Export 26 results:
Autore Titolo Tipo [ Anno(Desc)]
Filtri: Autore è Faletra, Flavio  [Clear All Filters]
2015
Lougaris V, Faletra F, Lanzi G, Vozzi D, Marcuzzi A, Valencic E, Piscianz E, Bianco AM, Girardelli M, Baronio M, Loganes C, Fasth A, Salvini F, Trizzino A, Moratto D, Facchetti F, Giliani S, Plebani A, Tommasini A. Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype. Clin Immunol 2015;159(1):33-6.
Gortani G, Faletra F, Bruno I, Berti I, Ventura A. "Blaschkoid dyspigmentation" in a child: don't forget fibroblast chromosomal analysis. J Pediatr 2015;166(2):490-90.e1.
Naviglio S, Bruno I, Zanus C, Faletra F, Ventura A. A brain and heart connection: X-linked periventricular heterotopia. J Pediatr 2015;166(3):776.
d'Apolito M, Pisanelli D, Faletra F, Giardino I, Gigante M, Pettoello-Mantovani M, Goulet O, Gasparini P, Campanozzi A. Genetic analysis of Italian patients with congenital tufting enteropathy. World J Pediatr 2015;
Morgan A, Gandin I, Belcaro C, Palumbo P, Palumbo O, Biamino E, Dal Col V, Laurini E, Pricl S, Bosco P, Carella M, Ferrero GBattista, Romano C, d'Adamo APio, Faletra F, Vozzi D. Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability. Mutat Res 2015;781:32-6.
Bianco AMonica, Faletra F, Vozzi D, Girardelli M, Knowles A, Tommasini A, Zauli G, Marcuzzi A. Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Mol Med Rep 2015;12(4):6128-32.

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