Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment von Hwang, Jessica L., Weiss, Roy E.

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A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up von Grogan, Raymon H., MD, Kaplan, Sharone P., MSW, Cao, Hongyuan, PhD, Weiss, Roy E., MD, PhD, DeGroot, Leslie J., MD, Simon, Cassie A., CTR, Embia, Omran M.A., MBChB, Angelos, Peter, MD, PhD, Kaplan, Edwin L., MD, Schechter, Rebecca B., MD

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American Thyroid Association Guide to Investigating Thyroid Hormone Economy and Action in Rodent and Cell Models von Bianco, Antonio C., Anderson, Grant, Forrest, Douglas, Galton, Valerie Anne, Gereben, Balázs, Kim, Brian W., Kopp, Peter A., Liao, Xiao Hui, Obregon, Maria Jesus, Peeters, Robin P., Refetoff, Samuel, Sharlin, David S., Simonides, Warner S., Weiss, Roy E., Williams, Graham R.

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Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency von Verge, Charles F, Konrad, Daniel, Cohen, Michal, Di Cosmo, Caterina, Dumitrescu, Alexandra M, Marcinkowski, Teresa, Hameed, Shihab, Hamilton, Jill, Weiss, Roy E, Refetoff, Samuel

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Tissue-Specific Thyroid Hormone Deprivation and Excess in Monocarboxylate Transporter (Mct) 8-Deficient Mice von Dumitrescu, Alexandra M, Liao, Xiao-Hui, Weiss, Roy E, Millen, Kathleen, Refetoff, Samuel

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Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Mono... von Iwayama, Hideyuki, Kakita, Hiroki, Iwasa, Masumi, Adachi, Shinsuke, Takano, Kyoko, Kikuchi, Masahiro, Fujisawa, Yasuko, Osaka, Hitoshi, Yamada, Yasumasa, Okumura, Akihisa, Hirani, Khemraj, Weiss, Roy E, Refetoff, Samuel

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Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation von Refetoff, Samuel, Pappa, Theodora, Williams, Meredith K, Matheus, M Gisele, Liao, Xiao-Hui, Hansen, Karen, Nicol, Lindsey, Pierce, Melinda, Blasco, Peter A, Wiebers Jensen, Mandie, Bernal, Juan, Weiss, Roy E, Dumitrescu, Alexandra M, LaFranchi, Stephen

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Changes in Thyroid Status During Perinatal Development of MCT8-Deficient Male Mice von Ferrara, Alfonso Massimiliano, Liao, Xiao-Hui, Gil-Ibáñez, Pilar, Marcinkowski, Teresa, Bernal, Juan, Weiss, Roy E, Dumitrescu, Alexandra M, Refetoff, Samuel

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Adeno Associated Virus 9–Based Gene Therapy Delivers a Functional Monocarboxylate Transporter 8, Improving Thyroid Hormone Availability to the Brain of Mct8-Deficient Mice von Iwayama, Hideyuki, Liao, Xiao-Hui, Braun, Lyndsey, Bárez-López, Soledad, Kaspar, Brian, Weiss, Roy E., Dumitrescu, Alexandra M., Guadaño-Ferraz, Ana, Refetoff, Samuel

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Mutations in SECISBP2 result in abnormal thyroid hormone metabolism von Dumitrescu, Alexandra M, Liao, Xiao-Hui, Abdullah, Mohamed S Y, Lado-Abeal, Joaquin, Majed, Fathia Abdul, Moeller, Lars C, Boran, Gerard, Schomburg, Lutz, Weiss, Roy E, Refetoff, Samuel

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Clinical and Molecular Characterization of a Novel Selenocysteine Insertion Sequence-Binding Protein 2 (SBP2) Gene Mutation (R128X) von Di Cosmo, Caterina, McLellan, Neil, Liao, Xiao-Hui, Khanna, Kum Kum, Weiss, Roy E., Papp, Laura, Refetoff, Samuel

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Classification and Proposed Nomenclature for Inherited Defects of Thyroid Hormone Action, Cell Transport, and Metabolism von Refetoff, Samuel, Bassett, J.H. Duncan, Beck-Peccoz, Paolo, Bernal, Juan, Brent, Gregory, Chatterjee, Krishna, De Groot, Leslie J., Dumitrescu, Alexandra M., Jameson, J. Larry, Kopp, Peter A., Murata, Yoshiharu, Persani, Luca, Samarut, Jacques, Weiss, Roy E., Williams, Graham R., Yen, Paul M.

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Combined Use of RT-qPCR and NGS for Identification and Surveillance of SARS-CoV-2 Variants of Concern in Residual Clinical Laboratory Samples in Miami-Dade County, Florida von Carattini, Yamina L, Griswold, Anthony, Williams, Sion, Valiathan, Ranjini, Zhou, Yi, Shukla, Bhavarth, Abbo, Lilian M, Parra, Katiuska, Jorda, Merce, Nimer, Stephen D, Sologon, Corneliu, Gallegos, Hilma R, Weiss, Roy E, Ferreira, Tanira, Memon, Abdul, Paige, Peter G, Thomas, Emmanuel, Andrews, David M

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Classification and Proposed Nomenclature for Inherited Defects of Thyroid Hormone Action, Cell Transport, and Metabolism von Refetoff, Samuel, Bassett, J. H. Duncan, Beck-Peccoz, Paolo, Bernal, Juan, Brent, Gregory, Chatterjee, Krishna, De Groot, Leslie J, Dumitrescu, Alexandra M, Jameson, J. Larry, Kopp, Peter A, Murata, Yoshiharu, Persani, Luca, Samarut, Jacques, Weiss, Roy E, Williams, Graham R, Yen, Paul M

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The Nuclear Receptor Corepressor (NCoR) Controls Thyroid Hormone Sensitivity and the Set Point of the Hypothalamic-Pituitary-Thyroid Axis von Astapova, Inna, Vella, Kristen R, Ramadoss, Preeti, Holtz, Kaila A, Rodwin, Benjamin A, Liao, Xiao-Hui, Weiss, Roy E, Rosenberg, Michael A, Rosenzweig, Anthony, Hollenberg, Anthony N

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Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ von Ebrhim, Reham S., Bruellman, Ryan J., Watanabe, Yui, Creech, Matthew K., Abdullah, Mohamed A., Dumitrescu, Alexandra M., Refetoff, Samuel, Weiss, Roy E.

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Distinct Roles of Deiodinases on the Phenotype of Mct8 Defect: A Comparison of Eight Different Mouse Genotypes von Liao, Xiao-Hui, Di Cosmo, Caterina, Dumitrescu, Alexandra M, Hernandez, Arturo, Van Sande, Jacqueline, St. Germain, Donald L, Weiss, Roy E, Galton, Valerie Anne, Refetoff, Samuel

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Thyroid Hormone Excess Rather Than Thyrotropin Deficiency Induces Osteoporosis in Hyperthyroidism von Bassett, J. H. Duncan, O’Shea, Patrick J, Sriskantharajah, Srividya, Rabier, Bénédicte, Boyde, Alan, Howell, Peter G. T, Weiss, Roy E, Roux, Jean-Paul, Malaval, Luc, Clement-Lacroix, Phillipe, Samarut, Jacques, Chassande, Olivier, Williams, Graham R

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Effect of Pioglitazone on Adrenocorticotropic Hormone and Cortisol Secretion in Cushing’s Disease von Suri, Daesman, Weiss, Roy E.

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Role of type 2 deiodinase in response to acute lung injury (ALI) in mice von Barca-Mayo, Olga, Liao, Xiao-Hui, DiCosmo, Caterina, Dumitrescu, Alexandra, Moreno-Vinasco, Liliana, Wade, Michael S, Sammani, Saad, Mirzapoiazova, Tamara, Garcia, Joe G. N, Refetoff, Samuel, Weiss, Roy E

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