The Role of Epigenetics in Type 1 Diabetes

por Jerram, Samuel T., Dang, Mary N., Leslie, R. David
Publicado 2017

Diagnostic challenges and management of a patient with acromegaly due to ectopic growth hormone-releasing hormone secretion from a bronchial carcinoid tumour

por Kyriakakis, Nikolaos, Trouillas, Jacqueline, Dang, Mary N, Lynch, Julie, Belchetz, Paul, Korbonits, Márta, Murray, Robert D
Publicado 2017

Pseudoacromegaly: A Differential Diagnostic Problem for Acromegaly With a Genetic Solution

por Dahlqvist, Per, Spencer, Rupert, Marques, Pedro, Dang, Mary N., Glad, Camilla A.M., Johannsson, Gudmundur, Korbonits, Márta
Publicado 2017

Cantú syndrome with coexisting familial pituitary adenoma

por Marques, Pedro, Spencer, Rupert, Morrison, Patrick J., Carr, Ian M., Dang, Mary N., Bonthron, David T., Hunter, Steven, Korbonits, Márta
Publicado 2018

Risk category system to identify pituitary adenoma patients with AIP mutations

por Caimari, Francisca, Hernández-Ramírez, Laura Cristina, Dang, Mary N, Gabrovska, Plamena, Iacovazzo, Donato, Stals, Karen, Ellard, Sian, Korbonits, Márta
Publicado 2018

Pituitary Carcinoma in a Patient with an SDHB Mutation

por Tufton, Nicola, Roncaroli, Federico, Hadjidemetriou, Irene, Dang, Mary N, Dénes, Judit, Guasti, Leonardo, Thom, Maria, Powell, Michael, Baldeweg, Stephanie E, Fersht, Naomi, Korbonits, Márta
Publicado 2017

Emergence of Pituitary Adenoma in a Child during Surveillance: Clinical Challenges and the Family Members' View in an AIP Mutation-Positive Family

por Marques, Pedro, Barry, Sayka, Ronaldson, Amy, Ogilvie, Arla, Storr, Helen L., Goadsby, Peter J., Powell, Michael, Dang, Mary N., Chahal, Harvinder S., Evanson, Jane, Kumar, Ajith V., Grieve, Joan, Korbonits, Márta
Publicado 2018

MAFA missense mutation causes familial insulinomatosis and diabetes mellitus

por Iacovazzo, Donato, Flanagan, Sarah E., Walker, Emily, Quezado, Rosana, de Sousa Barros, Fernando Antonio, Caswell, Richard, Johnson, Matthew B., Wakeling, Matthew, Brändle, Michael, Guo, Min, Dang, Mary N., Gabrovska, Plamena, Niederle, Bruno, Christ, Emanuel, Jenni, Stefan, Sipos, Bence, Nieser, Maike, Frilling, Andrea, Dhatariya, Ketan, Chanson, Philippe, de Herder, Wouter W., Konukiewitz, Björn, Klöppel, Günter, Stein, Roland, Korbonits, Márta, Ellard, Sian
Publicado 2018

Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study

por Iacovazzo, Donato, Caswell, Richard, Bunce, Benjamin, Jose, Sian, Yuan, Bo, Hernández-Ramírez, Laura C., Kapur, Sonal, Caimari, Francisca, Evanson, Jane, Ferraù, Francesco, Dang, Mary N., Gabrovska, Plamena, Larkin, Sarah J., Ansorge, Olaf, Rodd, Celia, Vance, Mary L., Ramírez-Renteria, Claudia, Mercado, Moisés, Goldstone, Anthony P., Buchfelder, Michael, Burren, Christine P., Gurlek, Alper, Dutta, Pinaki, Choong, Catherine S., Cheetham, Timothy, Trivellin, Giampaolo, Stratakis, Constantine A., Lopes, Maria-Beatriz, Grossman, Ashley B., Trouillas, Jacqueline, Lupski, James R., Ellard, Sian, Sampson, Julian R., Roncaroli, Federico, Korbonits, Márta
Publicado 2016