Works matching IS 08044643 AND DT 2016 AND VI 175 AND IP 6

Results: 21
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    Germline mutations and genotype–phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.

    Published in:
    European Journal of Endocrinology, 2016, v. 175, n. 6, p. X3, doi. 10.1530/EJE-16-0126e
    By:
    • Pandit, Reshma;
    • Khadilkar, Kranti;
    • Sarathi, Vijaya;
    • Rajeev Kasaliwal, Rajeev Kasaliwal;
    • Goroshi, Manjunath;
    • Khare, Shruti;
    • Nair, Sandhya;
    • Raghavan, Vijaya;
    • Dalvi, Abhay;
    • Hira, Priya;
    • Fernandes, Gwendolyn;
    • Sathe, Pragati;
    • Rojekar, Amey;
    • Malhotra, Gaurav;
    • Bakshi, Ganesh;
    • Prakash, Gagan;
    • Bhansali, Anil;
    • Walia, Rama;
    • Kamalanathan, Sadishkumar;
    • Sahoo, Jayaprakash
    Publication type:
    Article
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    The androgen receptor gene CAG repeat in relation to 4-year changes in androgen-sensitive endpoints in community-dwelling older European men.

    Published in:
    European Journal of Endocrinology, 2016, v. 175, n. 6, p. 583, doi. 10.1530/EJE-16-0447
    By:
    • Eendebak, Robert J. A. H.;
    • Huhtaniemi, Ilpo T.;
    • Pye, Stephen R.;
    • Ahern, Tomas;
    • O'Neill, Terence W.;
    • Bartfai, György;
    • Casanueva, Felipe F.;
    • Maggi, Mario;
    • Forti, Gianni;
    • Alston, Robert D.;
    • Giwercman, Aleksander;
    • Han, Thang S.;
    • Kula, Krzysztof;
    • Lean, Michael E. J.;
    • Punab, Margus;
    • Pendleton, Neil;
    • Keevil, Brian G.;
    • Vanderschueren, Dirk;
    • Rutter, Martin K.;
    • Tampubolon, Gindo
    Publication type:
    Article
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    From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network.

    Published in:
    European Journal of Endocrinology, 2016, v. 175, n. 6, p. 1, doi. 10.1530/EJE-16-0107
    By:
    • Thiele, Susanne;
    • Mantovani, Giovanna;
    • Barlier, Anne;
    • Boldrin, Valentina;
    • Bordogna, Paolo;
    • Sanctis, Luisa De;
    • Elli, Francesca M.;
    • Freson, Kathleen;
    • Garin, Intza;
    • Grybek, Virginie;
    • Hanna, Patrick;
    • Izzi, Benedetta;
    • Hiort, Olaf;
    • Lecumberri, Beatriz;
    • Pereda, Arrate;
    • Saraff, Vrinda;
    • Silve, Caroline;
    • Turan, Serap;
    • Usardi, Alessia;
    • Werner, Ralf
    Publication type:
    Article
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    Single nucleotide polymorphisms in the intergenic region between metformin transporter OCT2 and OCT3 coding genes are associated with short-term response to metformin monotherapy in type 2 diabetes mellitus patients.

    Published in:
    European Journal of Endocrinology, 2016, v. 175, n. 6, p. 531, doi. 10.1530/EJE-16-0347
    By:
    • Zaharenko, Linda;
    • Kalnina, Ineta;
    • Geldnere, Kristine;
    • Konrade, Ilze;
    • Grinberga, Solveiga;
    • Židzik, Jozef;
    • Javorský, Martin;
    • Lejnieks, Aivars;
    • Nikitina-Zake, Liene;
    • Fridmanis, Davids;
    • Peculis, Raitis;
    • Radovica-Spalvina, Ilze;
    • Dace Hartmane;
    • Pugovics, Osvalds;
    • Tkáč, Ivan;
    • Klimčáková, Lucia;
    • Pīrāgs, Valdis;
    • Klovins, Janis
    Publication type:
    Article
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