Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fertz, M. C."'
Publikováno v:
Case Reports in Pediatrics.
Prader-Willi syndrome in the newborn is essentially characterized by marked hypotonia, feeding difficulties, hypogonadism, and possible characteristic facial features. However, diagnosis at this age may be particularly difficult, and dysmorphic featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=hindawi_publ::bad8dfe68f9203efbc56fc366d43b765
Autor:
de Vonderweid, U, Spagnolo, A, Corchia, C, Chiandotto, V, Chiappe, S, Chiappe, F, Colarizi, P, De Luca, T, Didato, M, Fertz, M C
Publikováno v:
Acta Paediatrica; Apr1994, Vol. 83 Issue 4, p391-396, 6p
Publikováno v:
Clinical Genetics; Apr1990, Vol. 37 Issue 4, p271-278, 8p
Autor:
Console, V., Gagliardi, L., Giorgi, A., Ponti, E., Di Stefano, G., Romeo, M. G., Senderi, A., Dipietro, M., Pisano, F., Silvano, S., Anghileri, M., Zanini, R., Lanza, E., Pellizzari, N., Raimondi, A. M., Brambilla, M. L., Marsili, M. T., Rosti, D., Bettinelli, M. E., Accerta, S., Spinelli, D., Borroni, C., Abbiari, L., Carlevaro, C., Bertazzi, E., Zaramella, P., Perrone, S., Didato, M. A., Gioeli, A., Cascio, G., Scimeni, M., Volante, E., Gambini, L., Neri, F., Maserati, A., Chinco, G., Migliori, C., Bianchi, P. E., Rosanna Guagliano, Romagnoli, C., Gallini, F., Mintcucci, G., Ricci, R., Guala, G., Fogli, L., Anselmetti, G., Berti, M. R., Pedrotti, D., Zampedri, E., Silva, S., Fertz, M. C., Perissutti, P.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::204b084dc99be726d752a40fb60c49d0
http://www.scopus.com/inward/record.url?eid=2-s2.0-7344243177&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-7344243177&partnerID=MN8TOARS
Publikováno v:
Minerva pediatrica [Minerva Pediatr] 1990 Mar; Vol. 42 (3), pp. 67-72.