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1دورية أكاديمية
المؤلفون: Heard, JM, Vrinten, C, Schlander, M, Bellettato, CM, van Lingen, C, Scarpa, M, Matthijs, G, Nassogne, MC, Debray, FG, Roland, D, Chamova, T, Kozich, V, Pavel, J, Zenker, M, Lampe, C, Das, AM, Hennermann, J, Kolker, S, Weinhold, N, Mohnike, K, Gruenert, S, Lund, AM, Morales-Conejo, M, del Toro-Riera, M, Aldamiz-Echevarria, L, Garcia-Silva, MT, Schiff, M, Gouya, L, Labrune, P, de Lonlay, P, Belmatoug, N, Germain, DP, Cano, A, Dobbelaere, D, Jones, S, Dawson, C, Deegan, P, Santra, S, Vijay, S, Ramadza, DP, Baric, I, Zigman, T, Pflieger, G, Szakszon, K, Kaposta, R, Gasperini, S, Burlina, A, Parenti, G, Strisciuglio, P, Ceccarini, G, Federico, A, Simonati, A, Tumiene, B, Huidekoper, H, van Spronsen, F, Bosch, A, Rubio-Gozalbo, ME, Visser, G, Tangeraas, T, Aarsand, A, Kiec-Wilk, B, Gaspar, AMSM, Quelhas, D, Leao-Teles, E, Azevedo, O, Silva, EMFR, Matos, LMDFD, Martins, E, Lajic, S, Darin, N, Groselj, U, Tansek, MZ
المصدر: Orphanet journal of rare diseases. 15(1):3
مصطلحات موضوعية: Medicin och hälsovetenskap
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2دورية أكاديمية
المؤلفون: Heard, JM, Bellettato, C, Lingen, C, Scarpa, M, Debray, FG, Nassogne, MC, van Coster, R, De Meirleir, L, Eyskens, F, Morava, E, Baric, I, Kozich, V, Lund, AM, Germain, D, Belmatoug, N, Guffon, N, Labrune, P, Gouya, L, De Lonlay, P, Schiff, M, Dobbelaere, D, Chabrol, B, Ploeckinger, U, Das, AM, Spiekerkoetter, U, Rutsch, F, Mohnike, K, Hahn, A, Kolker, S, Ullrich, K, Hennermann, J, Balogh, I, Bembi, B, Donati, MA, Gasperini, S, Parenti, G, Salviati, A, Vici, CD, Di Rocco, M, Cefalo, G, Burlina, A, Ceccarini, G, Federico, A, Van der Ploeg, A, Rubio-Gozalbo, ME, Van Spronsen, F, Visser, G, Bosch, A, Tangeraas, T, Sanderberg, S, Kiec-Wilk, B, Gaspar, AMSM, Martins, E, Silva, EMFR, Matos, LMDFD, Azevedo, O, Tansek, MZ, Couce-Pico, ML, Cazorla, AG, Azuara, LAE, Del Toro-Riera, M, Silva, MTG, Lajic, S, Darin, N, Deegan, P, Vijay, S, Chronopolou, E, Jones, S, Chakrapani, A, Hiwot, T
المصدر: Orphanet journal of rare diseases. 14(1):119
مصطلحات موضوعية: Medicin och hälsovetenskap
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3
المؤلفون: Heard, J. M., Vrinten, C., Schlander, M., Bellettato, C. M., van Lingen, C., Scarpa, M., Matthijs, G., Nassogne, M. C., Debray, F. G., Roland, D., Chamova, T., Kozich, V., Pavel, J., Zenker, M., Lampe, C., Das, A. M., Hennermann, J., Kolker, S., Weinhold, N., Mohnike, K., Gruenert, S., Lund, A. M., Morales-Conejo, M., del Toro-Riera, M., Aldamiz-Echevarria, L., Garcia-Silva, M. T., Schiff, M., Gouya, L., Labrune, P., de Lonlay, P., Belmatoug, N., Germain, D. P., Cano, A., Dobbelaere, D., Jones, S., Dawson, C., Deegan, P., Santra, S., Vijay, S., Ramadza, D. P., Baric, I., Aigman, T., Pflieger, G., Szakszon, K., Kaposta, R., Gasperini, S., Burlina, A., Parenti, G., Strisciuglio, P., Ceccarini, G., Federico, A., Simonati, A., Tumiene, B., Huidekoper, H., van Spronsen, F., Bosch, A., Rubio-Gozalbo, M. E., Visser, G., Tangeraas, T., Aarsand, A., Kiec-Wilk, B., Gaspar, Amsm, Quelhas, D., Leao-Teles, E., Azevedo, O., Silva, Emfr, Matos, Lmdfd, Martins, E., Lajic, S., Darin, Niklas, 1964, Groselj, U., Tansek, M. Z.
المصدر: Orphanet Journal of Rare Diseases. 15(1)
مصطلحات موضوعية: Clinical Medicine, Klinisk medicin, Orphan medicinal product, Access to treatment, European Reference, Network, Hereditary Metabolic Diseases, Inborn errors of metabolism, drugs, Genetics & Heredity, Research & Experimental Medicine
URL الوصول: https://gup.ub.gu.se/publication/290941