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Material Type: Artigo
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Proposal for a protocol for the staging of incontinentia pigmenti in pediatric agePortaleone, D ; Taroni, F ; Micheli, S ; Moioli, M ; Pedrazzini, A ; Cognizzoli, P ; Carnelli, VMinerva pediatrica, 2007-06, Vol.59 (3), p.255-265ItalyTexto completo disponível |
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Material Type: Artigo
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Neurobiology of autism: Study of a sample of autistic childrenGermanò, E ; Gagliano, A ; Magazù, A ; Calarese, T ; Calabrò, M E ; Bonsignore, M ; Tortorella, G ; Calamoneri, FMinerva pediatrica, 2006-04, Vol.58 (2), p.109-120ItalyTexto completo disponível |
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Material Type: Ata de Congresso
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Klinefelter syndromeRogol, Alan DActa bio-medica : Atenei Parmensis, 2003, Vol.74 (1), p.50-52 [Periódico revisado por pares]ItalyTexto completo disponível |
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Material Type: Artigo
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The Smith-Magenis syndrome: a new case with infant spasmsRoccella, M ; Parisi, LMinerva pediatrica, 1999-03, Vol.51 (3), p.65-71ItalyTexto completo disponível |
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Material Type: Artigo
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Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocationFioretti, G ; Pagano, L ; Renda, S ; Festa, B ; Rinaldi, A ; Celona, A ; Casullo, C ; Stabile, M ; Cavaliere, M L ; Ventruto, VMinerva pediatrica, 1980-06, Vol.32 (12), p.807-814ItalyTexto completo disponível |
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Material Type: Artigo
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A report of 2 cases of Turner's syndrome with a ring X chromosomeMigliori, M V ; Bartolotta, E ; Maurizi, M ; Bonazzi, P ; Cardinale, G ; Manunza, VMinerva pediatrica, 1991-09, Vol.43 (9), p.605-609ItalyTexto completo disponível |
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Material Type: Artigo
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Rheumatoid-like syndrome as a symptom of agammaglobulinemiaAmato, G M ; Barcellona, R ; Travia, A ; Amato, GMinerva pediatrica, 1997-09, Vol.49 (9), p.425-427ItalyTexto completo disponível |
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Material Type: Artigo
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Turner syndrome. Cytogenetic analysis of 165 patients with Turner syndrome. 1st reportVignetti, P ; Brinchi, V ; Bruni, L ; Rizzuti, A ; Tarani, L ; Tozzi, M CMinerva pediatrica, 1990-01, Vol.42 (1-2), p.25-27ItalyTexto completo disponível |
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Material Type: Artigo
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Cockayne's syndrome (study of 2 cases)Lanzi, G ; Calligaro, A ; Danesino, C ; Burgio, F R ; Verri, A PMinerva pediatrica, 1976-08, Vol.28 (26), p.1597-1608ItalyTexto completo disponível |
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Material Type: Artigo
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A case of partial 9p monosomyMonteverde, R ; Gimelli, G ; Cuoco, C ; Porta, S ; Lattere, MMinerva pediatrica, 1983-11, Vol.35 (22), p.1133-1136ItalyTexto completo disponível |