Jin Lee +6 more
doaj +1 more source
Composite pheochromocytoma of the adrenal gland: a case series
, 2015 Background: Composite pheochromocytoma is a rare pathological condition characterized by elements of both pheochromocytoma and neurogenic tumors. However, detailed clinical outcomes of this tumor have not been fully shown.
Tsukasa Igawa +13 more
core +1 more source
TRPML3 distribution in salivary gland, adrenal gland, and pituitary gland.
, 2022 (A) Overview image of the salivary gland with its lobules. Two submandibular lymph nodes (LN) are located at the sites. (B) Zoomed image of the upper lmph node (LN). (C) Zoomed image of the salivary gland tissue reveals the typical structure of secretory
Ulrich Boehm (180339) +10 more
core +1 more source
Advanced Science, EarlyView.This study explores the opposing effects of the mGluR2 and mGluR3 receptors on amyloid precursor protein processing. mGluR2 promotes amyloidogenic cleavage, while mGluR3 favors non‐amyloidogenic pathways. Using a brain‐penetrant nanobody as a mGluR2 positive allosteric modulator, the study uncovers how its chronic activation aggravates amyloid‐β burden
Pierre‐André Lafon +21 more
wiley +1 more source
Urology Research and Practice, 2019 Introduction: Renal cell cancer (RCC) represents the fifth most common cancer in men, with a rising incidence. Computerized tomography (CT) remains the most appropriate imaging modality to diagnose renal malignancies.
Aves Editorial Aves Editorial
doaj +2 more sources