Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic SLC30A9 Pathogenic Variants von Steel, DBD, Danti, FR, Abunada, M, Kamien, B, Malhotra, S, Topf, M, Kaliakatsos, M, Valentine, J, Nemeth, AH, Jayawant, S, Reid, KM, Mankad, K, Sudhakar, S, Ben-Pazi, H, Barwick, K, Kurian, MA

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The expanding spectrum of movement disorders in genetic epilepsies von Papandreou, A, Danti, FR, Spaull, R, Leuzzi, V, Mctague, A, Kurian, MA

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GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome von Danti, FR, Galosi, S, Romani, M, Montomoli, M, Carss, KJ, Raymond, FL, Parrini, E, Bianchini, C, McShane, T, Dale, RC, Mohammad, SS, Shah, U, Mahant, N, Ng, J, McTague, A, Samanta, R, Vadlamani, G, Valente, EM, Leuzzi, V, Kurian, MA, Guerrini, R

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, GI, Kitabayashi, N, Barth, M, Briggs, TA, Burton, ACE, Carpanelli, ML, Cerisola, AM, Colson, C, Dale, RC, Danti, FR, Darin, N, De Azua, B, De Giorgis, V, De Goede, CGL, Desguerre, I, De laet, C, Eslahi, A, Fahey, MC, Fallon, P, Fay, A, Fazzi, E, Gorman, MP, Gowrinathan, NR, Hully, M, Kurian, MA, Leboucq, N, Lin, J-PS-M, Lines, MA, Mar, SS, Maroofian, R, Marti-Sanchez, L, McCullagh, G, Mojarrad, M, Narayanan, V, Orcesi, S, Ortigoza-Escobar, JD, Perez-Duenas, B, Petit, F, Ramsey, KM, Rasmussen, M, Rivier, F, Rodriguez-Pombo, P, Roubertie, A, Stodberg, TI, Toosi, MB, Toutain, A, Uettwiller, F, Ulrick, N, Vanderver, A, Waldman, A, Livingston, JH, Crow, YJ

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Lettres de Mr. l'abbé de Saint-L de Soissons, à Mr. le Baron de H (Heiss) sur différentes éditions rares du XVe siècle von Bartholomeus Mercier

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