NGF and BDNF in pediatrics syndromes

G Ferraguti, S Terracina, G Micangeli… - Neuroscience & …, 2023 - Elsevier
Neurotrophins (NTs) as nerve growth factor (NGF) and brain-derived neurotrophic factor
(BDNF) play multiple roles in different settings including neuronal development, function and …

[PDF][PDF] Discapacidad intelectual

X Ke, J Liu - Traducción De Irarrázaval, M., Martin, A., Prieto-Tagle …, 2017 - iacapap.org
Esta publicación está dirigida a profesionales en formación o con práctica en salud mental y
no para el público general. Las opiniones vertidas en este libro son de responsabilidad de …

Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models

CL Gatto, K Broadie - Frontiers in synaptic neuroscience, 2010 - frontiersin.org
Proper brain function requires stringent balance of excitatory and inhibitory synapse
formation during neural circuit assembly. Mutation of genes that normally sculpt and …

[HTML][HTML] Intellectual disability

K Lee, M Cascella, R Marwaha - 2019 - europepmc.org
Objectives: Summarize the epidemiology of intellectual disability. Outline the etiology of
intellectual disability. Explain the treatment considerations for patients with intellectual …

Hyperexcitability and homeostasis in fragile X syndrome

X Liu, V Kumar, NP Tsai, BD Auerbach - Frontiers in Molecular …, 2022 - frontiersin.org
Fragile X Syndrome (FXS) is a leading inherited cause of autism and intellectual disability,
resulting from a mutation in the FMR1 gene and subsequent loss of its protein product …

A metabolomic and systems biology perspective on the brain of the fragile X syndrome mouse model

L Davidovic, V Navratil, CM Bonaccorso… - Genome …, 2011 - genome.cshlp.org
Fragile X syndrome (FXS) is the first cause of inherited intellectual disability, due to the
silencing of the X-linked Fragile X Mental Retardation 1 gene encoding the RNA-binding …

[图书][B] The causes of epilepsy: common and uncommon causes in adults and children

SD Shorvon, F Andermann, R Guerrini - 2011 - books.google.com
Causation is an aspect of epilepsy neglected in the scientific literature and in the
conceptualization of epilepsy at a clinical and experimental level. It was to remedy this …

Epilepsy in four genetically determined syndromes of intellectual disability

HTT Leung, H Ring - Journal of Intellectual Disability Research, 2013 - Wiley Online Library
Background Epilepsy occurs with increased frequency in people with an intellectual
disability (ID) compared to the rest of the population. A variety of research has in recent …

Deletion of Fmr1 results in sex‐specific changes in behavior

SO Nolan, CD Reynolds, GD Smith… - Brain and …, 2017 - Wiley Online Library
Objective In this study, we used a systemic Fmr1 knockout in order to investigate both
genotype‐and sex‐specific differences across multiple measures of sociability, repetitive …

[PDF][PDF] Deficiência intelectual

X Ke, J Liu - IACAPAP e-Textbook of Child and adolescent mental …, 2015 - dislexia.org.br
Esta publicação destina-se a profissionais em treinamento ou prática em saúde mental e
não para o público em geral. As opiniões expressas são de responsabilidade dos autores e …