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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 1
1970 1
1973 1
1974 1
1975 1
1976 6
1977 2
1978 1
1979 7
1980 4
1981 4
1982 10
1983 12
1984 10
1985 8
1986 12
1987 8
1988 5
1989 17
1990 19
1991 11
1992 17
1993 18
1994 18
1995 24
1996 25
1997 14
1998 21
1999 17
2000 31
2001 29
2002 19
2003 28
2004 26
2005 30
2006 33
2007 44
2008 56
2009 49
2010 53
2011 65
2012 60
2013 76
2014 79
2015 78
2016 67
2017 69
2018 67
2019 90
2020 106
2021 112
2022 74
2023 61
2024 16

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1,497 results

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Quoted phrase not found in phrase index: "Intellectual disability, progressive"
Page 1
The natural history and prognosis of epilepsy.
Beghi E, Giussani G, Sander JW. Beghi E, et al. Epileptic Disord. 2015 Sep;17(3):243-53. doi: 10.1684/epd.2015.0751. Epileptic Disord. 2015. PMID: 26234761 Review.
Early response to treatment is an important positive predictor of long-term prognosis, while the history of a high number of seizures at the time of diagnosis, intellectual disability, and symptomatic aetiology are negative predictors. ...
Early response to treatment is an important positive predictor of long-term prognosis, while the history of a high number of seizures at the …
Myhre syndrome.
Le Goff C, Michot C, Cormier-Daire V. Le Goff C, et al. Clin Genet. 2014 Jun;85(6):503-13. doi: 10.1111/cge.12365. Epub 2014 Apr 2. Clin Genet. 2014. PMID: 24580733 Review.
Myhre syndrome (MS) is a developmental disorder characterized by typical facial dysmorphism, thickened skin, joint limitation and muscular pseudohypertrophy. Other features include brachydactyly, short stature, intellectual deficiency with behavioral problems and deafness. …
Myhre syndrome (MS) is a developmental disorder characterized by typical facial dysmorphism, thickened skin, joint limitation and muscular p …
Ageing in individuals with intellectual disability: issues and concerns in Hong Kong.
Tse MM, Kwan RY, Lau JL. Tse MM, et al. Hong Kong Med J. 2018 Feb;24(1):68-72. doi: 10.12809/hkmj166302. Epub 2018 Jan 12. Hong Kong Med J. 2018. PMID: 29326402 Free article. Review.
This paper aimed to explore the issues and concerns about individuals with intellectual disability as they age. METHODS: Articles that discussed people older than 30 years with an intellectual disability and those that identified ageing health issues a …
This paper aimed to explore the issues and concerns about individuals with intellectual disability as they age. METHODS: Artic …
Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy.
Iskandar K, Triono A, Sunartini, Dwianingsih EK, Indraswari BW, Kirana IR, Ivana G, Sutomo R, Patria SY, Herini ES, Gunadi. Iskandar K, et al. PLoS One. 2022 Oct 31;17(10):e0276640. doi: 10.1371/journal.pone.0276640. eCollection 2022. PLoS One. 2022. PMID: 36315559 Free PMC article.
INTRODUCTIONS: Duchenne muscular dystrophy (DMD) is an X-linked recessive progressive muscular disease marked by developmental delays due to mutations in the DMD gene, which encodes dystrophin. ...There were no DMD patients with ASD, while 4 boys (7.8%) had comorbid …
INTRODUCTIONS: Duchenne muscular dystrophy (DMD) is an X-linked recessive progressive muscular disease marked by developmental …
People with intellectual disability and employment sustainability: A qualitative interview study.
Helena T, Magnus T, Carin SN. Helena T, et al. J Appl Res Intellect Disabil. 2023 Jan;36(1):78-86. doi: 10.1111/jar.13036. Epub 2022 Sep 21. J Appl Res Intellect Disabil. 2023. PMID: 36129123 Free PMC article.
BACKGROUND: Swedish employment rates are disproportionately low among people with intellectual disability and research on employment sustainability in this group is scarce. This study investigated employment sustainability among people with intellectual di …
BACKGROUND: Swedish employment rates are disproportionately low among people with intellectual disability and research on empl …
Intellectual disability in paediatric patients with genetic muscle diseases.
Specht S, Straub V. Specht S, et al. Neuromuscul Disord. 2021 Oct;31(10):988-997. doi: 10.1016/j.nmd.2021.08.012. Neuromuscul Disord. 2021. PMID: 34736636 Review.
A significant consideration in assessing a patient with muscle weakness is the presence or absence of intellectual disability, thus narrowing the differential diagnostic approach in any child with an as yet undiagnosed muscle disease. ...It also summarises di …
A significant consideration in assessing a patient with muscle weakness is the presence or absence of intellectual disability, …
Fragile X and X-linked intellectual disability: four decades of discovery.
Lubs HA, Stevenson RE, Schwartz CE. Lubs HA, et al. Am J Hum Genet. 2012 Apr 6;90(4):579-90. doi: 10.1016/j.ajhg.2012.02.018. Am J Hum Genet. 2012. PMID: 22482801 Free PMC article. Review.
X-Linked intellectual disability (XLID) accounts for 5%-10% of intellectual disability in males. ...At the same time, it has improved the clinical diagnosis of XLID and allowed for carrier detection and prevention strategies through gamete donation, pr …
X-Linked intellectual disability (XLID) accounts for 5%-10% of intellectual disability in males. ...At the same …
Genetics of recessive cognitive disorders.
Musante L, Ropers HH. Musante L, et al. Trends Genet. 2014 Jan;30(1):32-9. doi: 10.1016/j.tig.2013.09.008. Epub 2013 Oct 28. Trends Genet. 2014. PMID: 24176302 Review.
Most severe forms of intellectual disability (ID) have specific genetic causes. Numerous X chromosome gene defects and disease-causing copy-number variants have been linked to ID and related disorders, and recent studies have revealed that sporadic cases are …
Most severe forms of intellectual disability (ID) have specific genetic causes. Numerous X chromosome gene defects and dise …
Neuroimaging Changes in Menkes Disease, Part 1.
Manara R, D'Agata L, Rocco MC, Cusmai R, Freri E, Pinelli L, Darra F, Procopio E, Mardari R, Zanus C, Di Rosa G, Soddu C, Severino M, Ermani M, Longo D, Sartori S; Menkes Working Group in the Italian Neuroimaging Network for Rare Diseases. Manara R, et al. AJNR Am J Neuroradiol. 2017 Oct;38(10):1850-1857. doi: 10.3174/ajnr.A5186. Epub 2017 May 11. AJNR Am J Neuroradiol. 2017. PMID: 28495946 Free PMC article. Review.
Menkes disease is a rare multisystem X-linked disorder of copper metabolism. ...In later phases of the disease, concomitant progressive neurodegeneration might hinder the myelination progression. ...
Menkes disease is a rare multisystem X-linked disorder of copper metabolism. ...In later phases of the disease, concomitant …
Dementia and mild cognitive impairment in adults with intellectual disability: issues of diagnosis.
Krinsky-McHale SJ, Silverman W. Krinsky-McHale SJ, et al. Dev Disabil Res Rev. 2013;18(1):31-42. doi: 10.1002/ddrr.1126. Dev Disabil Res Rev. 2013. PMID: 23949827 Review.
Individuals with intellectual disability (ID) are now living longer with the majority of individuals reaching middle and even "old age." ...Early diagnosis will continue to be of growing importance, both to support symptomatic treatment and to prevent irreversible n …
Individuals with intellectual disability (ID) are now living longer with the majority of individuals reaching middle and even …
1,497 results