منابع مشابه
Expandable DNA Repeat and Human Hereditary Disorders
Background & Aims: Nearly 30 hereditary disorders in humans result from an increase in the number of copies of simple repeats in genomic DNA, including fragile X syndrome, myotonic dystrophy, Huntington’s disease, and Friedreich’s ataxia. One the most frequently occurring types of mutation is trinucleotide repeat expansion. The present study was conducted with the aim of investigating the cause...
متن کاملA Comparison of the Effectiveness of Cognitive Bias Modification in Real and Placebo Conditions on Attentional Bias and Approach Bias in Opium Abusers
Background & Aim: Inability to control drug use is considered a core aspect of drug dependency. Part of this inability is due to cognitive biases resulting from individuals’ constant usage of drugs. The aim of the present study was to compare the effectiveness of cognitive bias modification in real and placebo conditions on attentional bias and approach bias in opium abusers. Methods: This stud...
متن کاملhereditary ataxia
the hereditary ataxias comprise a wide spectrum of heterogeneous disorders that share three features: ataxia, involvement of cerebellum or its connections, and heritability. in many hereditary ataxias, the underlying gene mutations have been identified. knowledge of the causative mutations allows a rational classification of hereditary ataxias as autosomal recessive, autosomal dominant or mater...
متن کاملThe Effect of Cognitive Bias Modification in the Attention Bias of Students With Test Anxiety
Abstract Introduction: Many of the students chr('39')educational problems, including academic failure and maladaptive behaviors, stem from exam anxiety caused by studentschr('39') cognitive bias. Cognitive bias modification can reduce attention biases students to be negative. Therefore, the purpose of the present study was to investigate the effectiveness of cognitive bias modification interven...
متن کاملHereditary chin trembling or hereditary chin myoclonus?
Hereditary chin trembling is a rare autosomal dominant disease often considered as an "essential tremor variant". The clinical and neurophysiological data obtained in a new white family lead to the suggestion that this abnormal involuntary movement is a focal variant of hereditary essential myoclonus.
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ژورنال
عنوان ژورنال: Nature
سال: 1993
ISSN: 0028-0836,1476-4687
DOI: 10.1038/362594a0