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期刊名:Endocrinology diabetes and metabolism case reports

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ISSN:2052-0573

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IF/分区:0.7/N/A

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共收录本刊相关文章索引1028
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
Prethivan Pillai Gopalakrishnan,Amit Banerjee,Rachael Milne et al. Prethivan Pillai Gopalakrishnan et al.
Summary: RFX6 maturity-onset diabetes of the young (RFX6-MODY) is a relatively new MODY subtype, with limited guidance on management, particularly in pregnancy. We report the clinical features and management of two female...
Ruixue Sun,Shuang Liu,Hong Han et al. Ruixue Sun et al.
Summary: Iatrogenic Cushing syndrome caused by topical corticosteroid preparations is only reported in infants. We describe a case in a patient with obsessive-compulsive disorder: the patient had tic disorder and obsessiv...
José Luis Paz-Ibarra,Marialejandra Delgado Rojas,Edward Paucar Holgado et al. José Luis Paz-Ibarra et al.
Summary: Papillary thyroid carcinoma (PTC) is the most frequent type of differentiated thyroid cancer, while thyroglossal duct cysts (TGDCs) are common congenital anomalies of the neck. The coexistence of PTC within a TGD...
Yasemin Keskin,Pınar Dağ,Elif Buse Güngör Yasemin Keskin
Summary: This case report describes an 84-year-old male patient who presented with symptoms of intestinal obstruction and was subsequently diagnosed with metastatic adrenocortical carcinoma (ACC), a rare and aggressive en...
Ananda Mohan Chakraborty,Jayaditya Ghosh,Liza Das et al. Ananda Mohan Chakraborty et al.
Summary: Medullary thyroid carcinoma (MTC) constitutes 5-10% of thyroid malignancies but accounts for 15% of thyroid cancer-related mortality. Twenty percent of MTC are hereditary and are part of familial MTC or multiple ...
Juveria Javid,Sumana Reddy Kunnuru,Beatrice Anne et al. Juveria Javid et al.
Summary: This case report describes a 55-year-old postmenopausal woman who presented with Cushingoid features and progressive weight gain over a year. Evaluation revealed low basal cortisol levels and a suboptimal respons...
Leo L T Meller,Ghassan Akkad,Mary Patterson Leo L T Meller
Summary: Panhypopituitarism, characterized by multiple pituitary hormone deficiencies, is most often diagnosed in infancy or early childhood with adolescent presentation being uncommon. We present a 12-year-old female wit...
Aparajita Roy,Kieran Mullins Aparajita Roy
Summary: Apparent mineralocorticoid excess (AME) syndrome is a rare condition caused by the inhibition of the renal enzyme 11β-hydroxysteroid dehydrogenase type 2 (11β-HSD2). The most common acquired cause is chronic li...
Annabelle G Hayes,Morton G Burt Annabelle G Hayes
Summary: Small clinically silent phaeochromocytoma (PCC) can be identified in modern clinical practice as apparent adrenal incidentaloma or during screening of patients with familial tumour syndromes. Composite tumours co...
Shingo Murasawa,Fumiya Isozaki,Shinobu Takayasu et al. Shingo Murasawa et al.
Summary: A 70-year-old woman with Hashimoto thyroiditis, treated with levothyroxine, was diagnosed with rheumatoid arthritis 1 year prior and subsequently began methotrexate (MTX) therapy. She presented with a 2-week hist...