Clementi M - Search Results

1

Evaluation of LRRK2 G2019S penetrance: relevance for genetic counseling in Parkinson disease.

Goldwurm S, Zini M, Mariani L, Tesei S, Miceli R, Sironi F, Clementi M, Bonifati V, Pezzoli G. Goldwurm S, et al. Among authors: clementi m. Neurology. 2007 Apr 3;68(14):1141-3. doi: 10.1212/01.wnl.0000254483.19854.ef. Epub 2007 Jan 10. Neurology. 2007. PMID: 17215492

2

Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests.

Botta A, Tacconelli A, Bagni I, Giardina E, Bonifazi E, Pietropolli A, Clementi M, Novelli G. Botta A, et al. Among authors: clementi m. Neurology. 2005 Nov 22;65(10):1631-5. doi: 10.1212/01.wnl.0000184506.61354.5b. Neurology. 2005. PMID: 16301493

3

CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis.

Bruson A, Sambataro F, Querin G, D'Ascenzo C, Palmieri A, Agostini J, Gaiani A, Angelini C, Galbiati M, Poletti A, Pennuto M, Pegoraro E, Clementi M, Soraru G. Bruson A, et al. Among authors: clementi m. Eur J Neurol. 2012 Oct;19(10):1373-5. doi: 10.1111/j.1468-1331.2011.03646.x. Epub 2012 Jan 10. Eur J Neurol. 2012. PMID: 22233359

4

ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion.

Sorarù G, Clementi M, Forzan M, Orsetti V, D'Ascenzo C, Querin G, Palmieri A, Ermani M, Angelini C, Pegoraro E. Sorarù G, et al. Among authors: clementi m. Neurology. 2011 Jun 7;76(23):2030-1. doi: 10.1212/WNL.0b013e31821e557a. Neurology. 2011. PMID: 21646631 No abstract available.

5

Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America.

Bassi MT, Bergen AA, Bitoun P, Charles SJ, Clementi M, Gosselin R, Hurst J, Lewis RA, Lorenz B, Meitinger T, Messiaen L, Ramesar RS, Ballabio A, Schiaffino MV. Bassi MT, et al. Among authors: clementi m. Hum Genet. 2001 Jan;108(1):51-4. doi: 10.1007/s004390000440. Hum Genet. 2001. PMID: 11214907

6

Genetic susceptibility to infectious diseases.

Clementi M, Di Gianantonio E. Clementi M, et al. Reprod Toxicol. 2006 May;21(4):345-9. doi: 10.1016/j.reprotox.2005.08.006. Epub 2005 Oct 25. Reprod Toxicol. 2006. PMID: 16253476 Review.

7

Searching for psoriasis susceptibility genes in Italy: genome scan and evidence for a new locus on chromosome 1.

Capon F, Novelli G, Semprini S, Clementi M, Nudo M, Vultaggio P, Mazzanti C, Gobello T, Botta A, Fabrizi G, Dallapiccola B. Capon F, et al. Among authors: clementi m. J Invest Dermatol. 1999 Jan;112(1):32-5. doi: 10.1046/j.1523-1747.1999.00471.x. J Invest Dermatol. 1999. PMID: 9886260 Free article.

8

Theoretical recurrence risks for cleft lip derived from a population of consecutive newborns.

Tenconi R, Clementi M, Turolla L. Tenconi R, et al. Among authors: clementi m. J Med Genet. 1988 Apr;25(4):243-6. doi: 10.1136/jmg.25.4.243. J Med Genet. 1988. PMID: 3367349 Free PMC article.

9

Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?

Toldo I, Bruson A, Casarin A, Salviati L, Boniver C, Sartori S, Montagna P, Battistella PA, Clementi M. Toldo I, et al. Among authors: clementi m. J Headache Pain. 2011 Aug;12(4):435-41. doi: 10.1007/s10194-011-0359-8. Epub 2011 Jun 29. J Headache Pain. 2011. PMID: 21713554 Free PMC article.

10

High-resolution melt as a screening method in autosomal dominant polycystic kidney disease (ADPKD).

Virzì GM, Bruson A, Corradi V, Gastaldon F, de Cal M, Donà M, Cruz DN, Clementi M, Ronco C. Virzì GM, et al. Among authors: clementi m. J Clin Lab Anal. 2014 Jul;28(4):328-34. doi: 10.1002/jcla.21689. Epub 2014 Mar 22. J Clin Lab Anal. 2014. PMID: 24658975 Free PMC article.

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