about
Obsessive-Compulsive Disorder, 5-HTTLPR polymorphism and treatment response.No association between obsessive-compulsive disorder and the 5-HT(1Dbeta) receptor gene.Dopamine receptor D2 and D4 genes, GABA(A) alpha-1 subunit genes and response to lithium prophylaxis in mood disorders.Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations.SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28.Novel and recurrent spastin mutations in a large series of SPG4 Italian families.Pendular nystagmus in hypomyelinating leukodystrophy.Bulimia nervosa, 5-HTTLPR polymorphism and treatment response to four SSRIs: a single-blind study.Antipanic efficacy of paroxetine and polymorphism within the promoter of the serotonin transporter gene.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.MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 Diseases.Pleiotropic effects of spastin on neurite growth depending on expression levels.Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings.Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations.SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study.Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.Self-esteem in remitted patients with mood disorders is not associated with the dopamine receptor D4 and the serotonin transporter genes.Case???control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosaNovel 5′-regulatory region polymorphisms of the 5-HT2C receptor gene: association study with panic disorderPolymorphic MAO-A and 5-HT-Transporter Genes: Analysis of Interactions in Panic DisorderMutational mechanisms inMFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsSubclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutationAtaxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patientsAn association study between 5-HTTLPR polymorphism, COMT polymorphism, and Tourette's syndromeEfficacy of Paroxetine in Depression Is Influenced by a Functional Polymorphism Within the Promoter of the Serotonin Transporter Gene5HT2C CYS23/SER23 polymorphism is not associated with obsessive–compulsive disorderClinical and genetic characteristics of late-onset Huntington's disease
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Daniela Di Bella
@ast
Daniela Di Bella
@en
Daniela Di Bella
@es
Daniela Di Bella
@nl
Daniela Di Bella
@sl
type
label
Daniela Di Bella
@ast
Daniela Di Bella
@en
Daniela Di Bella
@es
Daniela Di Bella
@nl
Daniela Di Bella
@sl
prefLabel
Daniela Di Bella
@ast
Daniela Di Bella
@en
Daniela Di Bella
@es
Daniela Di Bella
@nl
Daniela Di Bella
@sl
P1053
K-2270-2016
P106
P1153
7003903937
P21
P31
P3829
P496
0000-0003-0912-5136
P569
2000-01-01T00:00:00Z