Brain Networks

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Brain networks connect levels of organization in the brain and link structure to function. Following some basic concepts of network theory and brain connectivity, this new area of  study in neuroscience aims to reveal principles of brain architecture and how structure is essential for a proper function. In this section you will find information about this new  approach and how brain networks can be affected by different neuropaediatric disorders.

Blue Consciouosness 1000

Blue Consciousness (2013)

http://www.plioplys.com/blue-consciousness.php

Copyright Audrius V.Plioplys 2013

THE HUMAN CONNECTOME

Building the brain map

New Insights on Human Connectome

ENVIRONMENTAL FACTORS

Adequate care for children protects their brain development

24 posts published about Brain networks

Synaptic metabolism course

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A course about synaptic metabolism of the Recordati Rare Disease Foundation will be held in Barcelona, Spain, on November 16 – 18, 2017. Participants are expected to have prior knowledge about the field: practical experience with diagnosis treatment, and/or basic research is recommended. Participants are also expected to present a case report relevant to the theme […]

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The gut-brain axis communication and its relationship with the neurological disorders

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“We are what we eat”. These well-known words, widely used by nutritionists, date back to Ludwig Feuerbach, a German philosopher of XIX century that focused on the needs of the human body to be properly fed, in contrast with the dominant way of thinking of his age that gave priority to feed the souls. May […]

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Genes, dopamine and creativity in everyday life

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The frescos of Sistine Chapel, Einstein’s Theory of Relativity, the unpredictable Leo Messi’s dribbles… these are only some examples of creativity at the highest level. But creativity is not only a prerogative of few “beautiful minds”. Every person in everyday life has to deal with common problems that require a certain dose of creativity to […]

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Rett syndrome: loss of balance between excitation and inhibition

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Rett syndrome (RTT) is a rare neurodevelopmental disease. Mutations in MECP2 (located on the X chromosome) are the most common cause. However, mutations in other genes such as CDKL5 and FOXG1 have been reported to produce a Rett-like phenotype. How these different genetic defects determine similar clinical features has yet to be elucidated. Italian researchers […]

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