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Autore [ Titolo(Desc)] Tipo Anno
Filtri: Autore è Bruno, Irene  [Clear All Filters]
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A
Faletra F, d'Adamo AP, Bruno I, Athanasakis E, Biskup S, Esposito L, Gasparini P. Autosomal recessive Stickler syndrome due to a loss of function mutation in the COL9A3 gene. Am J Med Genet A 2014;164A(1):42-7.
B
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.
C
Londero M, Pastore S, Zanazzo GA, Bruno I, Ventura A. A child with pain after mild trauma. J Pediatr 2010;157(4):693.
H
L'Imperio V, Bruno I, Rabach I, Smith A, Chinello C, Stella M, Magni F, Pagni F. Histoproteomic Characterization of Localized Cutaneous Amyloidosis in X-Linked Reticulate Pigmentary Disorder. Skin Pharmacol Physiol 2017;30(2):90-93.
L
Benelli E, Bruno I, Belcaro C, Ventura A, Berti I. Legius syndrome: case report and review of literature. Ital J Pediatr 2015;41:8.
M
Rabach I, Salis S, Bruno I, Ventura A. Macrocephaly and palmoplantar pitting. Arch Dis Child 2016;
N
Faletra F, d'Adamo APio, Pensiero S, Athanasakis E, Catalano D, Bruno I, Gasparini P. A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family. Ophthalmic Genet 2013;34(1-2):115-7.
R
Faletra F, Bruno I, Berti I, Pastore S, Pirrone A, Tommasini A. A red baby should not be taken too lightly. Acta Paediatr 2012;101(12):e573-7.
W
Da Lozzo P, Magnolato A, Del Rizzo I, Sirchia F, Bruno I, Barbi E. When Long-Lasting Food Selectivity Leads to an Unusual Genetic Diagnosis: A Case Report. J Adolesc Health 2019;64(1):137-138.

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