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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.
Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism.
Quadri M, Fang M, Picillo M, Olgiati S, Breedveld GJ, Graafland J, Wu B, Xu F, Erro R, Amboni M, Pappatà S, Quarantelli M, Annesi G, Quattrone A, Chien HF, Barbosa ER; International Parkinsonism Genetics Network; Oostra BA, Barone P, Wang J, Bonifati V. Quadri M, et al. Hum Mutat. 2013 Sep;34(9):1208-15. doi: 10.1002/humu.22373. Epub 2013 Aug 6. Hum Mutat. 2013. PMID: 23804577
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
627 results