Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ceccarini, G."'
Autor:
Caprio, M., Infante, M., Moriconi, E., Armani, A., Fabbri, A., Mantovani, G., Mariani, S., Lubrano, C., Poggiogalle, E., Migliaccio, S., Donini, L. M., Basciani, S., Cignarelli, A., Conte, E., Ceccarini, G., Bogazzi, F., Cimino, L., Condorelli, R. A., La Vignera, S., Calogero, A. E., Gambineri, A., Vignozzi, L., Prodam, F., Aimaretti, G., Linsalata, G., Buralli, S., Monzani, F., Aversa, A., Vettor, R., Santini, F., Vitti, P., Gnessi, L., Pagotto, U., Giorgino, F., Colao, A., Lenzi, A., Beccuti, G., Biondi, B., Cannavo, S., Chiodini, I., De Feudis, G., Di Francesco, S., Di Gregorio, A., Fallo, F., Foresta, C., Giacchetti, G., Granata, R., Isidori, A. M., Magni, P., Maiellaro, P., Caprino, M. P., Pivonello, R., Pofi, R., Pontecorvi, A., Simeoli, C.
Publikováno v:
Journal of Endocrinological Investigation. 42:1365-1386
Background: Weight loss is a milestone in the prevention of chronic diseases associated with high morbility and mortality in industrialized countries. Very-low calorie ketogenic diets (VLCKDs) are increasingly used in clinical practice for weight los
Autor:
Heard, J. -M., Bellettato, C, Van, Lingen, Scarpa, M, Debray, F. -G., Nassogne, M. -C., Van, Coster, Meirleir, De, Eyskens, L., Morava, F., Baric, E., Kozich, I., Lund, V., Germain, A. M., Belmatoug, D., Guffon, N., Labrune, N., Gouya, P., Lonlay, De, Schiff, P., Dobbelaere, M., Chabrol, D., Das, B., Spiekerkoetter, A. M., Rutsch, U., Ploeckinger, F., Mohnike, U., Hahn, K., Kölker, A., Ullrich, S., Balogh, K., Bembi, I., Donati, B., Gasperini, M. A., Parenti, S., Salviati, G., Vici, A., C. -D., Rocco, Di, Cefalo, M., Burlina, G., Ceccarini, G., Federico, A., Van Der Ploeg, Rubio-Gozalbo, A., M. -E., Van, Spronsen, Visser, F., Bosch, G., Tangeraas, A., Sanderberg, T., Kieć-Wilk, S., Gaspar, B., A. -M. S. M., Martins, E., Silva, E. -M. F. R., De Abreu Freire Diogo Matos, L. -M., Azevedo, O., Tansek, M. -Z., Couce-Pico, M. -L., Cazorla, A. G., Azuara, L. A. -E., Del, Toro-Riera, Lajic, M., Darin, S., Deegan, N., Vijaym, P., Chronopoulou, S., Jones, E., Chakrapani, S., Hiwot, A.
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Orphanet Journal of Rare Diseases, 14:119. BioMed Central Ltd.
Heard, J-M, Bellettato, C, van Lingen, C, Scarpa, M, Debray, F-G, Nassogne, M-C C, van Coster, R, de Meirleir, L, Eyskens, F, Morava, E, Baric, I, Kozich, V, Lund, A M, Germain, D, Belmatoug, N, Guffon, N, Labrune, P, Gouya, L, de Lonlay, P, Schiff, M, Dobbelaere, D, Chabrol, B, Das, A M, Spiekerkoetter, U, Rutsch, F, Ploeckinger, U, Mohnike, K, Hahn, A, Kölker, S, Ullrich, K, Balogh, I, Bembi, B, Donati, M A, Gasperini, S, Parenti, G, Salviati, A, Vici, C-D, di Rocco, M, Cefalo, G, Burlina, A, Ceccarini, G, Federico, A, van der Ploeg, A, Rubio-Gozalbo, M-E, van Spronsen, F, Visser, G, Bosch, A, Tangeraas, T, Sanderberg, S, Kieć-Wilk, B, Gaspar, A-M S M, Martins, E, Silva, E-M F R, de Abreu Freire Diogo Matos, L-M, Azevedo, O, Tansek, M-Z, Couce-Pico, M-L, Cazorla, A G, Azuara, L A-E, del Toro-Riera, M, Lajic, S, Darin, N, Deegan, P, Vijaym, S, Chronopoulou, E, Jones, S, Chakrapani, A & Hiwot, T 2019, ' Research activity and capability in the European reference network MetabERN ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, 119 . https://doi.org/10.1186/s13023-019-1091-8
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases
Orphanet Journal of Rare Diseases, 14:119. BioMed Central Ltd
ORPHANET JOURNAL OF RARE DISEASES
Orphanet Journal of Rare Diseases, 14(1):119. BioMed Central
Orphanet Journal of Rare Diseases, 14(1). BioMed Central
Orphanet journal of rare diseases, 14(1):119. BioMed Central
Orphanet Journal of Rare Diseases, 14:119. BioMed Central Ltd.
Heard, J-M, Bellettato, C, van Lingen, C, Scarpa, M, Debray, F-G, Nassogne, M-C C, van Coster, R, de Meirleir, L, Eyskens, F, Morava, E, Baric, I, Kozich, V, Lund, A M, Germain, D, Belmatoug, N, Guffon, N, Labrune, P, Gouya, L, de Lonlay, P, Schiff, M, Dobbelaere, D, Chabrol, B, Das, A M, Spiekerkoetter, U, Rutsch, F, Ploeckinger, U, Mohnike, K, Hahn, A, Kölker, S, Ullrich, K, Balogh, I, Bembi, B, Donati, M A, Gasperini, S, Parenti, G, Salviati, A, Vici, C-D, di Rocco, M, Cefalo, G, Burlina, A, Ceccarini, G, Federico, A, van der Ploeg, A, Rubio-Gozalbo, M-E, van Spronsen, F, Visser, G, Bosch, A, Tangeraas, T, Sanderberg, S, Kieć-Wilk, B, Gaspar, A-M S M, Martins, E, Silva, E-M F R, de Abreu Freire Diogo Matos, L-M, Azevedo, O, Tansek, M-Z, Couce-Pico, M-L, Cazorla, A G, Azuara, L A-E, del Toro-Riera, M, Lajic, S, Darin, N, Deegan, P, Vijaym, S, Chronopoulou, E, Jones, S, Chakrapani, A & Hiwot, T 2019, ' Research activity and capability in the European reference network MetabERN ', Orphanet Journal of Rare Diseases, vol. 14, no. 1, 119 . https://doi.org/10.1186/s13023-019-1091-8
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases
Orphanet Journal of Rare Diseases, 14:119. BioMed Central Ltd
ORPHANET JOURNAL OF RARE DISEASES
Orphanet Journal of Rare Diseases, 14(1):119. BioMed Central
Orphanet Journal of Rare Diseases, 14(1). BioMed Central
Orphanet journal of rare diseases, 14(1):119. BioMed Central
Background MetabERN is one of the 24 European Reference Networks created according to the European Union directive 2011/24/EU on patient’s rights in cross border healthcare. MetabERN associates 69 centres in 18 countries, which provide care for pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcb9bb5f88cf1f4a2664a07cea357d1d
https://doi.org/10.1186/s13023-019-1091-8
https://doi.org/10.1186/s13023-019-1091-8
Autor:
David B. Savage, Alessandra Gambineri, Raoul C.M. Hennekam, Claire Adams, Paolo Sbraccia, Jannik Schaaf, Julia von Schnurbein, David Araújo-Vilar, Camille Vatier, Giovanna Lattanzi, Konstanze Miehle, Baris Akinci, Giuseppe Novelli, Giovanni Ceccarini, Isabelle Jéru, Maria Rosaria D'Apice, Ferruccio Santini, Gabriele Nagel, Elena Vorona, Ekaterina Sorkina, George A. Tanteles, Martin Wabitsch, Corinne Vigouroux, Marie-Christine Vantyghem, Ermelinda Santos Silva
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases, 15(1):17. BioMed Central
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases, 15(1):17. BioMed Central
ClinicalTrials.gov (NCT03553420). Registered 14 March 2018, retrospectively registered Background: Lipodystrophy syndromes comprise a group of extremely rare and heterogeneous diseases characterized by a selective loss of adipose tissue in the absenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32435274f90dba49e2d2bf532e60fbd6
http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/52994
http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/52994