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The American Journal of Psychiatry|October 3, 2002
No association between obsessive-compulsive disorder and the 5-HT(1Dbeta) receptor geneDaniela Di Bella, Maria Cristina Cavallini, Laura Bellodi
Neurogenetics|August 12, 2025
KIF1C-related disorders: spastic ataxia or hypomyelinating leukodystrophy? A paradigm of classification ambiguityChiara Benzoni, Marco Moscatelli, Daniela Di Bella, et al.
Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 28Caterina Mariotti, Daniela Di Bella, Stefano Di Donato, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 22, 2005
Antipanic efficacy of paroxetine and polymorphism within the promoter of the serotonin transporter geneGiampaolo Perna, Elisa Favaron, Daniela Di Bella, et al.
American Journal of Medical Genetics|March 29, 2002
Exploratory factor analysis of obsessive-compulsive patients and association with 5-HTTLPR polymorphismMaria Cristina Cavallini, Daniela Di Bella, Francesca Siliprandi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 27, 2004
Lack of relationship between CO2 reactivity and serotonin transporter gene regulatory region polymorphism in panic disorderGiampaolo Perna, Daniela di Bella, Elisa Favaron, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2021
Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotypeMarta Gatti, Stefania Magri, Daniela Di Bella, et al.
Cerebellum (London, England)|August 23, 2024
Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New CasesClaudia Ciaccio, Matilde Taddei, Chiara Pantaleoni, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literatureChiara Benzoni, Domenico Aquino, Daniela Di Bella, et al.
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