Bruno I - Search Results

1

Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children.

Calligaris L, Cortellazzo Wiel L, Sartor E, Berti I, Bruno I, Barbi E, Magnolato A. Calligaris L, et al. Among authors: bruno i. Am J Med Genet A. 2021 Dec;185(12):3895-3896. doi: 10.1002/ajmg.a.62420. Epub 2021 Jul 12. Am J Med Genet A. 2021. PMID: 34250743 Free article. No abstract available.

2

Deep sedation with propofol by nonanesthesiologists: a prospective pediatric experience.

Barbi E, Gerarduzzi T, Marchetti F, Neri E, Verucci E, Bruno I, Martelossi S, Zanazzo G, Sarti A, Ventura A. Barbi E, et al. Among authors: bruno i. Arch Pediatr Adolesc Med. 2003 Nov;157(11):1097-103. doi: 10.1001/archpedi.157.11.1097. Arch Pediatr Adolesc Med. 2003. PMID: 14609901

3

Mass screening for coeliac disease using antihuman transglutaminase antibody assay.

Tommasini A, Not T, Kiren V, Baldas V, Santon D, Trevisiol C, Berti I, Neri E, Gerarduzzi T, Bruno I, Lenhardt A, Zamuner E, Spanò A, Crovella S, Martellossi S, Torre G, Sblattero D, Marzari R, Bradbury A, Tamburlini G, Ventura A. Tommasini A, et al. Among authors: bruno i. Arch Dis Child. 2004 Jun;89(6):512-5. doi: 10.1136/adc.2003.029603. Arch Dis Child. 2004. PMID: 15155392 Free PMC article.

4

Widening sedation availability.

Barbi E, Bruno I, Ventura A. Barbi E, et al. Among authors: bruno i. J Pediatr. 2005 Mar;146(3):438-9; author reply 439. doi: 10.1016/j.jpeds.2004.09.016. J Pediatr. 2005. PMID: 15756247 No abstract available.

5

Attitudes of children with leukemia toward repeated deep sedations with propofol.

Barbi E, Badina L, Marchetti F, Vecchi R, Giuseppin I, Bruno I, Zanazzo G, Sarti A, Ventura A. Barbi E, et al. Among authors: bruno i. J Pediatr Hematol Oncol. 2005 Dec;27(12):639-43. doi: 10.1097/01.mph.0000193474.06870.9c. J Pediatr Hematol Oncol. 2005. PMID: 16344667

6

IBD and IBD mimicking enterocolitis in children younger than 2 years of age.

Cannioto Z, Berti I, Martelossi S, Bruno I, Giurici N, Crovella S, Ventura A. Cannioto Z, et al. Among authors: bruno i. Eur J Pediatr. 2009 Feb;168(2):149-55. doi: 10.1007/s00431-008-0721-2. Epub 2008 Jun 11. Eur J Pediatr. 2009. PMID: 18546019

7

A red baby should not be taken too lightly.

Faletra F, Bruno I, Berti I, Pastore S, Pirrone A, Tommasini A. Faletra F, et al. Among authors: bruno i. Acta Paediatr. 2012 Dec;101(12):e573-7. doi: 10.1111/apa.12018. Epub 2012 Sep 23. Acta Paediatr. 2012. PMID: 22946961

8

Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis.

Faletra F, Berti I, Tommasini A, Pecile V, Cleva L, Alberini E, Bruno I, Gasparini P. Faletra F, et al. Among authors: bruno i. Dermatology. 2012;225(4):294-7. doi: 10.1159/000342884. Epub 2012 Oct 24. Dermatology. 2012. PMID: 23095783 Free article.

9

Efficacy of clonidine in hyperammonemia induced hyperexcitability syndrome.

Calligaris L, Vidoni A, Bruno I, Vidoni M, Barbi E. Calligaris L, et al. Among authors: bruno i. Paediatr Anaesth. 2013 Feb;23(2):202-4. doi: 10.1111/pan.12088. Paediatr Anaesth. 2013. PMID: 23289776 No abstract available.

10

Autosomal recessive Stickler syndrome due to a loss of function mutation in the COL9A3 gene.

Faletra F, D'Adamo AP, Bruno I, Athanasakis E, Biskup S, Esposito L, Gasparini P. Faletra F, et al. Among authors: bruno i. Am J Med Genet A. 2014 Jan;164A(1):42-7. doi: 10.1002/ajmg.a.36165. Epub 2013 Nov 22. Am J Med Genet A. 2014. PMID: 24273071

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