Recent advances in central congenital hypothyroidism

por Schoenmakers, Nadia, Alatzoglou, Kyriaki S, Chatterjee, V Krishna, Dattani, Mehul T
Publicado 2015

SUN-546 Coexistent Resistance to Thyroid Hormone Beta and Viral Thyroiditis

por Golubic, Rajna, Kakad, Rakhi, Chatterjee, V Krishna, Moran, Carla
Publicado 2019

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism

por Aycan, Zehra, Cangul, Hakan, Muzza, Marina, Bas, Veysel N., Fugazzola, Laura, Chatterjee, V. Krishna, Persani, Luca, Schoenmakers, Nadia
Publicado 2017

OR26-06 Cardiovascular Morbidity And Mortality In Patients With Resistance to THYROID Hormone (RTH): A Linked Record Study

por Okosieme, Onyebuchi, Usman, Danyal, Taylor, Peter, Dayan, Colin, Lyons, Greta, Moran, Carla M, Chatterjee, V Krishna K, Rees, Aled
Publicado 2023

Insight Into Molecular Determinants of T3 vs T4 Recognition From Mutations in Thyroid Hormone Receptor α and β

por Wejaphikul, Karn, Groeneweg, Stefan, Hilhorst-Hofstee, Yvonne, Chatterjee, V Krishna, Peeters, Robin P, Meima, Marcel E, Visser, W Edward
Publicado 2019

Adult-onset hyperinsulinaemic hypoglycaemia in clinical practice: diagnosis, aetiology and management

por Challis, Benjamin G, Powlson, Andrew S, Casey, Ruth T, Pearson, Carla, Lam, Brian Y, Ma, Marcella, Pitfield, Deborah, Yeo, Giles S H, Godfrey, Edmund, Cheow, Heok K, Chatterjee, V Krishna, Carroll, Nicholas R, Shaw, Ashley, Buscombe, John R, Simpson, Helen L
Publicado 2017

Partial lipodystrophy and insulin resistant diabetes in a patient with a homozygous nonsense mutation in CIDEC

por Rubio-Cabezas, Oscar, Puri, Vishwajeet, Murano, Incoronata, Saudek, Vladimir, Semple, Robert K, Dash, Satya, Hyden, Caroline S S, Bottomley, William, Vigouroux, Corinne, Magré, Jocelyne, Raymond-Barker, Philippa, Murgatroyd, Peter R, Chawla, Anil, Skepper, Jeremy N, Chatterjee, V Krishna, Suliman, Sara, Patch, Ann-Marie, Agarwal, Anil K, Garg, Abhimanyu, Barroso, Inês, Cinti, Saverio, Czech, Michael P, Argente, Jesús, O'Rahilly, Stephen, Savage, David B
Publicado 2009

Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

por Nicholas, Adeline K., Serra, Eva G., Cangul, Hakan, Alyaarubi, Saif, Ullah, Irfan, Schoenmakers, Erik, Deeb, Asma, Habeb, Abdelhadi M., Almaghamsi, Mohammad, Peters, Catherine, Nathwani, Nisha, Aycan, Zehra, Saglam, Halil, Bober, Ece, Dattani, Mehul, Shenoy, Savitha, Murray, Philip G., Babiker, Amir, Willemsen, Ruben, Thankamony, Ajay, Lyons, Greta, Irwin, Rachael, Padidela, Raja, Tharian, Kavitha, Davies, Justin H., Puthi, Vijith, Park, Soo-Mi, Massoud, Ahmed F., Gregory, John W., Albanese, Assunta, Pease-Gevers, Evelien, Martin, Howard, Brugger, Kim, Maher, Eamonn R., Chatterjee, V. Krishna K., Anderson, Carl A., Schoenmakers, Nadia
Publicado 2016