Induction of lactation in a patient with complete androgen insensitivity syndrome

por Voon, Kimberly, Stuckey, Bronwyn G A
Publicado 2023

Digenic Congenital Hypogonadotropic Hypogonadism Due to Heterozygous GNRH1 p.R31C and AMHR2 p.G445_L453del Variants

por Stuckey, Bronwyn G. A., Jones, Timothy W., Ward, Bryan K., Wilson, Scott G.
Publicado 2023

Congenital hypogonadotrophic hypogonadism, induction of minipuberty, and future fertility

por Stuckey, Bronwyn G A, Nolan, James D, Hurley, David M, Martin, Graeme B
Publicado 2023

Serum 21-Deoxycortisol for Diagnosis of Nonclassic Congenital Adrenal Hyperplasia in Women With Androgen Excess

por Ng, Jennifer L, Lim, Ee Mun, Zhang, Rui, Beilby, John P, Watts, Gerald F, Brown, Suzanne J, Stuckey, Bronwyn G A
Publicado 2023

Hemodynamic Effects of Fenofibrate and Coenzyme Q(10) in Type 2 Diabetic Subjects With Left Ventricular Diastolic Dysfunction

por Chew, Gerard T., Watts, Gerald F., Davis, Timothy M.E., Stuckey, Bronwyn G.A., Beilin, Lawrence J., Thompson, Peter L., Burke, Valerie, Currie, Philip J.
Publicado 2008

FRI434 Long-term Self-reported Outcomes Of Randomized Testosterone (T) vs Placebo (P) Treatment In The T4DM Study

por Handelsman, David J, Grossmann, Mathis, Yeap, Bu Beng, Stuckey, Bronwyn G A, Shankara-Narayana, Nandini, Conway, Ann J, Inder, Warrick, McLachlan, Robert I, Allan, Carolyn A, Jenkins, Alicia, Jesudason, David R, Bracken, Karen, Robledo, Kristy, Wittert, Gary A
Publicado 2023

Loss of the Nuclear Receptor Corepressor SLIRP Compromises Male Fertility

por Colley, Shane M., Wintle, Larissa, Searles, Richelle, Russell, Victoria, Firman, Renee C., Smith, Stephanie, DeBoer, Kathleen, Merriner, D. Jo, Genevieve, Ben, Bentel, Jacqueline M., Stuckey, Bronwyn G. A., Phillips, Michael R., Simmons, Leigh W., de Kretser, David M., O'Bryan, Moira K., Leedman, Peter J.
Publicado 2013

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

por Day, Felix, Karaderi, Tugce, Jones, Michelle R., Meun, Cindy, He, Chunyan, Drong, Alex, Kraft, Peter, Lin, Nan, Huang, Hongyan, Broer, Linda, Magi, Reedik, Saxena, Richa, Laisk, Triin, Urbanek, Margrit, Hayes, M. Geoffrey, Thorleifsson, Gudmar, Fernandez-Tajes, Juan, Mahajan, Anubha, Mullin, Benjamin H., Stuckey, Bronwyn G. A., Spector, Timothy D., Wilson, Scott G., Goodarzi, Mark O., Davis, Lea, Obermayer-Pietsch, Barbara, Uitterlinden, André G., Anttila, Verneri, Neale, Benjamin M., Jarvelin, Marjo-Riitta, Fauser, Bart, Kowalska, Irina, Visser, Jenny A., Andersen, Marianne, Ong, Ken, Stener-Victorin, Elisabet, Ehrmann, David, Legro, Richard S., Salumets, Andres, McCarthy, Mark I., Morin-Papunen, Laure, Thorsteinsdottir, Unnur, Stefansson, Kari, Styrkarsdottir, Unnur, Perry, John R. B., Dunaif, Andrea, Laven, Joop, Franks, Steve, Lindgren, Cecilia M., Welt, Corrine K.
Publicado 2018

Correction: Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

por Day, Felix, Karaderi, Tugce, Jones, Michelle R., Meun, Cindy, He, Chunyan, Drong, Alex, Kraft, Peter, Lin, Nan, Huang, Hongyan, Broer, Linda, Magi, Reedik, Saxena, Richa, Laisk, Triin, Urbanek, Margrit, Hayes, M. Geoffrey, Thorleifsson, Gudmar, Fernandez-Tajes, Juan, Mahajan, Anubha, Mullin, Benjamin H., Stuckey, Bronwyn G. A., Spector, Timothy D., Wilson, Scott G., Goodarzi, Mark O., Davis, Lea, Obermayer-Pietsch, Barbara, Uitterlinden, André G., Anttila, Verneri, Neale, Benjamin M., Jarvelin, Marjo-Riitta, Fauser, Bart, Kowalska, Irina, Visser, Jenny A., Andersen, Marianne, Ong, Ken, Stener-Victorin, Elisabet, Ehrmann, David, Legro, Richard S., Salumets, Andres, McCarthy, Mark I., Morin-Papunen, Laure, Thorsteinsdottir, Unnur, Stefansson, Kari, Styrkarsdottir, Unnur, Perry, John R. B., Dunaif, Andrea, Laven, Joop, Franks, Steve, Lindgren, Cecilia M., Welt, Corrine K.
Publicado 2019