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List of works by Daniela Di Bella

5HT2C CYS23/SER23 polymorphism is not associated with obsessive–compulsive disorder

scientific article published on 01 February 1998

Adult-onset autosomal dominant leukodystrophy without early autonomic dysfunctions linked to lamin B1 duplication: a phenotypic variant ⬇️

scientific article published on May 17, 2013

An association study between 5-HTTLPR polymorphism, COMT polymorphism, and Tourette's syndrome

scientific article published on 01 December 2000

Antipanic efficacy of paroxetine and polymorphism within the promoter of the serotonin transporter gene

scientific article published in December 2005

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

scientific article

Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations

scientific article published in April 2005

Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients

article

Bulimia nervosa, 5-HTTLPR polymorphism and treatment response to four SSRIs: a single-blind study.

scientific article published in December 2004

CO2-Induced Panic Attacks: A Twin Study ⬇️

scientific article published on September 1, 1998

Case???control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa

article

Clinical and genetic characteristics of late-onset Huntington's disease

scientific article

Dopamine receptor D2 and D4 genes, GABA(A) alpha-1 subunit genes and response to lithium prophylaxis in mood disorders.

scientific article

Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.

scientific article published on 25 January 2016

Efficacy of Paroxetine in Depression Is Influenced by a Functional Polymorphism Within the Promoter of the Serotonin Transporter Gene

article

Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa

scientific article published on 27 June 2012

MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 Diseases.

scientific article published in May 2016

Mutational mechanisms inMFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutations

scientific article published on 01 December 2015

Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.

scientific article

No association between obsessive-compulsive disorder and the 5-HT(1Dbeta) receptor gene.

scientific article published in October 2002

Novel 5′-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorder

article

Novel and recurrent spastin mutations in a large series of SPG4 Italian families.

scientific article published on 25 August 2012

Obsessive-Compulsive Disorder, 5-HTTLPR polymorphism and treatment response.

scientific article published in January 2002

Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.

scientific article published on 15 May 2014

Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28.

scientific article published on 9 May 2014

Pendular nystagmus in hypomyelinating leukodystrophy.

scientific article published on 8 July 2013

Pleiotropic effects of spastin on neurite growth depending on expression levels

scientific article

Polymorphic MAO-A and 5-HT-Transporter Genes: Analysis of Interactions in Panic Disorder

article

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.

scientific article

SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study.

scientific article published on 17 April 2016

Self-esteem in remitted patients with mood disorders is not associated with the dopamine receptor D4 and the serotonin transporter genes

scientific article published in August 1998

Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.

scientific article

Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation

article

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