Sensi A - Search Results

1

Clinical and radiological evaluation in children with microtia.

Calzolari F, Garani G, Sensi A, Martini A. Calzolari F, et al. Among authors: sensi a. Br J Audiol. 1999 Oct;33(5):303-12. doi: 10.3109/03005369909090114. Br J Audiol. 1999. PMID: 10890145

2

Genetic syndromes involving hearing.

Martini A, Calzolari F, Sensi A. Martini A, et al. Among authors: sensi a. Int J Pediatr Otorhinolaryngol. 2009 Dec;73 Suppl 1:S2-12. doi: 10.1016/S0165-5876(09)70002-3. Int J Pediatr Otorhinolaryngol. 2009. PMID: 20114151 Review.

3

Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO family.

Sensi A, Cocchi G, Martini A, Garani G, Trevisi P, Calzolari E. Sensi A, et al. Clin Genet. 1996 Jun;49(6):300-2. doi: 10.1111/j.1399-0004.1996.tb03792.x. Clin Genet. 1996. PMID: 8884078

4

Familial occurrence of multiple pterygium syndrome: expression in a heterozygote of the recessive form or variability of the dominant form?

Prontera P, Sensi A, Merlo L, Garani G, Cocchi G, Calzolari E. Prontera P, et al. Among authors: sensi a. Am J Med Genet A. 2006 Oct 15;140(20):2227-30. doi: 10.1002/ajmg.a.31428. Am J Med Genet A. 2006. PMID: 16964621

5

LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.

Sensi A, Ceruti S, Trevisi P, Gualandi F, Busi M, Donati I, Neri M, Ferlini A, Martini A. Sensi A, et al. Am J Med Genet A. 2011 May;155A(5):1096-101. doi: 10.1002/ajmg.a.33962. Epub 2011 Apr 7. Am J Med Genet A. 2011. PMID: 21480479

6

Exploring the clinical and epidemiological complexity of GJB2-linked deafness.

Gualandi F, Ravani A, Berto A, Sensi A, Trabanelli C, Falciano F, Trevisi P, Mazzoli M, Tibiletti MG, Cristofari E, Burdo S, Ferlini A, Martini A, Calzolari E. Gualandi F, et al. Among authors: sensi a. Am J Med Genet. 2002 Sep 15;112(1):38-45. doi: 10.1002/ajmg.10621. Am J Med Genet. 2002. PMID: 12239718

7

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.

Sensi A, Prontera P, Buldrini B, Palma S, Aiello V, Gruppioni R, Calzolari E, Volinia S, Martini A. Sensi A, et al. Am J Med Genet A. 2008 Jan 1;146A(1):110-5. doi: 10.1002/ajmg.a.32059. Am J Med Genet A. 2008. PMID: 18074369

8

An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology.

Prontera P, Escande F, Cocchi G, Donti E, Martini A, Sensi A. Prontera P, et al. Among authors: sensi a. Genet Couns. 2008;19(4):397-402. Genet Couns. 2008. PMID: 19239083

9

A familial case of NOG -related symphalangism spectrum disorder due to a novel NOG variant.

Parmeggiani G, Gualandi F, Limarzi M, Ferlini A, Brotto D, Martini A, Sensi A. Parmeggiani G, et al. Among authors: sensi a. Clin Dysmorphol. 2022 Oct 1;31(4):185-190. doi: 10.1097/MCD.0000000000000427. Epub 2022 Jul 14. Clin Dysmorphol. 2022. PMID: 36004948 No abstract available.

10

[The size of reticulocytes in beta-thalassemic homozygotes].

Sensi A, Camerini G, Castaldi G, Bariani L, Martini A, Masotti M, Scorrano M, Menghi P. Sensi A, et al. Riv Emoter Immunoematol. 1984;31(2):130-40. Riv Emoter Immunoematol. 1984. PMID: 6536094 Italian. No abstract available.

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