Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study

OBJECTIVE: Multiple endocrine neoplasia type 2A (MEN 2A) is a rare syndrome caused by RET germline mutations and has been associated with primary hyperparathyroidism (PHPT) in up to 30% of cases. Recommendations on RET screening in patients with apparently sporadic PHPT are unclear. We aimed to esti...

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Detalles Bibliográficos
Autores principales: Larsen, Louise Vølund, Mirebeau-Prunier, Delphine, Imai, Tsuneo, Alvarez-Escola, Cristina, Hasse-Lazar, Kornelia, Censi, Simona, Castroneves, Luciana A, Sakurai, Akihiro, Kihara, Minoru, Horiuchi, Kiyomi, Barbu, Véronique Dorine, Borson-Chazot, Francoise, Gimenez-Roqueplo, Anne-Paule, Pigny, Pascal, Pinson, Stephane, Wohllk, Nelson, Eng, Charis, Aydogan, Berna Imge, Saranath, Dhananjaya, Dvorakova, Sarka, Castinetti, Frederic, Patocs, Attila, Bergant, Damijan, Links, Thera P, Peczkowska, Mariola, Hoff, Ana O, Mian, Caterina, Dwight, Trisha, Jarzab, Barbara, Neumann, Hartmut P H, Robledo, Mercedes, Uchino, Shinya, Barlier, Anne, Godballe, Christian, Mathiesen, Jes Sloth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354718/
https://www.ncbi.nlm.nih.gov/pubmed/32375120
http://dx.doi.org/10.1530/EC-20-0163

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354718/
https://www.ncbi.nlm.nih.gov/pubmed/32375120
http://dx.doi.org/10.1530/EC-20-0163

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