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Diagnostic challenges and management of a patient with acromegaly due to ectopic growth hormone-releasing hormone secretion from a bronchial carcinoid tumour

A male patient presented at the age of 30 with classic clinical features of acromegaly and was found to have elevated growth hormone levels, not suppressing during an oral glucose tolerance test. His acromegaly was originally considered to be of pituitary origin, based on a CT scan, which was interp...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
الحاوية / القاعدة:Endocrinol Diabetes Metab Case Rep
المؤلفون الرئيسيون: Kyriakakis, Nikolaos, Trouillas, Jacqueline, Dang, Mary N, Lynch, Julie, Belchetz, Paul, Korbonits, Márta, Murray, Robert D
التنسيق: Artigo
اللغة:Inglês
منشور في: Bioscientifica Ltd 2017
الموضوعات:
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC5292981/
https://ncbi.nlm.nih.gov/pubmed/28203372
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-16-0104
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