Associated Papers
Multiple endocrine neoplasia type 1 with neuroglycopenic symptoms with a novel heterozygous MEN1 gene mutation.
Jiang X et al.
World Journal of Surgical Oncology, 2025
Alternative splicing generates isoform diversity in MEN1.
Ramachandran A et al.
Endocrine Oncology (bristol, England), 2024
39649118 (PubMed )
Supplement: supplementary_table_3.xlsx › Supplementary_Table_3
Novel MEN1-associated retroperitoneal pleomorphic liposarcoma.
McNicoll CF et al.
Rare Tumors, 2024
Management and Long-Term Follow-Up of Hyperparathyroidism in Multiple Endocrine Neoplasia Type 1: Single Center Experience.
Yavropoulou MP et al.
Journal of Clinical Medicine, 2022
Late onset asymptomatic pancreatic neuroendocrine tumor - A case report on the phenotypic expansion for MEN1.
Kaiwar C et al.
Hereditary Cancer in Clinical Practice, 2017
A patient with novel mutations causing MEN1 and hereditary multiple osteochondroma.
Remde H et al.
Endocrinology, Diabetes & Metabolism Case Reports, 2015
Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.
Dwight T et al.
Clinical Endocrinology, 2000
Adrenal Liposarcoma: A Novel Presentation of Multiple Endocrine Neoplasia Type 1.
Duro T et al.
Aace Clinical Case Reports, 0
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