Bonato S - Search Results

1

Biliary atresia and Kabuki syndrome: another case with long-term follow-up.

Selicorni A, Colombo C, Bonato S, Milani D, Giunta AM, Bedeschi MF. Selicorni A, et al. Among authors: bonato s. Am J Med Genet. 2001 May 1;100(3):251. doi: 10.1002/ajmg.1253. Am J Med Genet. 2001. PMID: 11343312 No abstract available.

2

Cognitive assessment in primary biliary cirrhosis: a case-control study.

Floreani A, Marchiori M, Bonato S, Zucchetto M, Naccarato R, Chiaramonte M. Floreani A, et al. Among authors: bonato s. Am J Gastroenterol. 1995 Feb;90(2):250-3. Am J Gastroenterol. 1995. PMID: 7847295

3

Concentrated ascitic fluid reinfusion after cascade filtration in tense ascites.

Rossaro L, Graziotto A, Bonato S, Plebani M, van Thiel DH, Burlina A, Naccarato R, Salvagnini M. Rossaro L, et al. Among authors: bonato s. Dig Dis Sci. 1993 May;38(5):903-8. doi: 10.1007/BF01295918. Dig Dis Sci. 1993. PMID: 8482189 Clinical Trial.

4

Efficacy and safety of the stepped care medical treatment of ascites in liver cirrhosis: a randomized controlled clinical trial comparing two diets with different sodium content.

Bernardi M, Laffi G, Salvagnini M, Azzena G, Bonato S, Marra F, Trevisani F, Gasbarrini G, Naccarato R, Gentilini P. Bernardi M, et al. Among authors: bonato s. Liver. 1993 Jun;13(3):156-62. doi: 10.1111/j.1600-0676.1993.tb00624.x. Liver. 1993. PMID: 8336527 Clinical Trial.

5

The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2K.

Crimella C, Tonelli A, Airoldi G, Baschirotto C, D'Angelo MG, Bonato S, Losito L, Trabacca A, Bresolin N, Bassi MT. Crimella C, et al. Among authors: bonato s. J Med Genet. 2010 Oct;47(10):712-6. doi: 10.1136/jmg.2010.077909. Epub 2010 Aug 3. J Med Genet. 2010. PMID: 20685671

6

Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.

Crippa F, Panzeri C, Martinuzzi A, Arnoldi A, Redaelli F, Tonelli A, Baschirotto C, Vazza G, Mostacciuolo ML, Daga A, Orso G, Profice P, Trabacca A, D'Angelo MG, Comi GP, Galbiati S, Lamperti C, Bonato S, Pandolfo M, Meola G, Musumeci O, Toscano A, Trevisan CP, Bresolin N, Bassi MT. Crippa F, et al. Among authors: bonato s. Arch Neurol. 2006 May;63(5):750-5. doi: 10.1001/archneur.63.5.750. Arch Neurol. 2006. PMID: 16682546

7

Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin.

Airoldi G, Guidarelli A, Cantoni O, Panzeri C, Vantaggiato C, Bonato S, Grazia D'Angelo M, Falcone S, De Palma C, Tonelli A, Crimella C, Bondioni S, Bresolin N, Clementi E, Bassi MT. Airoldi G, et al. Among authors: bonato s. Neurogenetics. 2010 Feb;11(1):91-100. doi: 10.1007/s10048-009-0206-0. Epub 2009 Jul 11. Neurogenetics. 2010. PMID: 19593598

8

A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.

Romaniello R, Zucca C, Tonelli A, Bonato S, Baschirotto C, Zanotta N, Epifanio R, Righini A, Bresolin N, Bassi MT, Borgatti R. Romaniello R, et al. Among authors: bonato s. J Neurol Neurosurg Psychiatry. 2010 Aug;81(8):840-3. doi: 10.1136/jnnp.2008.163402. J Neurol Neurosurg Psychiatry. 2010. PMID: 20682717

9

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15.

Vantaggiato C, Crimella C, Airoldi G, Polishchuk R, Bonato S, Brighina E, Scarlato M, Musumeci O, Toscano A, Martinuzzi A, Santorelli FM, Ballabio A, Bresolin N, Clementi E, Bassi MT. Vantaggiato C, et al. Among authors: bonato s. Brain. 2013 Oct;136(Pt 10):3119-39. doi: 10.1093/brain/awt227. Epub 2013 Sep 11. Brain. 2013. PMID: 24030950 Free PMC article.

10

Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.

Del Bo R, Moggio M, Rango M, Bonato S, D'Angelo MG, Ghezzi S, Airoldi G, Bassi MT, Guglieri M, Napoli L, Lamperti C, Corti S, Federico A, Bresolin N, Comi GP. Del Bo R, et al. Among authors: bonato s. Neurology. 2008 Dec 9;71(24):1959-66. doi: 10.1212/01.wnl.0000327095.32005.a4. Epub 2008 Oct 22. Neurology. 2008. PMID: 18946002

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

94 results

Search Page

Filters