Works by Quinton, Richard

Results: 109
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    Testosterone treatment is not associated with increased risk of adverse cardiovascular events: results from the Registry of Hypogonadism in Men (RHYME).

    Published in:
    2016
    By:
    • Maggi, Mario;
    • Wu, Frederick C.W.;
    • Jones, Thomas H.;
    • Jackson, Graham;
    • Behre, Hermann M.;
    • Hackett, Geoffrey;
    • Martin‐Morales, Antonio;
    • Balercia, Giancarlo;
    • Dobs, Adrian S.;
    • Arver, Stefan T.E.;
    • Maggio, Marcello;
    • Cunningham, Glenn R.;
    • Isidori, Andrea M.;
    • Quinton, Richard;
    • Wheaton, Olivia A.;
    • Siami, Flora S.;
    • Rosen, Raymond C.;
    • Meuleman, E.;
    • Dohle, G.;
    • Wu, F.
    Publication type:
    journal article
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    KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.

    Published in:
    EMBO Molecular Medicine, 2017, v. 9, n. 10, p. 1379, doi. 10.15252/emmm.201607376
    By:
    • Xu, Cheng;
    • Messina, Andrea;
    • Somm, Emmanuel;
    • Miraoui, Hichem;
    • Kinnunen, Tarja;
    • Acierno, James;
    • Niederländer, Nicolas J;
    • Bouilly, Justine;
    • Dwyer, Andrew A;
    • Sidis, Yisrael;
    • Cassatella, Daniele;
    • Sykiotis, Gerasimos P;
    • Quinton, Richard;
    • De Geyter, Christian;
    • Dirlewanger, Mirjam;
    • Schwitzgebel, Valérie;
    • Cole, Trevor R;
    • Toogood, Andrew A;
    • Kirk, Jeremy MW;
    • Plummer, Lacey
    Publication type:
    Article
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    IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed puberty.

    Published in:
    EMBO Molecular Medicine, 2016, v. 8, n. 6, p. 626, doi. 10.15252/emmm.201606250
    By:
    • Howard, Sasha R;
    • Guasti, Leonardo;
    • Ruiz‐Babot, Gerard;
    • Mancini, Alessandra;
    • David, Alessia;
    • Storr, Helen L;
    • Metherell, Lousie A;
    • Sternberg, Michael JE;
    • Cabrera, Claudia P;
    • Warren, Helen R;
    • Barnes, Michael R;
    • Quinton, Richard;
    • Roux, Nicolas;
    • Young, Jacques;
    • Guiochon‐Mantel, Anne;
    • Wehkalampi, Karoliina;
    • André, Valentina;
    • Gothilf, Yoav;
    • Cariboni, Anna;
    • Dunkel, Leo
    Publication type:
    Article
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    DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.

    Published in:
    Human Molecular Genetics, 2018, v. 27, n. 2, p. 359, doi. 10.1093/hmg/ddx408
    By:
    • Bouilly, Justine;
    • Messina, Andrea;
    • Papadakis, Georgios;
    • Cassatella, Daniele;
    • Cheng Xu;
    • Acierno, James S.;
    • Tata, Brooke;
    • Sykiotis, Gerasimos;
    • Santini, Sara;
    • Sidis, Yisrael;
    • Elowe-Gruau, Eglantine;
    • Franziska Phan-Hug;
    • Hauschild, Michael;
    • Bouloux, Pierre-Marc;
    • Quinton, Richard;
    • Lang-Muritano, Mariarosaria;
    • Favre, Lucie;
    • Marino, Laura;
    • Giacobini, Paolo;
    • Dwyer, Andrew A.
    Publication type:
    Article
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    Induction of puberty.

    Published in:
    European Journal of Endocrinology, 2014, v. 170, n. 6, p. R229, doi. 10.1530/EJE-13-0894
    By:
    • Dunkel, Leo;
    • Quinton, Richard
    Publication type:
    Article
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    Vitamin D and COVID-19-Revisited.

    Published in:
    Journal of Internal Medicine, 2022, v. 292, n. 4, p. 604, doi. 10.1111/joim.13536
    By:
    • Subramanian, Sreedhar;
    • Griffin, George;
    • Hewison, Martin;
    • Hopkin, Julian;
    • Kenny, Rose Anne;
    • Laird, Eamon;
    • Quinton, Richard;
    • Thickett, David;
    • Rhodes, Jonathan M.
    Publication type:
    Article
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    NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice.

    Published in:
    Science Translational Medicine, 2022, v. 14, n. 665, p. 1, doi. 10.1126/scitranslmed.abh2369
    By:
    • Chachlaki, Konstantina;
    • Messina, Andrea;
    • Delli, Virginia;
    • Leysen, Valerie;
    • Maurnyi, Csilla;
    • Huber, Chieko;
    • Ternier, Gaëtan;
    • Skrapits, Katalin;
    • Papadakis, Georgios;
    • Shruti, Sonal;
    • Kapanidou, Maria;
    • Cheng, Xu;
    • Acierno, James;
    • Rademaker, Jesse;
    • Rasika, Sowmyalakshmi;
    • Quinton, Richard;
    • Niedziela, Marek;
    • L'Allemand, Dagmar;
    • Pignatelli, Duarte;
    • Dirlewander, Mirjam
    Publication type:
    Article
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    In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism.

    Published in:
    European Journal of Endocrinology, 2017, v. 177, n. 3, p. 257, doi. 10.1530/EJE-17-0293
    By:
    • Salvatori, Roberto;
    • Radian, Serban;
    • Diekmann, Yoan;
    • Iacovazzo, Donato;
    • David, Alessia;
    • Gabrovska, Plamena;
    • Grassi, Giorgia;
    • Bussell, Anna-Marie;
    • Stals, Karen;
    • Weber, Astrid;
    • Quinton, Richard;
    • Crowne, Elizabeth C.;
    • Corazzini, Valentina;
    • Metherell, Lou;
    • Kearney, Tara;
    • Du Plessis, Daniel;
    • Sinha, Ajay Kumar;
    • Baborie, Atik;
    • Lecoq, Anne-Lise;
    • Chanson, Philippe
    Publication type:
    Article
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    Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein ( AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations.

    Published in:
    Clinical Endocrinology, 2009, v. 70, n. 2, p. 259, doi. 10.1111/j.1365-2265.2008.03379.x
    By:
    • Igreja, Susana;
    • Chahal, Harvinder S.;
    • Akker, Scott A.;
    • Gueorguiev, Maria;
    • Popovic, Vera;
    • Damjanovic, Svetozar;
    • Burman, Pia;
    • Wass, John A.;
    • Quinton, Richard;
    • Grossman, Ashley B.;
    • Korbonits, Márta
    Publication type:
    Article
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    Kallmann's syndrome: is it always for life?

    Published in:
    Clinical Endocrinology, 1999, v. 50, n. 4, p. 481, doi. 10.1046/j.1365-2265.1999.00708.x
    By:
    • Quinton;
    • Cheow;
    • Tymms;
    • Bouloux;
    • Wu;
    • Jacobs;
    • Quinton, Richard
    Publication type:
    Article
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    Kisspeptin-54 Accurately Identifies Hypothalamic Gonadotropin-Releasing Hormone Neuronal Dysfunction in Men with Congenital Hypogonadotropic Hypogonadism.

    Published in:
    Neuroendocrinology, 2021, v. 111, n. 12, p. 1176, doi. 10.1159/000513248
    By:
    • Abbara, Ali;
    • Eng, Pei Chia;
    • Phylactou, Maria;
    • Clarke, Sophie A.;
    • Mills, Edouard;
    • Chia, Germaine;
    • Yang, Lisa;
    • Izzi-Engbeaya, Chioma;
    • Smith, Neil;
    • Jayasena, Channa N.;
    • Comninos, Alexander N.;
    • Anand-Ivell, Ravinder;
    • Rademaker, Jesse;
    • Xu, Cheng;
    • Quinton, Richard;
    • Pitteloud, Nelly;
    • Dhillo, Waljit S.
    Publication type:
    Article
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    The effects and safety of testosterone replacement therapy for men with hypogonadism: the TestES evidence synthesis and economic evaluation.

    Published in:
    Health Technology Assessment, 2024, v. 28, n. 40-50, p. v
    By:
    • Cruickshank, Moira;
    • Hudson, Jemma;
    • Hernández, Rodolfo;
    • Aceves-Martins, Magaly;
    • Quinton, Richard;
    • Gillies, Katie;
    • Aucott, Lorna S.;
    • Kennedy, Charlotte;
    • Manson, Paul;
    • Oliver, Nicholas;
    • Wu, Frederick;
    • Bhattacharya, Siladitya;
    • Dhillo, Waljit S.;
    • Jayasena, Channa N.;
    • Brazzelli, Miriam
    Publication type:
    Article