11 مهر 1402
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مرکز تحقیقات غدد و متابولیسم پژوهشگاه علوم غدد و متابولیسم

دانشگاه علوم پزشکی

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Medical management of pancreatic neuroendocrine tumors in patients with MEN 1: case report
neuroendocrine

Medical management of pancreatic neuroendocrine tumors in patients with MEN 1: case report

Multiple endocrine neoplasia type 1 (MEN-1) is a rare inherited autosomal dominant disease which manifests itself with at least one clinical scenario before 45 years of age. The value of somatostatin analogue therapy is unknown in the treatment of non-functioning pancreatic tumours and a few studies have been published in this field

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