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17.992  Articles
1 of 1.800 pages  |  10  records  |  more records»
AbstractHealthy or not a person's life is not only based on physical but mental. Mental and physical health must be balanced to have a good life. Many people do not pay attention to their mental health and those around them so that their lives can no long... see more

A disorder of copper metabolism at Wilson’s disease (WD), conditioned by a mutation of adenosine thriphospate P-type gene (ATP7B), results in irreversible changes in the liver and in the nervous system. Mortality is high at WD, but it is one of hereditary... see more

A disorder of copper metabolism at Wilson’s disease (WD), conditioned by a mutation of adenosine thriphospate P-type gene (ATP7B), results in irreversible changes in the liver and in the nervous system. Mortality is high at WD, but it is one of hereditary... see more

This article describes the clinical forms of reproductive system in men and women related with different mutations. Mutations in the genes of FSH and its receptor in women, and in the genes of LH and its receptor in men are the most significant in reprodu... see more

Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to... see more

Autism spectrum disorders (ASD) are a complex group of developmental pathologies characterized by the disorders of social interaction and communication, along with repetitive restrictive behavior. Many factors are associated with the development of ASD, i... see more

INTRODUCTION: Hypertrichosis is a rare disorder in which there is an exaggerated growth of body hair in places that are not necessarily androgen-dependent, a particular feature of hirsutism. Its etiology is still questionable, with an increased incid... see more

Idiopathic restrictive cardiomyopathy (IRC) is a rare form of heart muscle disease. Genetic studies have revealed that in about half the cases, IRC forms part of the hereditary sarcomeric contractile protein disease spectrum. Mutations in several sarcomer... see more

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