Results 31 to 40 of about 145,553 (265)
Clinical Case Reports, 2023 Key Clinical Message Parathyroid lipoadenoma is a rare type of parathyroid adenoma, described as a single parathyroid adenoma with more than 50% fat on histologic examination and an unknown etiology, which is one of the rare causes of primary ...
Yihan Wang, Yan Chen, Yantao Fu
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Clonal Composition of Human Adrenocortical Neoplasms [PDF]
, 1994 The mechanisms of tumorigenesis of adrenocortical neoplasms are still not understood. Tumor formation may be the result of spontaneous transformation of adrenocortical cells by somatic mutations.
Travis, W. +7 more
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Frontiers in Endocrinology, 2018 Thyroid tumors usually present as masses in the thyroid gland. While the majority of these tumors represent neoplasms of thyroid tissues, mainly of follicular epithelial cell differentiation, the differential diagnosis includes other lesions, such as C ...
Sylvia L. Asa +3 more
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International Archives of Otorhinolaryngology, 2018 Introduction Intraoperative parathyroid hormone (ioPTH) testing is a widely accepted standard for assessing the parathyroid gland function. A decline of preoperative parathyroid hormone (PTH) levels by more than 50% is one accepted measure of parathyroid
Maheer M. Masood, Trevor G. Hackman
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, 2021 Parathyroid neoplasms show a wide spec- trum of morphology (adenoma-carcinoma), which is difficult to predict biological behaviour by histomorphology. The aim of this study is to evaluate morphological and immunohistochemical predictors of biologi- cal ...
Üner, Halit +2 more
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Current Knowledge on Atypical Parathyroid Tumors and Emerging Strategies for Risk Stratification [PDF]
Endocrinology and MetabolismAtypical parathyroid tumors (APTs) are an uncommon subset of parathyroid neoplasms that carry substantial clinical relevance because of their histological and clinical resemblance to parathyroid cancer.
Hye-Sun Park +4 more
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A late diagnosis of MEN 1 Syndrome in a young patient initially pre-senting with nephrolithiasis
Liječnički vjesnik, 2023 Multiple Endocrine Neoplasms Type 1 (MEN 1), originally called Wermer Syndrome, is a rare hereditary condition caused by mutations in the MEN1 tumor suppressor gene.
Ana Čala, Tina Dušek
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Epigenetic Activation of SOX11 in Lymphoid Neoplasms by Histone Modifications [PDF]
, 2011 Recent studies have shown aberrant expression of SOX11 in various types of aggressive B-cell neoplasms. To elucidate the molecular mechanisms leading to such deregulation, we performed a comprehensive SOX11 gene expression and epigenetic study in stem ...
Amador Virginia +107 more
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Advanced Science, EarlyView.Klotho deficiency promotes podocyte mitochondrial dysfunction and ferroptosis through activation of the PKCα/CUX1/SPARC/TGFβ‐RII axis. SPARC emerges as a key mediator linking Klotho loss to podocyte injury in DKD and other kidney injury models, suggesting broader implications for CKD progression.
Qing Yang +11 more
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Endokrynologia PolskaINTRODUCTION: Primary hyperparathyroidism (PHPT) is caused by excessive hormone secretion from one or more parathyroid glands. Based on their morphological and immunophenotypic characteristics, parathyroid glands can be considered as neuroendocrine ...
Dorota Anna Brodowska-Kania +11 more
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