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PEMEROLEHAN BAHASA SISWA TUNAGRAHITA KELAS VI SD [PDF]

Retorika, 2018
:  Language Acquisition of Mental Retardation Students at 6th Grade Elementary School. The aim of this research is to explain the comparison of vocabulary acquisition between student with severe mental retardation and student with mild mental retardation.
Reza Pandudinata, Sumarlam Sumarlam, Kundharu Saddhono   +2 more
doaj   +4 more sources

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

Human Mutation, 2010
Mental retardation affects 2‐3% of the population and shows a high heritability. Neurodevelopmental disorders that include pronounced impairment in language and speech skills occur less frequently.
Anthony P Monaco, Connie R Bezzina, Andre Franke   +2 more
exaly   +2 more sources

The role of fragile X mental retardation protein in major mental disorders

Neuropharmacology, 2011
S Hossein Fatemi
exaly   +2 more sources

LOX-1 mediates inflammatory activation of microglial cells through the p38-MAPK/NF-κB pathways under hypoxic-ischemic conditions

Cell Communication and Signaling, 2023
Background Microglial cells play an important role in the immune system in the brain. Activated microglial cells are not only injurious but also neuroprotective.
Yoshinori Aoki, Hongmei Dai, Fumika Furuta, Tomohisa Akamatsu, Takuya Oshima, Naoto Takahashi, Yu-ichi Goto, Akira Oka, Masayuki Itoh   +8 more
doaj   +1 more source

Duplication within two regions distal to MECP2: clinical similarity with MECP2 duplication syndrome

BMC Medical Genomics, 2023
Background X-linked methyl-CpG-binding protein 2 (MECP2) duplication syndrome is prevalent in approximately 1% of X-linked intellectual disabilities. Accumulating evidence has suggested that MECP2 is the causative gene of MECP2 duplication syndrome.
Keiko Akahoshi, Eiji Nakagawa, Yu-ichi Goto, Ken Inoue   +3 more
doaj   +1 more source

Mental retardation [PDF]

The Indian Journal of Pediatrics, 2003
Mental retardation (MR) occurs in 2-3% of the general population. Prevalence of milder MR is seven to ten times more than severe MR. Cause of severe MR can be determined in 60-70% of cases, as compared to mild MR where 35-55% remain idiopathic. The diagnostic process is aided considerably if the timing of a developmental insult can be determined ...
Madhulika, Kabra, Sheffali, Gulati
openaire   +3 more sources

Group Intensive Cognitive Activation in Patients with Major or Mild Neurocognitive Disorder

Frontiers in Behavioral Neuroscience, 2016
Background: No standard protocols are available for cognitive rehabilitation in conditions like Major or Mild Neurocognitive disorder (M-NCD or m-NCD, respectively); however, preliminary data seem to indicate that such interventions might have cost ...
Simonetta ePanerai, Domenica eTasca, Sabrina eMusso, Valentina eCatania, Federica eRuggeri, Alberto eRaggi, Stefano eMuratore, Giuseppina ePrestianni, Cinzia eBonforte, Raffaele eFerri   +9 more
doaj   +1 more source

LDOC1 expression in fibroblasts of patients with Down syndrome

Open Life Sciences, 2015
Down syndrome (DS) is characterised by intellectual disability and is caused by trisomy 21. Apoptosis is a programmed cell death process and is involved in neurodegenerative diseases such as Alzheimer.
Salemi Michele, Barone Concetta, Romano Carmelo, Caniglia Salvatore, Ragalmuto Alda, Scillato Francesco, Salluzzo Maria Grazia, Scavuzzo Cataldo, Vinci Mirella, Salluzzo Roberto, Romano Corrado, Bosco Paolo   +11 more
doaj   +1 more source

Defending Categorical Exemptions to the Death Penalty: Reflections on the ABA’s Resolutions Concerning the Execution of Juveniles and Persons with Mental Retardation [PDF]

, 1998
Steiker and Steiker discuss the ABA\u27s resolutions regarding the execution of juveniles and persons with mental retardation. The strongest legal case for the ABA\u27s position requires a more nuanced argument than the ABA has ...
Steiker, Carol, Steiker, Jordan
core   +2 more sources

Fragile X mental retardation protein controls synaptic vesicle exocytosis by modulating N-type calcium channel density

Nature Communications, 2014
Fragile X syndrome (FXS), the most common heritable form of mental retardation, is characterized by synaptic dysfunction. Synaptic transmission depends critically on presynaptic calcium entry via voltage-gated calcium (CaV) channels.
L. Ferron, M. Nieto-Rostro, J. Cassidy, A. Dolphin   +3 more
semanticscholar   +1 more source