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期刊名:Aace clinical case reports

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ISSN:2376-0605

e-ISSN:2376-0605

IF/分区:1.2/Q4

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共收录本刊相关文章索引543
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
George A Stamatiades,Justin B Echouffo-Tcheugui,Jeffrey R Garber George A Stamatiades
Objective: To demonstrate important points regarding the possible hypoglycemic effects of sulfasalazine and suggest possible underlying mechanism(s) accounting for sulfasalazine-induced hypoglycemia. Methods: We describe a case of reversibl...
Sushma Kadiyala,Yasmin Khan,Valeria de Miguel et al. Sushma Kadiyala et al.
Objective: Succinate dehydrogenase complex, subunit D (SDHD) gene mutations are most commonly associated with head and neck paragangliomas. We describe a pair of cases with early-onset, bilateral pheochromocytoma (PCC) an...
Gael Charbonne,Fatima Hallak,Alma Elizabeth Rivera Cruz et al. Gael Charbonne et al.
Background/objective: Disseminated thyroid autonomy (DTA) and seronegative Graves' disease are rare causes of hyperthyroidism with similar clinical presentations. This case report highlights the diagnostic challenges betw...
Joselyn Tessa Tonleu,Nicolas A Reyes,Natalie D Hillerson et al. Joselyn Tessa Tonleu et al.
Background/objective: Glycogenic hepatopathy is characterized by diffuse glycogen accumulation in hepatocytes that leads to hepatomegaly and elevated transaminases. Notably, the condition is reversible as improving glycem...
Hye Jeong Han,Jacob Moalem,Angela R Shih et al. Hye Jeong Han et al.
Background/objective: Multiple endocrine neoplasia 4 (MEN4) is a rare syndrome caused by germline mutations in CKDN1B, and it shares clinical manifestations with MEN1, including primary hyperparathyroidism, pituitary aden...
Talita Fischer Oliveira,Humberto Batista Ferreira,Luís Henrique Dias Lima et al. Talita Fischer Oliveira et al.
Background: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder characterized by the occurrence of combined tumors in different glands, usually the parathyroid, pancreas and pituitary, as well...
Bailey N Johnson,Signe Braafladt,John-Paul Lavik et al. Bailey N Johnson et al.
Background/objective: Increased utilization of cross-sectional imaging has led to a rise in diagnosis of incidental adrenal lesions. Physicians in many clinical settings are increasingly faced with addressing these incide...
Sanghwa E Park,Thanh D Hoang,Derek J Stocker et al. Sanghwa E Park et al.
Background/objective: Gallium-68 DOTATATE (68Ga-DOTATATE) positron emission tomography/computed tomography (CT) is a somatostatin receptor (SSTR)-based imaging with high sensitivity that can be used for detection of pheoc...
Gayatri Jaiswal,Fnu Varsha,Patricia Bononi et al. Gayatri Jaiswal et al.
Background/objective: A 58-year-old postmenopausal woman presented with polycythemia on routine laboratory examinations along with long-standing hirsutism. The objective of this report is to highlight polycythemia as a ra...
Samuel Amankwah,Maria Luzuriaga,Krista Denning et al. Samuel Amankwah et al.
Background/objective: We present a case of a woman with persistent abdominal pain, leading to the discovery of a rare solitary fibrous tumor (SFT) in the adrenal gland. The rarity of adrenal SFTs and their diagnostic chal...