Thyroid disorders in subfertility and early pregnancy

por Anandappa, Samantha, Joshi, Mamta, Polanski, Lukasz, Carroll, Paul V.
Publicado 2020

Pituitary apoplexy: two very different presentations with one unifying diagnosis

por Harris, Sophie M, Cannon, John E, Carroll, Paul V, Thomas, Stephen M
Publicado 2010

Glucocorticoid management of adrenal insufficiency in the United Kingdom: assessment using real-world data

por Iqbal, Kamran, Halsby, Kate, Murray, Robert D, Carroll, Paul V, Petermann, Robert
Publicado 2018

Making (mis) sense of asymptomatic marked hypercalcemia in pregnancy

por Maltese, Giuseppe, Izatt, Louise, McGowan, Barbara M., Hafeez, Kashif, Hubbard, Johnathan G., Carroll, Paul V.
Publicado 2017

MON-924 Susceptibility Genetic Testing and Functional Imaging Modalities in the Management of Bladder Paragangliomas

por Anandappa, Samantha, Joshi, Mamta, Breen, Louise A, Thurairaja, Ramesh, Christodoulou, Dimitra, Jacques, Audrey, McGowan, Barbara Maria Cristina, Izatt, Louise, Velusamy, Anand, Carroll, Paul V
Publicado 2020

Simultaneous Kidney and Parathyroid Transplantation in the Management of Genetic Hypoparathyroidism in a Child

por Vallant, Natalie, Sinha, Manish D., Cheung, Moira, Ware, Nick, Jones, Helen, Buck, Jackie, Boffa, Catherine, Irving, Melita, Carroll, Paul V., Hubbard, Johnathan, Gökmen, Refik, Rees, Lesley, Gogalniceanu, Petrut, Kessaris, Nicos
Publicado 2022

Tumour detection and outcomes of surveillance screening in SDHB and SDHD pathogenic variant carriers

por White, Gemma, Velusamy, Anand, Anandappa, Samantha, Masucci, Michael, Breen, Louise A, Joshi, Mamta, McGowan, Barbara, Hubbard, Johnathan G H, Obholzer, Rupert, Christodoulou, Dimitra, Jacques, Audrey, Touska, Philip, Hassan, Fahim-Ul, Izatt, Louise, Carroll, Paul V
Publicado 2022

Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients

por Arlt, Wiebke, Willis, Debbie S., Wild, Sarah H., Krone, Nils, Doherty, Emma J., Hahner, Stefanie, Han, Thang S., Carroll, Paul V., Conway, Gerry S., Rees, D. Aled, Stimson, Roland H., Walker, Brian R., Connell, John M. C., Ross, Richard J.
Publicado 2010

Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperpl...

por Krone, Nils, Rose, Ian T., Willis, Debbie S., Hodson, James, Wild, Sarah H., Doherty, Emma J., Hahner, Stefanie, Parajes, Silvia, Stimson, Roland H., Han, Thang S., Carroll, Paul V., Conway, Gerry S., Walker, Brian R., MacDonald, Fiona, Ross, Richard J., Arlt, Wiebke
Publicado 2013

Investigating the role of somatic sequencing platforms for phaeochromocytoma and paraganglioma in a large UK cohort

por Winzeler, Bettina, Tufton, Nicola, S. Lim, Eugenie, Challis, Ben G., Park, Soo‐Mi, Izatt, Louise, Carroll, Paul V., Velusamy, Anand, Hulse, Tony, Whitelaw, Benjamin C., Martin, Ezequiel, Rodger, Fay, Maranian, Melanie, Clark, Graeme R., A. Akker, Scott, Maher, Eamonn R., Casey, Ruth T.
Publicado 2021