Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Street, M. E."'
Akademický článek
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Autor:
Cannavo, S., Cappa, M., Ferone, D., Isidori, A. M., Loche, S., Salerno, M., Maghnie, M., Aimaretti, G., Ambrosio, M. R., Bellone, S., Caruso, M., Castello, R., Ceccato, F., Cerbone, T., Cherubini, V., de Carlo, E., De Sanctis, L., della Casa, S., Di Somma, C., Faienza, M. F., Gasco, V., Gaudino, R., Giacomozzi, C., Giavoli, C., Guazzarotti, L., Klain, A., Lania, A., Leonardi, D., Longhi, S., Lughetti, L., Maggio, M. C., Wasniewska, G. M., Mameli, C., Mauro, C., Giudice, E. M. D., Palermo, M. C. A., Parpagnoli, M., Persani, L., Pilotta, A., Pozzobon, G., Rochira, V., Rota, F., Sacco, M., Scarcella, S., Scavuzzo, F., Sinisi, A. A., Street, M. E., Tornese, G.
Growth hormone deficiency (GHD) describes the impairment of growth hormone (GH) secretion by the pituitary somatotroph cells. GHD may be congenital, with causes, including genetic alterations and structural brain malformations, or acquired, including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c29cf3ca5f60ad235911653d55e79b72
https://hdl.handle.net/11368/3029426
https://hdl.handle.net/11368/3029426
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mansueto, M. L., Zagni, G., Sartori, C., Bermudez, B. A. O., Righi, B., Catellani, C., Fusco, C., Frasoldati, A., De Fanti, A., Iughetti, L., Street, M. E.
Publikováno v:
Acta bio-medica : Atenei Parmensis. 92(S1)
Hashimoto's thyroiditis (HT) is a common endocrinopathy in children, particularly in females. Clinical overt presentation of hypothyroidism in HT includes mild to very severe forms, characterised by impairment of many body functions and organs, such
Autor:
Maltoni, G., Zioutas, M., Iughetti, L., Predieri, B., Iovane, B., Lazzeroni, P., Street, M. E., Lasagni, A., Graziani, V., Suprani, T., De Luca, F., Riboni, S., Sogno Valin, P., Mainetti, B., Libertucci, F., Zucchini, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3674::044c64a9a7ac615b3ff1274abb66c084
https://hdl.handle.net/11380/1255137
https://hdl.handle.net/11380/1255137
Autor:
Ivanovski I., Djuric O., Broccoli S., Caraffi S. G., Accorsi P., Adam M. P., Avela K., Badura-Stronka M., Bayat A., Clayton-Smith J., Cocco I., Cordelli D. M., Cuturilo G., Di Pisa V., Dupont Garcia J., Gastaldi R., Giordano L., Guala A., Hoei-Hansen C., Inaba M., Iodice A., Nielsen J. E. K., Kuburovic V., Lazalde-Medina B., Malbora B., Mizuno S., Moldovan O., Moller R. S., Muschke P., Otelli V., Pantaleoni C., Piscopo C., Poch-Olive M. L., Prpic I., Marin Reina P., Raviglione F., Ricci E., Scarano E., Simonte G., Smigiel R., Tanteles G., Tarani L., Trimouille A., Valera E. T., Schrier Vergano S., Writzl K., Callewaert B., Savasta S., Street M. E., Iughetti L., Bernasconi S., Giorgi Rossi P., Garavelli L.
Publikováno v:
Ivanovski, I, Djuric, O, Broccoli, S, Caraffi, S G, Accorsi, P, Adam, M P, Avela, K, Badura-Stronka, M, Bayat, A, Clayton-Smith, J, Cocco, I, Cordelli, D M, Cuturilo, G, Di Pisa, V, Dupont Garcia, J, Gastaldi, R, Giordano, L, Guala, A, Hoei-Hansen, C, Inaba, M, Iodice, A, Nielsen, J E K, Kuburovic, V, Lazalde-Medina, B, Malbora, B, Mizuno, S, Moldovan, O, Møller, R S, Muschke, P, Otelli, V, Pantaleoni, C, Piscopo, C, Poch-Olive, M L, Prpic, I, Marín Reina, P, Raviglione, F, Ricci, E, Scarano, E, Simonte, G, Smigiel, R, Tanteles, G, Tarani, L, Trimouille, A, Valera, E T, Schrier Vergano, S, Writzl, K, Callewaert, B, Savasta, S, Street, M E, Iughetti, L, Bernasconi, S, Giorgi Rossi, P & Garavelli, L 2020, ' Mowat-Wilson syndrome : growth charts ', Orphanet Journal of Rare Diseases, vol. 15, 151 . https://doi.org/10.1186/s13023-020-01418-4
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Orphanet Journal of Rare Diseases
ORPHANET JOURNAL OF RARE DISEASES
Volume 15
Issue 1
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Orphanet Journal of Rare Diseases
ORPHANET JOURNAL OF RARE DISEASES
Volume 15
Issue 1
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Background: Mowat–Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or deletions of the ZEB2 gene. It is characterized by moderate-severe intellectual disability, epilepsy, Hirschsprung disease and multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36eb6ffaf0310403b7e7418f5c8baafa
https://curis.ku.dk/portal/da/publications/mowatwilson-syndrome(958dfaa0-b4f4-4afb-bc1b-f587e943a8f5).html
https://curis.ku.dk/portal/da/publications/mowatwilson-syndrome(958dfaa0-b4f4-4afb-bc1b-f587e943a8f5).html
Autor:
Street, M. E., Smerieri, A., Montanini, L., Predieri, B., Iughetti, L., Valenzise, M., Luca, F., Vigone, M., Giovanna WEBER, Maghnie, M., Bernasconi, S.
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Barbara PREDIERI
Scopus-Elsevier
Barbara PREDIERI
Obesity is a state of chronic inflammation. Data on IGF system are often discrepant, and their relationships with mediators of inflammation are unknown. Furthermore, changes in thyroid function have been reported. We aimed at investigating the change
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0c0b6733d099503a7ba6684afb6a1327
http://hdl.handle.net/11570/2555087
http://hdl.handle.net/11570/2555087
Autor:
Iughetti, Lorenzo, Vannelli, S., Pirazzoli, P., Bertelloni, S., Radetti, G., Street, M. E., Madeo, S., Mazzanti, L., Ghione, S., Stasiowska, B., Predieri, Barbara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3674::0350966f9b1c2404ec3913c33dd7fa15
https://hdl.handle.net/11380/740103
https://hdl.handle.net/11380/740103
Autor:
Federico, G., Street, M. E., Maghnie, M., Caruso-Nicoletti, M., Loche, S., Bertelloni, S., Cianfarani, S., Aimaretti, G., Antoniazzi, F., Arrigo, T., Bellone, J., Bellone, S., Bozzola, M., Buzi, F., Cappa, M., Cisternino, M., De Luca, F., Del Vecchio, M., Galluzzi, F., Germani, D., Ghirri, P., Ghizzoni, L., Greggio, N. A., Iughetti, L., Losi, S., Luciano, A., Maffeis, C., Modestini, E., Pirazzoli, P., Pozzobon, G., Predieri, B., Rusconi, R., Salerno, M. C., Salvatoni, A., Sciré, G., Scommegna, S., Spadoni, G. L., Sposito, M., Wasniewska, M., Zampolli, M., Zucchini, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3660::a8eb015d309acd04f463fe4ab25bd340
http://hdl.handle.net/11383/2068329
http://hdl.handle.net/11383/2068329