Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

115 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.
Robusto M, Fang M, Asselta R, Castorina P, Previtali SC, Caccia S, Benzoni E, De Cristofaro R, Yu C, Cesarani A, Liu X, Li W, Primignani P, Ambrosetti U, Xu X, Duga S, Soldà G. Robusto M, et al. Among authors: cesarani a. Eur J Hum Genet. 2015 Jun;23(6):766-73. doi: 10.1038/ejhg.2014.168. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182139 Free PMC article.
Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss.
Primignani P, Trotta L, Castorina P, Lalatta F, Sironi F, Radaelli C, Degiorgio D, Curcio C, Travi M, Ambrosetti U, Cesarani A, Garavelli L, Formigoni P, Milani D, Murri A, Cuda D, Coviello DA. Primignani P, et al. Among authors: cesarani a. Genet Test Mol Biomarkers. 2009 Apr;13(2):209-17. doi: 10.1089/gtmb.2008.0086. Genet Test Mol Biomarkers. 2009. PMID: 19371219
Audiological findings in Williams syndrome: a study of 69 patients.
Barozzi S, Soi D, Comiotto E, Borghi A, Gavioli C, Spreafico E, Gagliardi C, Selicorni A, Forti S, Ambrosetti U, Cesarani A, Brambilla D. Barozzi S, et al. Among authors: cesarani a. Am J Med Genet A. 2012 Apr;158A(4):759-71. doi: 10.1002/ajmg.a.35241. Epub 2012 Mar 12. Am J Med Genet A. 2012. PMID: 22411878
Chronic cerebrospinal venous insufficiency in Ménière disease.
Di Berardino F, Alpini DC, Bavera PM, Cecconi P, Farabola M, Mattei V, Ambrosetti U, Cesarani A. Di Berardino F, et al. Among authors: cesarani a. Phlebology. 2015 May;30(4):274-9. doi: 10.1177/0268355514526871. Epub 2014 Mar 4. Phlebology. 2015. PMID: 24594584
Allergic contact dermatitis to hearing aids: literature and case reports.
Di Berardino F, Pigatto PD, Ambrosetti U, Cesarani A. Di Berardino F, et al. Among authors: cesarani a. Contact Dermatitis. 2009 May;60(5):291-3. doi: 10.1111/j.1600-0536.2009.01529.x. Contact Dermatitis. 2009. PMID: 19397624 Review. No abstract available.
115 results