Pituitary Lesions in Multiple endocrine Neoplasia Syndrome (MENS) Type 1

Author:

Capella C.,Riva C.,Leutner M.,La Rosa S.

Publisher

Elsevier BV

Subject

Cell Biology,Pathology and Forensic Medicine

Reference26 articles.

1. Acromegaly and pituitary adenoma with pheochromocytoma: a variant of multiple endocrine neoplasia;Anderson;Clin Endocrinol,1981

2. Pancreatic endocrine tumor producing growth hormone-releasing hormone associated with multiple endocrine neoplasia type I syndrome;Asa;Acta Endocrinol,1987

3. Familial multiple endocrine adenoma-peptic ulcer complex;Ballard;Medicine,1964

4. The multiple endocrine neoplasia-syndromes: implications for the study of inherited tumors;Baylin;Semin Oncol,1978

5. Pituitary adenomas: a follow-up study of Cushing series;s German;Clin Neurosurg 10: 72 - 81 6 Horvath E, (1988) Pituitary hyperplasia Path Res Pract,1964

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1. Pituitary adenomas in the setting of multiple endocrine neoplasia type 1: a single-institution experience;Journal of Neurosurgery;2021-04

2. Familial Tumor Syndromes;Practical Surgical Neuropathology: A Diagnostic Approach;2018

3. Is Routine Screening of Young Asymptomatic MEN1 Patients Necessary?;World Journal of Surgery;2017-03-20

4. Familial Endocrine Syndromes;Surgical Pathology Clinics;2014-12

5. Familial Pituitary Adenomas;Pituitary Disorders;2013-03-08

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