Brain imaging and genetics in patients with congenital hypogonadotropic hypogonadism: a multicenter Belgian study.

التفاصيل البيبلوغرافية
العنوان: Brain imaging and genetics in patients with congenital hypogonadotropic hypogonadism: a multicenter Belgian study.
Imagerie cérébrale et génétique chez les patients avec un hypogonadisme hypogonadotrope congénital: une étude multicentrique belge
المؤلفون: VALDES SOCIN, Hernan Gonzalo, LIBIOULLE, Cécile, HARVENGT, Julie, Pintiaux, Axelle, JONAS, Corinne, PARENT, Anne-Simone, GEENEN, Vincent, CORMAN, Vinciane, Debray, François-Guillaume, DIDEBERG, Vinciane, T'Sjoen, Guy, De Leerner, A, Beckers, D, Destree, A, Roland, D, Lederer, D, Boscolo, M, BOURS, Vincent, Maiter, Dominique, BECKERS, Albert
المساهمون: Service d'Endocrinologie
المصدر: NENEG Abstract Book Communications, 64 (2018-04-19); Northern-European Neuro-Endocrine Group, Aarhus, Denmark [DK], 18-20 avril 2018
بيانات النشر: Pfizer, 2018.
سنة النشر: 2018
مصطلحات موضوعية: kallmann, mutation, hypogonadotropic hypogonadism, brain MRI, anosmia, FGFR1, KISSR, TAC3, TACR3, CHD7, next generation sequencing, Chiari type 1 malformation, Human health sciences, Endocrinology, metabolism & nutrition, Sciences de la santé humaine, Endocrinologie, métabolisme & nutrition
الوصف: Etude rétrospective et prospective du génotype et du phénotype chez les patients atteints d’un hypogonadisme hypogonadotrope congénital
نوع الوثيقة: conference paper
http://purl.org/coar/resource_type/c_5794Test
conferenceObject
peer reviewed
اللغة: English
الوصول الحر: https://orbi.uliege.be/handle/2268/223610Test
حقوق: open access
http://purl.org/coar/access_right/c_abf2Test
info:eu-repo/semantics/openAccess
رقم الانضمام: edsorb.223610
قاعدة البيانات: ORBi