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au.\*:("DI BELLA, Daniela")

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Results 1 to 13 of 13

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No association between obsessive-compulsive disorder and the 5-HT1Dβ receptor geneDI BELLA, Daniela; CAVALLINI, Maria Cristina; BELLODI, Laura et al.The American journal of psychiatry. 2002, Vol 159, Num 10, pp 1783-1785, issn 0002-953XArticle

An association study between 5-HTTLPR polymorphism, COMT polymorphism, and Tourette's syndromeCAVALLINI, Maria Cristina; DI BELLA, Daniela; CATALANO, Marco et al.Psychiatry research. 2000, Vol 97, Num 2-3, pp 93-100, issn 0165-1781Article

Lack of relationship between CO2 reactivity and serotonin transporter gene regulatory region polymorphism in panic disorderPERNA, Giampaolo; DI BELLA, Daniela; FAVARON, Elisa et al.American journal of medical genetics. 2004, Vol 129B, Num 1, pp 41-43, issn 0148-7299, 3 p.Article

Exploratory factor analysis of obsessive-compulsive patients and association with 5-HTTLPR polymorphismCAVALLINI, Maria Cristina; DI BELLA, Daniela; SILIPRANDI, Francesca et al.American journal of medical genetics. 2002, Vol 114, Num 3, pp 347-353, issn 0148-7299Article

Antipanic efficacy of paroxetine and polymorphism within the promoter of the serotonin transporter genePERNA, Giampaolo; FAVARON, Elisa; DI BELLA, Daniela et al.Neuropsychopharmacology (New York, NY). 2005, Vol 30, Num 12, pp 2230-2235, issn 0893-133X, 6 p.Article

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome I8pl I.22-qII.2CAGNOLI, Claudia; MARIOTTI, Caterina; DI DONATO, Stefano et al.Brain. 2006, Vol 129, pp 235-242, issn 0006-8950, 8 p., 1Article

Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48PENSATO, Viviana; CASTELLOTTI, Barbara; MORONI, Isabella et al.Brain. 2014, Vol 137, pp 1907-1920, issn 0006-8950, 14 p., 7Article

Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patientsCASTELLOTTI, Barbara; MARIOTTI, Caterina; PAREYSON, Davide et al.Neurogenetics (Oxford. Print). 2011, Vol 12, Num 3, pp 193-201, issn 1364-6745, 9 p.Article

Pleiotropic effects of spastin on neurite growth depending on expression levelsRIANO, Elena; MARTIGNONI, Monica; CAPPELLETTI, Graziella et al.Journal of neurochemistry. 2009, Vol 108, Num 5, pp 1277-1288, issn 0022-3042, 12 p.Article

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populationsRIBASES, Marta; GRATACOS, Monica; FOULON, Christine et al.European journal of human genetics. 2005, Vol 13, Num 4, pp 428-434, issn 1018-4813, 7 p.Article

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populationsRIBASES, Marta; GRATACOS, Monica; FOULON, Christine et al.Human molecular genetics (Print). 2004, Vol 13, Num 12, pp 1205-1212, issn 0964-6906, 8 p.Article

Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28SMETS, Katrien; DECONINCK, Tine; PARIZEL, Paul M et al.Neurology. 2014, Vol 82, Num 23, pp 2092-2100, issn 0028-3878, 9 p.Article

Erythropoietin in Friedreich Ataxia: No Effect on Frataxin in a Randomized Controlled TrialMARIOTTI, Caterina; FANCELLU, Roberto; TARONI, Franco et al.Movement disorders. 2012, Vol 27, Num 3, pp 446-449, issn 0885-3185, 4 p.Article

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