Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism von Aycan, Zehra, Cangul, Hakan, Muzza, Marina, Bas, Veysel N, Fugazzola, Laura, Chatterjee, V Krishna, Persani, Luca, Schoenmakers, Nadia

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Recent advances in central congenital hypothyroidism von Schoenmakers, Nadia, Alatzoglou, Kyriaki S, Chatterjee, V Krishna, Dattani, Mehul T

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Prevalence and Relative Risk of Other Autoimmune Diseases in Subjects with Autoimmune Thyroid Disease von Boelaert, Kristien, PhD, Newby, Paul R, Simmonds, Matthew J., PhD, Holder, Roger L, Carr-Smith, Jacqueline D, Heward, Joanne M., PhD, Manji, Nilusha, Allahabadia, Amit, MD, Armitage, Mary, DM, Chatterjee, Krishna V., PhD, Lazarus, John H., MD, Pearce, Simon H., PhD, Vaidya, Bijay, PhD, Gough, Stephen C., PhD, Franklyn, Jayne A., PhD

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

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Glucocorticoid replacement therapy and pharmacogenetics in Addison's disease: effects on bone von Løvås, Kristian, Gjesdal, Clara G, Christensen, Monika, Wolff, Anette B, Almås, Bjørg, Svartberg, Johan, Fougner, Kristian J, Syversen, Unni, Bollerslev, Jens, Falch, Jan A, Hunt, Penelope J, Chatterjee, V Krishna K, Husebye, Eystein S

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Long-Term DHEA Replacement in Primary Adrenal Insufficiency: A Randomized, Controlled Trial von Gurnell, Eleanor M., Hunt, Penelope J., Curran, Suzanne E., Conway, Catherine L., Pullenayegum, Eleanor M., Huppert, Felicia A., Compston, Juliet E., Herbert, Joseph, Chatterjee, V. Krishna K.

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Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community von Cangul, Hakan, Aycan, Zehra, Olivera-Nappa, Alvaro, Saglam, Halil, Schoenmakers, Nadia A., Boelaert, Kristien, Cetinkaya, Semra, Tarim, Omer, Bober, Ece, Darendeliler, Feyza, Bas, Veysel, Demir, Korcan, Aydin, Banu K., Kendall, Michaela, Cole, Trevor, Högler, Wolfgang, Chatterjee, V. Krishna K., Barrett, Timothy G., Maher, Eamonn R.

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Quality of Life in European Patients with Addison's Disease: Validity of the Disease-Specific Questionnaire AddiQoL von Øksnes, Marianne, Bensing, Sophie, Hulting, Anna-Lena, Kämpe, Olle, Hackemann, Annika, Meyer, Gesine, Badenhoop, Klaus, Betterle, Corrado, Parolo, Anna, Giordano, Roberta, Falorni, Alberto, Papierska, Lucyna, Jeske, Wojciech, Kasperlik-Zaluska, Anna A, Chatterjee, V. Krishna K, Husebye, Eystein S, Løvås, Kristian

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Human Metabolic Syndrome Resulting From Dominant-Negative Mutations in the Nuclear Receptor Peroxisome Proliferator-Activated Receptor-γ von SAVAGE, David B, TAN, Garry D, DIXON, Adrian K, DUNNE, Fidelma, BOIANI, Romina, CINTI, Saverio, VIDAL-PUIG, Antonio, KARPE, Fredrik, CHATTERJEE, V. Krishna K, O'RAHILLY, Stephen, ACERINI, Carlo L, JEBB, Susan A, AGOSTINI, Maura, GURNELL, Mark, WILLIAMS, Rachel L, UMPLEBY, A. Margot, THOMAS, E. Louise, BELL, Jimmy D

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Development of a Disease-Specific Quality of Life Questionnaire in Addison’s Disease von Løvås, Kristian, Curran, Suzanne, Øksnes, Marianne, Husebye, Eystein S, Huppert, Felicia A, Chatterjee, V. Krishna K

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Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism von Cangul, Hakan, Liao, Xiao-Hui, Schoenmakers, Erik, Kero, Jukka, Barone, Sharon, Srichomkwun, Panudda, Iwayama, Hideyuki, Serra, Eva G, Saglam, Halil, Eren, Erdal, Tarim, Omer, Nicholas, Adeline K, Zvetkova, Ilona, Anderson, Carl A, Frankl, Fiona E Karet, Boelaert, Kristien, Ojaniemi, Marja, Jääskeläinen, Jarmo, Patyra, Konrad, Löf, Christoffer, Williams, E Dillwyn, Soleimani, Manoocher, Barrett, Timothy, Maher, Eamonn R, Chatterjee, V Krishna, Refetoff, Samuel, Schoenmakers, Nadia

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A dynamic mechanism of nuclear receptor activation and its perturbation in a human disease von Schwabe, John W. R, Kallenberger, Bettina C, Love, James D, Chatterjee, V. Krishna K

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Leptin Deficiency Unmasks the Deleterious Effects of Impaired Peroxisome Proliferator–Activated Receptor γ Function (P465L PPARγ) in Mice von Gray, Sarah L, Nora, Edoardo Dalla, Grosse, Johannes, Manieri, Monia, Stoeger, Tobias, Medina-Gomez, Gema, Burling, Keith, Wattler, Sigrid, Russ, Andreas, Yeo, Giles S.H, Chatterjee, V. Krishna, O'Rahilly, Stephen, Voshol, Peter J, Cinti, Saverio, Vidal-Puig, Antonio

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Pulsed monoclonal antibody treatment and autoimmune thyroid disease in multiple sclerosis von Coles, Alasdair J, Wing, Mark, Smith, Sheila, Coraddu, Francesca, Greer, Sandra, Taylor, Craig, Weetman, Anthony, Hale, Geoff, Chatterjee, V Krishna, Waldmann, Herman, Compston, Alastair

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PPAR gamma and human metabolic disease von Semple, Robert K, Chatterjee, V Krishna K, O'Rahilly, Stephen

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Maternal Isodisomy for Chromosome 9 Causing Homozygosity for a Novel FOXE1 Mutation in Syndromic Congenital Hypothyroidism von Castanet, Mireille, Mallya, Uma, Agostini, Maura, Schoenmakers, Erik, Mitchell, Catherine, Demuth, Stephanie, Raymond, F. Lucy, Schwabe, John, Gurnell, Mark, Chatterjee, V. Krishna

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PPARγ Agonists Ameliorate Endothelial Cell Activation via Inhibition of Diacylglycerol–Protein Kinase C Signaling Pathway: Role of Diacylglycerol Kinase von Verrier, Emily, Wang, Lijun, Wadham, Carol, Albanese, Nathaniel, Hahn, Chris, Gamble, Jennifer R, Chatterjee, V Krishna K, Vadas, Mathew A, Xia, Pu

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Insight Into Molecular Determinants of T3 vs T4 Recognition From Mutations in Thyroid Hormone Receptor α and β von Wejaphikul, Karn, Groeneweg, Stefan, Hilhorst-Hofstee, Yvonne, Chatterjee, V Krishna, Peeters, Robin P, Meima, Marcel E, Visser, W Edward

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Liver X receptor inhibition potentiates mitotane-induced adrenotoxicity in ACC von Warde, Kate M, Schoenmakers, Erik, Ribes Martinez, Eduardo, Lim, Yi Jan, Leonard, Maeve, Lawless, Sarah J, O’Shea, Paula, Chatterjee, Krishna V, Gurnell, Mark, Hantel, Constanze, Dennedy, Michael Conall

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Digenic inheritance of severe insulin resistance in a human pedigree von O'Rahilly, Stephen, Savage, David B, Agostini, Maura, Barroso, Inês, Gurnell, Mark, Luan, Jian'an, Meirhaeghe, Aline, Harding, Anne-Helen, Ihrke, Gudrun, Rajanayagam, Odelia, Soos, Maria A, George, Stella, Berger, Dirk, Thomas, E. Louise, Bell, Jimmy D, Meeran, Karim, Ross, Richard J, Vidal-Puig, Antonio, Wareham, Nicholas J, Chatterjee, V. Krishna K, Schafer, Alan J

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