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Mostrati risultati da 1 a 20 di 23
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
An adult patient with 3-methylglutaconic aciduria type 1 and movement disorders 2022 Lerjefors, LBonato, GBertolin, CSalviati, LCarecchio, M + JOURNAL OF NEUROLOGY - -
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy 2022 Bello, LucaBertolin, CinziaPegoraro, ElenaSalviati, Leonardo + NATURE COMMUNICATIONS - -
Multiple acyl-COA dehydrogenase deficiency in elderly carriers 2020 Salviati L.Zordan R.Bertolin C.Rossi S. + JOURNAL OF NEUROLOGY - -
Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy 2020 Cinzia BertolinGianni SorarùElena PegoraroGianni Sorarù + NEUROBIOLOGY OF AGING - -
A novel KRT1 c.1433A>G p.(Glu478Gly) mutation in a newborn with epidermolytic ichthyosis. 2020 Francesca CaroppoElena CamaCinzia BertolinLeonardo SalviatiAnna Belloni Fortina + CLINICAL CASE REPORTS - -
Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study. 2018 Marcato S.Kleinbub J. R.Querin G.Pick E.Martinelli I.Bertolin C.Cipolletta S.Pegoraro ESorarù G.& Palmieri + SCIENTIFIC REPORTS - -
New FIG4 gene mutations causing aggressive ALS 2018 Bertolin C.Querin G.BOZZONI, VIRGINIAMartinelli I.De Bortoli M.Rampazzo A.Pegoraro E.Sorarù G. + EUROPEAN JOURNAL OF NEUROLOGY - -
The clinical spectrum of CASQ1-related myopathy 2018 Semplicini CBertolin CBello LPantic BVianello SCATAPANO, FRANCESCOGavassini BFPREVITERO, MARCOCalore CSorarù GMinervini GTosatto SCEStramare RPegoraro E. + NEUROLOGY - -
Non-neural phenotype of spinal and bulbar muscular atrophy: Results from a large cohort of Italian patients 2016 QUERIN, GIORGIABERTOLIN, CINZIAVOLPE, MARCOPEGORARO, ELENAFORESTA, CARLOSILVANO, MARIACORRADO, DOMENICOIAFRATE, MASSIMOANGELINI, LORENZOSARTORI, LEONARDOGAIANI, ALESSANDRABELLO, LUCASEMPLICINI, CLAUDIOERMANI, MARIOFERLIN, ALBERTOSORARU', GIANNIPALMIERI, ARIANNABRIANI, CHIARAPENNUTO, MARIA + JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY - -
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis 2016 BERTOLIN, CINZIASORARU', GIANNI + NATURE GENETICS - -
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype 2016 BERTOLIN, CINZIAQUERIN, GIORGIABELLO, LUCACAO, MICHELANGELOERMANI, MARIOPEGORARO, ELENASORARU', GIANNIPENNUTO, MARIA + EUROPEAN JOURNAL OF NEUROLOGY - -
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 2015 BERTOLIN, CINZIAQUERIN, GIORGIASORARU', GIANNI + JOURNAL OF NEUROLOGY - -
Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. 2011 BERTOLIN, CINZIAVETTORI, ANDREAPERINI, GIULIAMOSTACCIUOLO, MARIA LUISAVAZZA, GIOVANNI + JOURNAL OF HUMAN GENETICS - -
Novel mutations in the L1CAM gene support the complexity of L1 syndrome 2010 BERTOLIN, CINZIABOARETTO, FRANCESCASALVIATI, LEONARDOOCCHI, GIANLUCAVAZZA, GIOVANNI + JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Caratterizzazione genetico-molecolare di un campione di soggetti affetti da disturbi dello spettro schizofrenico/bipolare provenienti da Chioggia 2008 Bertolin, Cinzia - - -
Individuation of new mutations in L1CAM gene in patients with L1 diseases. 2008 BOARETTO, FRANCESCABERTOLIN, CINZIAVAZZA, GIOVANNIVETTORI, ANDREAMOSTACCIUOLO, MARIA LUISA + - - -
Novel MFN2 mutations and phenotypic variability in patients with Charcot-Marie-Tooth disease type 2A. 2007 BOARETTO, FRANCESCAVAZZA, GIOVANNIVETTORI, ANDREABERTOLIN, CINZIAMOSTACCIUOLO, MARIA LUISA + - - -
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 2007 VAZZA, GIOVANNIBERTOLIN, CINZIAVETTORI, ANDREABOARETTO, FRANCESCARAMPINELLI, SABINAPERINI, GIULIAMOSTACCIUOLO, MARIA LUISA + MOLECULAR PSYCHIATRY - -
Evaluation of linkage signals in a subset of families with high recurrence of schizophrenia and bipolar disorder originating from Chioggia 2007 BERTOLIN, CINZIAVAZZA, GIOVANNIVETTORI, ANDREABOARETTO, FRANCESCARAMPINELLI, SABINAPERINI, GIULIAMOSTACCIUOLO, MARIA LUISA + - - 3rd International meeting on genetics of complex diseases and isolated populations
Genetic inheritance of schizophrenia and bipolar disorder in an italian population isolate 2006 RAMPINELLI, SABINAPERINI, GIULIAVAZZA, GIOVANNIBERTOLIN, CINZIAMOSTACCIUOLO, MARIA LUISA + - - -
Mostrati risultati da 1 a 20 di 23
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