| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Gilberto Silva, Maria J Ribeiro, Gabriel N Costa, Inês Violante, Fabiana Ramos, Jorge Saraiva, Miguel Castelo-Branc. Peripheral Attentional Targets under Covert Attention Lead to Paradoxically Enhanced Alpha Desynchronization in Neurofibromatosis Type 1. PloS one. vol 11. issue 2. 2016-08-01. PMID:26881921. |
neurofibromatosis type-1 (nf1) is a neurodevelopmental disease often exhibiting attentional deficits and learning disabilities, and is considered to model similar impairments common in other neurodevelopmental disorders such as autism. |
2016-08-01 |
2023-08-13 |
human |
| Kristy A Anderson, Paul T Shattuck, Benjamin P Cooper, Anne M Roux, Mary Wagne. Prevalence and correlates of postsecondary residential status among young adults with an autism spectrum disorder. Autism : the international journal of research and practice. vol 18. issue 5. 2015-11-04. PMID:23996904. |
compared with young adults with other disability types (learning disabilities, intellectual disabilities, or emotional disturbances), those with an autism spectrum disorder were more likely to have lived with a parent or guardian and least likely ever to have lived independently since leaving high school. |
2015-11-04 |
2023-08-12 |
Not clear |
| Kristy A Anderson, Paul T Shattuck, Benjamin P Cooper, Anne M Roux, Mary Wagne. Prevalence and correlates of postsecondary residential status among young adults with an autism spectrum disorder. Autism : the international journal of research and practice. vol 18. issue 5. 2015-11-04. PMID:23996904. |
members of the autism spectrum disorder group were less likely to have ever lived elsewhere and more likely to live under supervision since leaving high school compared to persons with emotional disturbances and learning disabilities. |
2015-11-04 |
2023-08-12 |
Not clear |
| Da Yong Le. Roles of mTOR Signaling in Brain Development. Experimental neurobiology. vol 24. issue 3. 2015-09-28. PMID:26412966. |
the abnormalities in the activity of mtor and its downstream signaling molecules in neural stem cells result in severe defects of brain developmental processes causing a significant number of brain disorders, such as pediatric brain tumors, autism, seizure, learning disability and mental retardation. |
2015-09-28 |
2023-08-13 |
Not clear |
| Jodene Goldenring Fine, Kayla A Musielak, Margaret Semrud-Clikema. Smaller splenium in children with nonverbal learning disability compared to controls, high-functioning autism and ADHD. Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence. vol 20. issue 6. 2014-10-20. PMID:24215424. |
the current study investigated morphological differences in the corpus callosum in children ages 8 to 18 years old with nonverbal learning disability (nld; n = 19), high-functioning autism (hfa; n = 23), predominantly inattentive adhd (adhd:pi; n = 23), and combined type adhd (adhd:c; n = 25), as well as those demonstrating typical development (n = 57). |
2014-10-20 |
2023-08-12 |
Not clear |
| Hiroshi Marut. Herbal therapeutics that block the oncogenic kinase PAK1: a practical approach towards PAK1-dependent diseases and longevity. Phytotherapy research : PTR. vol 28. issue 5. 2014-06-19. PMID:23943274. |
over 35 years research on paks, rac/cdc42(p21)-activated kinases, comes of age, and in particular pak1 has been well known to be responsible for a variety of diseases such as cancer (mainly solid tumors), alzheimer's disease, acquired immune deficiency syndrome and other viral/bacterial infections, inflammatory diseases (asthma and arthritis), diabetes (type 2), neurofibromatosis, tuberous sclerosis, epilepsy, depression, schizophrenia, learning disability, autism, etc. |
2014-06-19 |
2023-08-12 |
caenorhabditis_elegans |
| João Rocha, Cátia Guerra, Renata Oliveira, Sofia Dória, Ricardo Rego, Maria José Rosa. Late-onset Lennox-Gastaut syndrome as a phenotype of 15q11.1q13.3 duplication. Epileptic disorders : international epilepsy journal with videotape. vol 14. issue 2. 2012-10-10. PMID:22576075. |
the clinical symptoms associated with chromosome 15q duplication syndrome manifest through a heterogeneous group of symptoms characterised by hypotonia, delay in motor skills and language development, cognitive and learning disabilities, autism spectrum disorder and refractory epilepsy. |
2012-10-10 |
2023-08-12 |
Not clear |
| Nira Mashal, Anat Kasire. Principal component analysis study of visual and verbal metaphoric comprehension in children with autism and learning disabilities. Research in developmental disabilities. vol 33. issue 1. 2012-05-14. PMID:22001558. |
principal component analysis study of visual and verbal metaphoric comprehension in children with autism and learning disabilities. |
2012-05-14 |
2023-08-12 |
Not clear |
| Nira Mashal, Anat Kasire. Thinking maps enhance metaphoric competence in children with autism and learning disabilities. Research in developmental disabilities. vol 32. issue 6. 2012-02-28. PMID:21985987. |
thinking maps enhance metaphoric competence in children with autism and learning disabilities. |
2012-02-28 |
2023-08-12 |
Not clear |
| Nira Mashal, Anat Kasire. Thinking maps enhance metaphoric competence in children with autism and learning disabilities. Research in developmental disabilities. vol 32. issue 6. 2012-02-28. PMID:21985987. |
the primary goal of the current study was to examine the ability of children with autism (asd) and children with learning disabilities (ld) to improve their metaphoric competence by an intervention program using "thinking maps". |
2012-02-28 |
2023-08-12 |
Not clear |
| Anthony J Griswold, Deqiong Ma, Stephanie J Sacharow, Joycelyn L Robinson, James M Jaworski, Harry H Wright, Ruth K Abramson, Helle Lybaek, Nina Øyen, Michael L Cuccaro, John R Gilbert, Margaret A Pericak-Vanc. A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis. Autism research : official journal of the International Society for Autism Research. vol 4. issue 3. 2011-12-05. PMID:21360829. |
while a similar deletion has previously been reported in a family with spherocytosis, severe learning disabilities, and mild mental retardation, this is the first implication of chr14q23.2-23.3 in the etiology of autism and points to mthfd1, plekhg3, and churc1 as potential candidate genes contributing to autism risk. |
2011-12-05 |
2023-08-12 |
human |
| Aiden P Corvi. Neuronal cell adhesion genes: Key players in risk for schizophrenia, bipolar disorder and other neurodevelopmental brain disorders? Cell adhesion & migration. vol 4. issue 4. 2011-06-21. PMID:20574149. |
disruption of a number of these genes (including nrxn1, cntnap2 and cask) are known to cause diverse neurodevelopmental brain disorder phenotypes including schizophenia, autism, learning disability and specific language disorder. |
2011-06-21 |
2023-08-12 |
Not clear |
| Alistair T Pagnamenta, Hameed Khan, Susan Walker, Dianne Gerrelli, Kirsty Wing, Maria Clara Bonaglia, Roberto Giorda, Tom Berney, Elisa Mani, Massimo Molteni, Dalila Pinto, Ann Le Couteur, Joachim Hallmayer, James S Sutcliffe, Peter Szatmari, Andrew D Paterson, Stephen W Scherer, Veronica J Vieland, Anthony P Monac. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of medical genetics. vol 48. issue 1. 2011-06-10. PMID:20972252. |
rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (cdh8) in susceptibility to autism and learning disability. |
2011-06-10 |
2023-08-12 |
Not clear |
| Holly N Cukier, Raquel Rabionet, Ioanna Konidari, Melissa Y Rayner-Evans, Mary L Baltos, Harry H Wright, Ruth K Abramson, Eden R Martin, Michael L Cuccaro, Margaret A Pericak-Vance, John R Gilber. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. Neurogenetics. vol 11. issue 3. 2010-09-24. PMID:19921286. |
misregulation of the methyl-cpg-binding protein 2 (mecp2) gene has been found to cause a myriad of neurological disorders including autism, mental retardation, seizures, learning disabilities, and rett syndrome. |
2010-09-24 |
2023-08-12 |
Not clear |
| Alex Y Chen, Sue E Kim, Amy J Houtrow, Paul W Newachec. Prevalence of obesity among children with chronic conditions. Obesity (Silver Spring, Md.). vol 18. issue 1. 2010-03-31. PMID:19521350. |
we found that the prevalence of obesity among children 10-17 years of age without a chronic condition was 12.2% (95% confidence interval (ci) 11.5-13.0); the prevalence of obesity for children with asthma was 19.7% (19.5-19.9); with a hearing/vision condition was 18.4% (18.2-18.5); with learning disability was 19.3% (19.2-19.4); with autism was 23.4% (23.2-23.6); and with attention-deficit/hyperactivity disorder was 18.9% (18.7-19.0). |
2010-03-31 |
2023-08-12 |
human |
| Caleb Webber, Jayne Y Hehir-Kwa, Duc-Quang Nguyen, Bert B A de Vries, Joris A Veltman, Chris P Pontin. Forging links between human mental retardation-associated CNVs and mouse gene knockout models. PLoS genetics. vol 5. issue 6. 2009-09-30. PMID:19557186. |
rare copy number variants (cnvs) are frequently associated with common neurological disorders such as mental retardation (mr; learning disability), autism, and schizophrenia. |
2009-09-30 |
2023-08-12 |
mouse |
| Holly N Cukier, Alma M Perez, Ann L Collins, Zhaolan Zhou, Huda Y Zoghbi, Juan Bota. Genetic modifiers of MeCP2 function in Drosophila. PLoS genetics. vol 4. issue 9. 2008-11-11. PMID:18773074. |
loss of function of mecp2, a transcriptional regulator involved in chromatin remodeling, causes classic rett syndrome (rtt) as well as other related conditions characterized by autism, learning disabilities, or mental retardation. |
2008-11-11 |
2023-08-12 |
human |
| Louise Barnard, Kevin Muldoon, Reem Hasan, Gregory O'Brien, Mary Stewar. Profiling executive dysfunction in adults with autism and comorbid learning disability. Autism : the international journal of research and practice. vol 12. issue 2. 2008-08-01. PMID:18308763. |
we examined differences in executive function between 20 adults with autism and learning disability and 23 individuals with learning disabilities outside the autistic spectrum. |
2008-08-01 |
2023-08-12 |
human |
| Marleen Vanvuchelen, Herbert Roeyers, Willy De Weerd. Nature of motor imitation problems in school-aged males with autism: how congruent are the error types? Developmental medicine and child neurology. vol 49. issue 1. 2007-02-15. PMID:17209969. |
fifty-five males (eight low-functioning with autism: mean age 6y 2mo [sd 7.6mo]; 13 low-functioning with learning disabilities: mean age 6y 3mo [sd 2.8mo]; 17 high-functioning with autism: mean age 8y 9mo [sd 11mo]; and 17 typically developing: mean age 8y 8mo [sd 11.6mo]) were assessed on 18 single gestures and six sequences of hand postures. |
2007-02-15 |
2023-08-12 |
human |
| C Feroz-Nainar, P Selvaraj, Meera Ro. Risperidone induced oedema in a child with learning disability and autism. Autism : the international journal of research and practice. vol 10. issue 3. 2006-08-28. PMID:16682401. |
risperidone induced oedema in a child with learning disability and autism. |
2006-08-28 |
2023-08-12 |
Not clear |