Literature DB >> 22383514

Intellectual disability (mental retardation).

Sarah E Shea1.   

Abstract

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Mesh：

Year:  2012        PMID： 22383514     DOI： 10.1542/pir.33-3-110

Source DB:  PubMed          Journal:  Pediatr Rev        ISSN： 0191-9601


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  8 in total

1.  Head circumference at birth and intellectual disability: a nationwide cohort study.

Authors:  Kristina Aagaard; Niels B Matthiesen; Cathrine C Bach; René T Larsen; Tine B Henriksen
Journal:  Pediatr Res       Date:  2019-10-02       Impact factor: 3.756

2.  A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child.

Authors:  Makanko Komara; Aisha M Al-Shamsi; Salma Ben-Salem; Bassam R Ali; Lihadh Al-Gazali
Journal:  J Mol Neurosci       Date:  2015-06-09       Impact factor: 3.444

3.  Variants of the OLIG2 Gene are Associated with Cerebral Palsy in Chinese Han Infants with Hypoxic-Ischemic Encephalopathy.

Authors:  Liya Sun; Lei Xia; Mingtai Wang; Dengna Zhu; Yangong Wang; Dan Bi; Juan Song; Caiyun Ma; Chao Gao; Xiaoli Zhang; Yanyan Sun; Xiaoyang Wang; Changlian Zhu; Qinghe Xing
Journal:  Neuromolecular Med       Date:  2018-09-03       Impact factor: 3.843

Review 4.  Astrocyte: A Foe or a Friend in Intellectual Disability-Related Diseases.

Authors:  Busong Wang; Lu Zou; Min Li; Liang Zhou
Journal:  Front Synaptic Neurosci       Date:  2022-06-23

5.  Early neurodevelopment and self-reported adolescent symptoms of depression and anxiety in a National Canadian Cohort Study.

Authors:  C Rebecca North; T Cam Wild; Lonnie Zwaigenbaum; Ian Colman
Journal:  PLoS One       Date:  2013-02-20       Impact factor: 3.240

6.  Psychiatric disorders in offspring of childhood or adolescent central nervous system tumor survivors: a national cohort study.

Authors:  Wuqing Huang; Kristina Sundquist; Jan Sundquist; Jianguang Ji
Journal:  Cancer Med       Date:  2020-11-01       Impact factor: 4.452

7.  X-linked mental retardation-hypotonic facies syndrome: Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene.

Authors:  Fatemeh Shakarami; Mehdi Jahani; Zahra Nouri; Mohammad Amin Tabatabaiefar
Journal:  Mol Genet Genomic Med       Date:  2022-08-13       Impact factor: 2.473

8.  De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome 2: Case Report and Literature Review.

Authors:  Maria Anna Siano; Ilaria De Maggio; Roberta Petillo; Dario Cocciadiferro; Emanuele Agolini; Massimo Majolo; Antonio Novelli; Matteo Della Monica; Carmelo Piscopo
Journal:  Pediatr Rep       Date:  2022-03-11
  8 in total

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