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VAZZA GIOVANNI: PUBBLICAZIONI

1 Mostacciuolo ML, Rampoldi L, Righetti E, Vazza G, Schiavon F, Angelini C.
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity.
NEUROMUSCULAR DISORD. Oct 2000; 10(7): 497-502
2 Vazza G, Zortea M, Boaretto F, Micaglio GF, Sartori V, Mostacciuolo ML.
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.
AM J HUM GENET. Aug 2000; 67(2): 504-9
3 Zortea M, Vettori A, Trevisan CP, Bellini S, Vazza G, Armani M, Simonati A, Mostacciuolo ML.
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1.
J MED GENET. Jun 2002; 39(6): 387-90
4 Vazza G, Picelli S, Bozzato A, Mostacciuolo ML.
Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28.
GENE. Sep 2003; 314: 113-20
5 Soragna D, Vettori A, Carraro G, Marchioni E, Vazza G, Bellini S, Tupler R, Savoldi F, Mostacciuolo ML.
A locus for migraine without aura maps on chromosome 14q21.2-q22.3.
AM J HUM GENET. Jan 2003; 72(1): 161-7
6 Mostacciuolo M, Crestanello E, Boaretto F, Boscolo E, Liguori M, Tessarolo D, Vettori A, Vazza G.
Distal hereditary motor neuropathy (DHMN): a new locus for an autosomal recessive form.
J PERIPHER NERV SYST. Jun 2004; 9(2): 122-123
7 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.
Eight Novel Mutations in SPG4 in a Large Sample of Patients With Hereditary Spastic Paraplegia.
ARCH NEUROL-CHICAGO. May 2006; 63(5): 750-5
8 Vazza G, Bertolin C, Scudellaro E, Vettori A, Boaretto F, Rampinelli S, De Sanctis G, Perini G, Peruzzi P, Mostacciuolo ML.
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26.
MOL PSYCHIATR. Sep 2006
9 Vazza G, Merlini L, Bertolin C, Zortea M, Mostacciuolo ML.
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset.
NEUROMUSCULAR DISORD. DEC 2006; 16(12): 878-881
10 Muglia M, Vazza G, Patitucci A, Milani M, Pareyson D, Taroni F, Quattrone A, Mostacciuolo ML.
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy.
J NEUROL NEUROSUR PS. Nov 2007; 78(11): 1286-7
11 Michelucci R, Scudellaro E, Testoni S, Passarelli D, Riguzzi P, Diani E, Vazza G, Vianello V, Scabar A, Mostacciuolo ML, Volpi L, Rubboli G, Pinardi F, Mancardi MM, Tassinari CA, Nobile C.
Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci.
EPILEPSY RES. JUL 2008; 80(1): 9-17
12 Mostacciuolo ML, Pastorello E, Vazza G, Miorin M, Angelini C, Tomelleri G, Galluzzi G, Trevisan CP.
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample.
CLIN GENET. JUN 2009; 75(6): 550-555