학술논문

Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA)
Document Type
Article
Author
Sauter, M.Belousova, E.Benedik, M.P.Carter, T.Cottin, V.Curatolo, P.Dahlin, M.D’Amato, L.Marques, R.d’Augères, G.B.de Vries, P.J.Ferreira, J.C.Feucht, M.Fladrowski, C.Hertzberg, C.Jozwiak, S.Lawson, J.A.Macaya, A.Nabbout, R.O’Callaghan, F.Qin, J.Sander, V.Shah, S.Takahashi, Y.Touraine, R.Youroukos, S.Zonnenberg, B.Jansen, A.Kingswood, J.C.Shinohara, N.Horie, S.Kubota, M.Tohyama, J.Imai, K.Kaneda, M.Kaneko, H.Uchida, Y.Kirino, T.Endo, S.Inoue, Y.Uruno, K.Serdaroglu, A.Yapici, Z.Anlar, B.Altunbasak, S.Lvova, O.Belyaev, O.V.Agranovich, O.Levitina, E.V.Maksimova, Y.V.Karas, A.Jiang, Y.Zou, L.Xu, K.Zhang, Y.Luan, G.Zhang, Y.Wang, Y.Jin, M.Ye, D.Liao, W.Zhou, L.Liu, J.Liao, J.Yan, B.Deng, Y.Jiang, L.Liu, Z.Huang, S.Li, H.Kim, K.Chen, P.-L.Lee, H.-F.Tsai, J.-D.Chi, C.-S.Huang, C.-C.Riney, K.Yates, D.Kwan, P.Likasitwattanakul, S.Nabangchang, C.Chomtho, L.T.K.Katanyuwong, K.Sriudomkajorn, S.Wilmshurst, J.Segel, R.Gilboa, T.Tzadok, M.Valevski, A.F.Papathanasopoulos, P.Papavasiliou, A.S.Giannakodimos, S.Gatzonis, S.Pavlou, E.Tzoufi, M.Vergeer, A.M.H.Dhooghe, M.Verhelst, H.Roelens, F.Nassogne, M.C.Defresne, P.De Waele, L.Leroy, P.Demonceau, N.Legros, B.Van Bogaert, P.Ceulemans, B.Dom, L.Castelnau, P.De Saint Martin, A.Riquet, A.Milh, M.Cances, C.Pedespan, J.-M.Ville, D.Roubertie, A.Auvin, S.Berquin, P.Richelme, C.Allaire, C.Gueden, S.Tich, S.N.T.Godet, B.Rojas, M.L.R.F.Planas, J.C.Bermejo, A.M.Dura, P.S.Aparicio, S.R.Gonzalez, M.J.M.Pison, J.L.Barca, M.O.B.Laso, E.L.Luengo, O.A.Rodriguez, F.J.A.Dieguez, I.M.Salas, A.C.Carrera, I.M.Salcedo, E.M.Petri, M.E.Y.Candela, R.C.da Conceicao Carrilho, I.Vieira, J.P.da Silva Oliveira Monteiro, J.P.de Oliveira Ferreira Leao, M.J.S.Luis, C.S.M.R.Mendonca, C.P.Endziniene, M.Strautmanis, J.Talvik, I.Canevini, M.P.Gambardella, A.Pruna, D.Buono, S.Fontana, E.Bernardina, B.D.Burloiu, C.Cosma, I.S.B.Vintan, M.A.Popescu, L.Zitterbart, K.Payerova, J.Bratsky, L.Zilinska, Z.Gruber-Sedlmayr, U.Baumann, M.Haberlandt, E.Rostasy, K.Pataraia, E.Elmslie, F.Johnston, C.A.Crawford, P.Uldall, P.Uvebrant, P.Rask, O.Bjoernvold, M.Brodtkorb, E.Sloerdahl, A.Solhoff, R.Jaatun, M.S.G.Mandera, M.Radzikowska, E.J.Wysocki, M.Fischereder, M.Kurlemann, G.Wilken, B.Wiemer-Kruel, A.Budde, K.Marquard, K.Knuf, M.Hahn, A.Hartmann, H.Merkenschlager, A.Trollmann, R.
Source
In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, December 2021, 16(1))
Subject
Language
English
ISSN
17501172