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Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families.
Aridon P, Tarantino P, Ragonese P, D'Amelio M, Cinturino A, Salemi G, Gagliardi M, Lo Re V, Scarpitta A, Gambardella A, Quattrone A, Annesi G, Savettieri G. Aridon P, et al. Among authors: gagliardi m. Mov Disord. 2012 Mar;27(3):460-1. doi: 10.1002/mds.24027. Epub 2011 Nov 14. Mov Disord. 2012. PMID: 22083836 No abstract available.
PCDH19 mutations in female patients from Southern Italy.
Gagliardi M, Annesi G, Sesta M, Tarantino P, Conti P, Labate A, Di Rosa G, Quattrone A, Gambardella A. Gagliardi M, et al. Seizure. 2015 Jan;24:118-20. doi: 10.1016/j.seizure.2014.08.010. Epub 2014 Aug 30. Seizure. 2015. PMID: 25218114 Free article.
An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate.
Quadri M, Yang X, Cossu G, Olgiati S, Saddi VM, Breedveld GJ, Ouyang L, Hu J, Xu N, Graafland J, Ricchi V, Murgia D, Guedes LC, Mariani C, Marti MJ, Tarantino P, Asselta R, Valldeoriola F, Gagliardi M, Pezzoli G, Ezquerra M, Quattrone A, Ferreira J, Annesi G, Goldwurm S, Tolosa E, Oostra BA, Melis M, Wang J, Bonifati V. Quadri M, et al. Among authors: gagliardi m. Neurogenetics. 2015 Jan;16(1):55-64. doi: 10.1007/s10048-014-0425-x. Epub 2014 Oct 8. Neurogenetics. 2015. PMID: 25294124
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
Mumoli L, Tarantino P, Michelucci R, Bianchi A, Labate A, Franceschetti S, Marini C, Striano P, Gagliardi M, Ferlazzo E, Sofia V, Pennese L, Annesi G, Aguglia U, Guerrini R, Zara F, Gambardella A; Genetic Commission, Italian League Against Epilepsy. Mumoli L, et al. Among authors: gagliardi m. Epilepsia. 2015 Apr;56(4):e40-3. doi: 10.1111/epi.12944. Epub 2015 Mar 6. Epilepsia. 2015. PMID: 25752200 Free article.
619 results