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

Year Number of Results
1977 1
1978 2
1980 1
1982 1
1983 1
1984 1
1985 1
1986 2
1987 3
1988 2
1990 4
1991 4
1993 2
1994 4
1995 5
1996 3
1998 6
1999 3
2000 3
2001 8
2002 3
2003 2
2004 5
2005 4
2006 7
2007 4
2008 6
2009 5
2010 7
2011 8
2012 7
2013 10
2014 8
2015 9
2016 7
2017 8
2018 7
2019 7
2020 3
2021 4
2022 6
2023 8
2024 3

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176 results

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Page 1
Niemann-Pick disease type C.
Vanier MT. Vanier MT. Orphanet J Rare Dis. 2010 Jun 3;5:16. doi: 10.1186/1750-1172-5-16. Orphanet J Rare Dis. 2010. PMID: 20525256 Free PMC article. Review.
The first neurological symptoms vary with age of onset: delay in developmental motor milestones (early infantile period), gait problems, falls, clumsiness, cataplexy, school problems (late infantile and juvenile period), and ataxia not unfrequently following initial psychi …
The first neurological symptoms vary with age of onset: delay in developmental motor milestones (early infantile period), gait problems, fal …
A dynamic developmental theory of attention-deficit/hyperactivity disorder (ADHD) predominantly hyperactive/impulsive and combined subtypes.
Sagvolden T, Johansen EB, Aase H, Russell VA. Sagvolden T, et al. Behav Brain Sci. 2005 Jun;28(3):397-419; discussion 419-68. doi: 10.1017/S0140525X05000075. Behav Brain Sci. 2005. PMID: 16209748 Review.
These impairments will give rise to apparent developmental delay, clumsiness, neurological "soft signs," and a "failure to inhibit" responses when quick reactions are required. Hypofunctioning dopamine branches represent the main individual predispositions in the present t …
These impairments will give rise to apparent developmental delay, clumsiness, neurological "soft signs," and a "failure to inhibit" r …
BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening.
Tangeraas T, Constante JR, Backe PH, Oyarzábal A, Neugebauer J, Weinhold N, Boemer F, Debray FG, Ozturk-Hism B, Evren G, Tuba EF, Ummuhan O, Footitt E, Davison J, Martinez C, Bueno C, Machado I, Rodríguez-Pombo P, Al-Sannaa N, De Los Santos M, López JM, Ozturkmen-Akay H, Karaca M, Tekin M, Pajares S, Ormazabal A, Stoway SD, Artuch R, Dixon M, Mørkrid L, García-Cazorla A. Tangeraas T, et al. Brain. 2023 Jul 3;146(7):3003-3013. doi: 10.1093/brain/awad010. Brain. 2023. PMID: 36729635
No microcephaly was observed at birth, but 17/20 developed microcephaly during follow-up. Regression was reported in six patients. Movement disorder was observed in 3/21 patients: hyperkinetic movements (1), truncal ataxia (1) and dystonia (2). ...
No microcephaly was observed at birth, but 17/20 developed microcephaly during follow-up. Regression was reported in six patients. Mo …
Cerebellum: From the identification of the cerebellar motor syndrome to the internal models.
Manto M, Mitoma H. Manto M, et al. Handb Clin Neurol. 2023;196:159-174. doi: 10.1016/B978-0-323-98817-9.00024-7. Handb Clin Neurol. 2023. PMID: 37620068 Review.
The leading hypothesis is that dysmetria results from errors in building or maintaining internal models, which are inherent to predictive behavior. Errors in prediction would lead to clumsiness and incoordination of limbs, oculomotor impairments, and aberrant …
The leading hypothesis is that dysmetria results from errors in building or maintaining internal models, which are inherent to predictive …
Cerebellar involvement in clumsiness and other developmental disorders.
Ivry RB. Ivry RB. Neural Plast. 2003;10(1-2):141-53. doi: 10.1155/NP.2003.141. Neural Plast. 2003. PMID: 14640315 Free PMC article. Review.
I review this literature, providing an analysis of different ways to consider the relation between cerebellar abnormalities and developmental disorders. Interestingly, although clumsiness is a problem of coordination, the contribution of cerebellar dysfunction to this deve …
I review this literature, providing an analysis of different ways to consider the relation between cerebellar abnormalities and developmenta …
Developmental coordination disorder: core sensori-motor deficits, neurobiology and etiology.
Gomez A, Sirigu A. Gomez A, et al. Neuropsychologia. 2015 Dec;79(Pt B):272-87. doi: 10.1016/j.neuropsychologia.2015.09.032. Epub 2015 Sep 28. Neuropsychologia. 2015. PMID: 26423663 Review.
High-level sensori-motor deficits are probably multifactorial in DCD and involve predictive coding deficits as well as weaknesses in perceptual and sensory integration. ...
High-level sensori-motor deficits are probably multifactorial in DCD and involve predictive coding deficits as well as weaknesses in …
Performance of Activities of daily living in people with multiple sclerosis.
Jansa J, Ferdinand S, Milo M, Løyning IG, Huilla T, Kallmayer L, Ilsbroukx S, Filló N, Raats J, Jakobson J, Kos D. Jansa J, et al. Mult Scler Relat Disord. 2022 Jan;57:103342. doi: 10.1016/j.msard.2021.103342. Epub 2021 Oct 21. Mult Scler Relat Disord. 2022. PMID: 35158429
Criterion referenced cut-off scores were established at 2.0 for motor skills and at 1.0 for process skills and both values above the cut-off score indicate competent (independent, safe, efficient and effortless) ADL performance. ...Overall, motor skills and process …
Criterion referenced cut-off scores were established at 2.0 for motor skills and at 1.0 for process skills and both values above the …
Childhood dyspraxia predicts adult-onset nonaffective-psychosis-spectrum disorder.
Schiffman J, Mittal V, Kline E, Mortensen EL, Michelsen N, Ekstrøm M, Millman ZB, Mednick SA, Sørensen HJ. Schiffman J, et al. Dev Psychopathol. 2015 Nov;27(4 Pt 1):1323-30. doi: 10.1017/S0954579414001436. Dev Psychopathol. 2015. PMID: 26439077
Several neurological variables have been investigated as premorbid biomarkers of vulnerability for schizophrenia and other related disorders. The current study examined whether childhood dyspraxia predicted later adult nonaffective-psychosis-spectrum disorders. From a stan …
Several neurological variables have been investigated as premorbid biomarkers of vulnerability for schizophrenia and other related disorders …
Cohen syndrome: essential features, natural history, and heterogeneity.
Kivitie-Kallio S, Norio R. Kivitie-Kallio S, et al. Am J Med Genet. 2001 Aug 1;102(2):125-35. doi: 10.1002/1096-8628(20010801)102:2<125::aid-ajmg1439>3.0.co;2-0. Am J Med Genet. 2001. PMID: 11477603 Review.
The diagnosis is based on the typical clinical picture: nonprogressive psychomotor retardation, motor clumsiness and microcephaly, typical facial features, childhood hypotonia and hyperextensibility of the joints, ophthalmologic findings of retinochoroidal dystrophy and my …
The diagnosis is based on the typical clinical picture: nonprogressive psychomotor retardation, motor clumsiness and microcephaly, ty …
Seesaw-Like Cervical Ossification of Posterior Longitudinal Ligament.
Zhang JN, Hao DJ. Zhang JN, et al. World Neurosurg. 2021 Jun;150:127-131. doi: 10.1016/j.wneu.2021.03.126. Epub 2021 Mar 31. World Neurosurg. 2021. PMID: 33812066
A 64-year-old man presented with a 10-month history of worsening clumsiness in the hands and impaired gait, and he occasionally had a feeling of an electric shock in the limbs when the neck was flexed. Physical examination revealed atrophy of the intrinsic hand muscles, ra …
A 64-year-old man presented with a 10-month history of worsening clumsiness in the hands and impaired gait, and he occasionally had a …
176 results