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Titolo Data di pubblicazione Autore(i) File
Clinical and cytogenetic study of a case of trisomy 1q with familial translocation t(1;5)(q42;p15.3) 1-gen-1979 M. T., Duillo; DE TONI, Teresina; G., Cavaliere; G. L., Bava; A., Arslanian; Bonioli, Eugenio; Vianello, MARIA GRAZIA
Due casi di difficile inquadramento: coreoatetosi e sordità in fratelli 1-gen-1988 DE TONI, Teresina; Bruschettini, PIER LUIGI
Adolescenza. Verso un approccio multidisciplinare 1-gen-1992 E., de Toni; DE TONI, Teresina; R., Gastaldi; Palumbo, Mauro
Further case of metaphyseal acroscyphodysplasia with cone-shaped epiphyses (Bellini disease or metaphyseal dyschondroplasia). 1-gen-2008 DE TONI, Teresina; Baban, A; Colombo, E; Arnello, A; Divizia, Mt; Lerone, M.
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 1-gen-2008 Baban, A; Moresco, L; Divizia, Mt; Rossi, A; Ravazzolo, Roberto; Lerone, M; DE TONI, Teresina
The Italian National Survey for Prader-Willi syndrome: an epidemiologic study. 1-gen-2008 Grugni, G; Crinò, A; Bosio, L; Corrias, A; Cuttini, M; DE TONI, Teresina; DI BATTISTA, ELIANA MARIA; Franzese, A; Gargantini, L; Greggio, N; Iughetti, L; Livieri, C; Naselli, Arturo; Pagano, C; Pozzan, G; Ragusa, L; Salvatoni, A; Trifirò, G; Beccaria, L; Bellizzi, M; Bellone, J; Brunani, A; Cappa, M; Caselli, G; Cerioni, V; Delvecchio, M; Giardino, D; Iannì, F; Memo, L; Pilotta, A; Pomara, C; Radetti, G; Sacco, M; Sanzari, A; Sartorio, A; Tonini, G; Vettor, R; Zaglia, F; Chiumello, G.
Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study. 1-gen-2008 D'Annunzio, G; Minuto, N; D'Amato, E; DE TONI, Teresina; Lombardo, F; Pasquali, L; Lorini, RENATA GIUSEPPINA
Clinical and genetic characterization of Chanarin-Dorfman syndrome 1-gen-2008 Bruno, C; Bertini, E; DI ROCCO, M; Cassandrini, D; Ruffa, G; DE TONI, Teresina; Seri, M; Spada, M; LI VOLTI, G; D'Amico, A; Trucco, F; Arca, M; Casali, C; Angelini, C; Dimauro, S; Minetti, Carlo
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs. 1-gen-2009 3: Crinò, A; Di Giorgio, G; Livieri, C; Grugni, G; Beccaria, L; Bosio, L; Corrias, A; Chiumello, G; Trifirò, G; Salvatoni, A; Tonini, G; Gargantini, L; DE TONI, Teresina; Valerio, G; Ragusa, L; Franzese, A; Rinaldi, Mm; Spera, S; Gattinara, Gc; Villani, S; Iughetti, L; Genetic Obesity Study, Group; Italian Society of Pediatric, Endocrinology; Diabetology,
A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia. 1-gen-2011 van Kogelenberg, M; Lerone, M; DE TONI, Teresina; Divizia, Mt; de Brouwer, Ap; Veltman, Ja; van Bokhoven, H; Department of Paediatrics, Robertson S. P.; Child, Health; Dunedin School of, Medicine; Otago, University; Dunedin, ; New, Zealand
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome. 1-gen-2011 Grugni, G; Crinò, A; Pagani, S; Meazza, C; Buzi, F; DE TONI, Teresina; Gargantini, L; Pilotta, A; Pozzan, Gb; Radetti, G; Ragusa, L; Salvatoni, A; Sartorio, A; Bozzola, M; Genetic Obesity Study Group Italian Society of Pediatric, Endocrinology; Diabetology,
Growth hormone secretory pattern in non-obese children and adolescents with Prader-Willi syndrome 1-gen-2011 Grugni, G; Crinò, A; Pagani, S; Meazza, C; Buzi, F; DE TONI, Teresina; Gargantini, L; Pilotta, A; Pozzan, Gb; Radetti, G; Ragusa, L; Salvatoni, A; Sartorio, A; Bozzola, M; Genetic Obesity Study Group Italian Society of Pediatric, Endocrinology; Diabetology,
Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients. 1-gen-2013 Santen, Gw; Aten, E; Vulto van Silfhout, At; Pottinger, C; van Bon, Bw; van Minderhout, Ij; Snowdowne, R; van der Lans, Ca; Boogaard, M; Linssen, Mm; Vijfhuizen, L; van der Wielen, Mj; Vollebregt, Mj; Breuning, Mh; Kriek, M; van Haeringen, A; den Dunnen, Jt; Hoischen, A; Clayton Smith, J; de Vries, Bb; Hennekam, Rc; van Belzen, Mj; Coffin Siris, Consortium; DE TONI, Teresina
Mostrati risultati da 1 a 13 di 13
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