Results 161 to 170 of about 3,490 (181)
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Assessment of the Role of p27Kip1 Gene in MEN2 and MEN2-Related Syndromes

2011
Tomoko Sekiya   +3 more
openaire   +1 more source

Multiple Endocrine Neoplasia Type 2 (MEN2)

Encyclopedia of Pathology, 2022
Özgür Mete, Sara Pakbaz
exaly  

Impact of gastrointestinal symptoms on quality of life in MEN2

Clinical Endocrinology, 2021
Mariia Goncharova, Maralyn Druce
exaly  

Mutational spectrum of MEN1 and MEN2 syndrome in Croatian patients

European journal of human genetics
Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome caused by mutations in MEN1 gene. One of its main hallmarks is endocrine and non-endocrine tumor growth (parathyroid tumors, pituitary tumors, gastrinomas, insulinomas, cutaneous tumors, etc.).
Caban, Domagoj   +6 more
openaire  

Phenotypic and genotypic characteristics of patients with MEN2 in france: preliminary features from the MEN2 french database

Endocrine Abstracts
Nicolas Sahakian   +8 more
openaire   +1 more source

Multiple Endocrine Neoplasia Type 2 (MEN2)

2020
Anjelica Hodgson   +2 more
openaire   +1 more source

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