Movement Disorders (revue) - Checkpoint (PubMed)

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List of bibliographic references

Number of relevant bibliographic references: 14.
Ident.Authors (with country if any)Title
000271 (2015) Giovanni Defazio [Italie] ; Mark Hallett ; Hyder A. Jinnah ; Glenn T. Stebbins ; Angelo F. Gigante ; Gina Ferrazzano ; Antonella Conte ; Giovanni Fabbrini ; Alfredo BerardelliDevelopment and validation of a clinical scale for rating the severity of blepharospasm.
000E27 (2012) Giovanni Defazio [Italie] ; Giovanni Abbruzzese ; Maria Stella Aniello ; Roberta Di Fede ; Marcello Esposito ; Giovanni Fabbrini ; Paolo Girlanda ; Rocco Liguori ; Lucio Marinelli ; Davide Martino ; Francesca Morgante ; Lucio Santoro ; Michele Tinazzi ; Alfredo BerardelliEye symptoms in relatives of patients with primary adult-onset dystonia.
000F54 (2012) Davide Martino [Italie] ; Alfredo Berardelli ; Giovanni Abbruzzese ; Anna Rita Bentivoglio ; Marcello Esposito ; Giovanni Fabbrini ; Arianna Guidubaldi ; Paolo Girlanda ; Rocco Liguori ; Lucio Marinelli ; Francesca Morgante ; Lucio Santoro ; Giovanni DefazioAge at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia.
001400 (2011) Davide Martino [Italie] ; Annabella Di Giorgio ; Enrico D'Ambrosio ; Teresa Popolizio ; Antonella Macerollo ; Paolo Livrea ; Alessandro Bertolino ; Giovanni DefazioCortical gray matter changes in primary blepharospasm: a voxel-based morphometry study.
001780 (2010) Francesco Roselli [Italie] ; Nicola M. Pisciotta ; Michele Pennelli ; Maria S. Aniello ; Angelo Gigante ; Maria F. De Caro ; Ermanno Ferrannini ; Bruno Tartaglione ; Artor Niccoli-Asabella ; Giovanni Defazio ; Paolo Livrea ; Giuseppe RubiniMidbrain SERT in degenerative parkinsonisms: a 123I-FP-CIT SPECT study.
001B69 (2009) Francesco Roselli [Italie] ; Nicola M. Pisciotta ; Robert Perneczky ; Michele Pennelli ; Maria S. Aniello ; Maria F. De Caro ; Ermanno Ferrannini ; Bruno Tartaglione ; Giovanni Defazio ; Giuseppe Rubini ; Paolo LivreaSeverity of neuropsychiatric symptoms and dopamine transporter levels in dementia with Lewy bodies: a 123I-FP-CIT SPECT study.
002408 (2008) Maria Stella Aniello [Italie] ; Davide Martino ; Vittoria Petruzzella ; Roberto Eleopra ; Michelangelo Mancuso ; Rosa Dell'Aglio ; Michele Cavallo ; Gabriele Siciliano ; Giovanni DefazioBilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation.
002972 (2007) Davide Martino [Italie] ; Giovanni Defazio ; Giovanni Abbruzzese ; Roberta Marchese ; Giovanni Fabbrini ; Venturino Decembrino ; Alfredo BerardelliAre nongenetic triggers for dystonia type-specific? A study exploring scoliosis in blepharospasm.
002F83 (2005) Davide Martino [Italie] ; Giovanni Defazio ; Giovanni Alessio ; Giovanni Abbruzzese ; Paolo Girlanda ; Michele Tinazzi ; Giovanni Fabbrini ; Lucio Marinelli ; Giovanni Majorana ; Maria Buccafusca ; Laura Vacca ; Paolo Livrea ; Alfredo BerardelliRelationship between eye symptoms and blepharospasm: a multicenter case-control study.
003151 (2005) Paolo Lamberti [Italie] ; Stefano Zoccolella ; Giovanni Iliceto ; Elio Armenise ; Angela Fraddosio ; Michele De Mari ; Paolo LivreaEffects of levodopa and COMT inhibitors on plasma homocysteine in Parkinson's disease patients.
003474 (2004) Marina De Tommaso [Italie] ; Nicola Specchio ; Vittorio Sciruicchio ; Olimpia Difruscolo ; Luigi Maria SpecchioEffects of rivastigmine on motor and cognitive impairment in Huntington's disease.
003778 (2003) Giovanni Defazio [Italie] ; Francesco Brancati ; Enza Maria Valente ; Viviana Caputo ; Antonio Pizzuti ; Davide Martino ; Giovanni Abbruzzese ; Paolo Livrea ; Alfredo Berardelli ; Bruno DallapiccolaFamilial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene.
003A99 (2002) Giovanni Defazio [Italie] ; Paolo LivreaEpidemiology of primary blepharospasm.
003D50 (2001) T. Perniola [Italie] ; L. Margari ; M G De Iaco ; A. Presicci ; P. Ventura ; E. Ferrannini ; G. IllicetoFamilial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance.

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