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

Year Number of Results
1968 2
1969 1
1970 1
1973 2
1974 4
1975 7
1976 5
1977 7
1978 9
1979 9
1980 5
1981 7
1982 10
1983 21
1984 23
1985 16
1986 15
1987 16
1988 18
1989 23
1990 19
1991 35
1992 29
1993 34
1994 41
1995 57
1996 36
1997 25
1998 43
1999 44
2000 52
2001 53
2002 52
2003 74
2004 65
2005 73
2006 74
2007 94
2008 112
2009 102
2010 94
2011 91
2012 99
2013 123
2014 112
2015 82
2016 76
2017 75
2018 89
2019 82
2020 71
2021 60
2022 61
2023 49
2024 19

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2,206 results

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Quoted phrase not found in phrase index: "Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome"
Page 1
The trisomy 18 syndrome.
Cereda A, Carey JC. Cereda A, et al. Orphanet J Rare Dis. 2012 Oct 23;7:81. doi: 10.1186/1750-1172-7-81. Orphanet J Rare Dis. 2012. PMID: 23088440 Free PMC article. Review.
The trisomy 18 syndrome, also known as Edwards syndrome, is a common chromosomal disorder due to the presence of an extra chromosome 18, either full, mosaic trisomy, or partial trisomy 18q. ...Currently most cases of trisomy 18 are prenatally diagnosed, based on scr …
The trisomy 18 syndrome, also known as Edwards syndrome, is a common chromosomal disorder due to the presence of an extra chro …
Benzodiazepines Remain Important Therapeutic Options in Psychiatric Practice.
Dubovsky SL, Marshall D. Dubovsky SL, et al. Psychother Psychosom. 2022;91(5):307-334. doi: 10.1159/000524400. Epub 2022 May 3. Psychother Psychosom. 2022. PMID: 35504267 Free article. Review.
Data presented in this article support the use of these medications as treatments of choice for acute situational anxiety, chronic anxiety disorders, insomnia, alcohol withdrawal syndromes, and catatonia. They may also be useful adjuncts in the treatment of anxious depress …
Data presented in this article support the use of these medications as treatments of choice for acute situational anxiety, chronic anxiety d …
Music-based therapeutic interventions for people with dementia.
van der Steen JT, Smaling HJ, van der Wouden JC, Bruinsma MS, Scholten RJ, Vink AC. van der Steen JT, et al. Cochrane Database Syst Rev. 2018 Jul 23;7(7):CD003477. doi: 10.1002/14651858.CD003477.pub4. Cochrane Database Syst Rev. 2018. PMID: 30033623 Free PMC article. Review.
BACKGROUND: Dementia is a clinical syndrome with a number of different causes which is characterised by deterioration in cognitive, behavioural, social and emotional functions. Pharmacological interventions are available but have limited effect to treat many of the synd …
BACKGROUND: Dementia is a clinical syndrome with a number of different causes which is characterised by deterioration in cognitive, b …
The psychopharmacology of catatonia, neuroleptic malignant syndrome, akathisia, tardive dyskinesia, and dystonia.
Sienaert P, van Harten P, Rhebergen D. Sienaert P, et al. Handb Clin Neurol. 2019;165:415-428. doi: 10.1016/B978-0-444-64012-3.00025-3. Handb Clin Neurol. 2019. PMID: 31727227 Review.
Although highly prevalent, motor syndromes in psychiatry and motor side effects of psychopharmacologic agents remain understudied. Catatonia is a syndrome with specific motor abnormalities that can be seen in the context of a variety of psychiatric and somatic condi …
Although highly prevalent, motor syndromes in psychiatry and motor side effects of psychopharmacologic agents remain understudied. Ca …
Music-based therapeutic interventions for people with dementia.
van der Steen JT, van Soest-Poortvliet MC, van der Wouden JC, Bruinsma MS, Scholten RJ, Vink AC. van der Steen JT, et al. Cochrane Database Syst Rev. 2017 May 2;5(5):CD003477. doi: 10.1002/14651858.CD003477.pub3. Cochrane Database Syst Rev. 2017. PMID: 28462986 Free PMC article. Updated. Review.
BACKGROUND: Dementia is a clinical syndrome with a number of different causes which is characterised by deterioration in cognitive, behavioural, social and emotional functions. Pharmacological interventions are available but have limited effect to treat many of the synd …
BACKGROUND: Dementia is a clinical syndrome with a number of different causes which is characterised by deterioration in cognitive, b …
Mowat-Wilson syndrome.
Garavelli L, Mainardi PC. Garavelli L, et al. Orphanet J Rare Dis. 2007 Oct 24;2:42. doi: 10.1186/1750-1172-2-42. Orphanet J Rare Dis. 2007. PMID: 17958891 Free PMC article. Review.
Studies of genotype-phenotype analysis show that facial gestalt and delayed psychomotor development are constant clinical features, while the frequent and severe congenital malformations are variable. ...Congenital malformations and seizures require precocious clinical inv …
Studies of genotype-phenotype analysis show that facial gestalt and delayed psychomotor development are constant clinical features, w …
Chronic Brain Failure.
Wolak JP. Wolak JP. Emerg Med Clin North Am. 2021 May;39(2):307-322. doi: 10.1016/j.emc.2021.01.008. Emerg Med Clin North Am. 2021. PMID: 33863461 Review.
Chronic brain failure, also known as dementia or major neurocognitive disorder, is a syndrome of progressive functional decline characterized by both cognitive and neuropsychiatric symptoms. It can be conceptualized like other organ failure syndromes and its impact …
Chronic brain failure, also known as dementia or major neurocognitive disorder, is a syndrome of progressive functional decline chara …
Serine-deficiency syndromes.
de Koning TJ, Klomp LW. de Koning TJ, et al. Curr Opin Neurol. 2004 Apr;17(2):197-204. doi: 10.1097/00019052-200404000-00019. Curr Opin Neurol. 2004. PMID: 15021249 Review.
Recent findings concerning these roles of L-serine-derived phospholipids and neurotransmitters are presented. SUMMARY: Congenital microcephaly, seizures and severe psychomotor retardation are symptoms of serine deficiency and can be treated with supplementation of L-serine …
Recent findings concerning these roles of L-serine-derived phospholipids and neurotransmitters are presented. SUMMARY: Congenital microcepha …
Alstrom syndrome.
Marshall JD, Beck S, Maffei P, Naggert JK. Marshall JD, et al. Eur J Hum Genet. 2007 Dec;15(12):1193-202. doi: 10.1038/sj.ejhg.5201933. Epub 2007 Oct 17. Eur J Hum Genet. 2007. PMID: 17940554
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently unknown molecular function. ...Most patients demonstrate normal intelligence, although some reports indicate delayed psychomotor and i …
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently u …
Movement disorder and sensorimotor abnormalities in schizophrenia and other psychoses - European consensus on assessment and perspectives.
Walther S, van Harten PN, Waddington JL, Cuesta MJ, Peralta V, Dupin L, Foucher JR, Sambataro F, Morrens M, Kubera KM, Pieters LE, Stegmayer K, Strik W, Wolf RC, Hirjak D. Walther S, et al. Eur Neuropsychopharmacol. 2020 Sep;38:25-39. doi: 10.1016/j.euroneuro.2020.07.003. Epub 2020 Jul 23. Eur Neuropsychopharmacol. 2020. PMID: 32713718 Review.
Over the last three decades, movement disorder as well as sensorimotor and psychomotor functioning in schizophrenia (SZ) and other psychoses has gained greater scientific and clinical relevance as an intrinsic component of the disease process of psychotic illness; this ext …
Over the last three decades, movement disorder as well as sensorimotor and psychomotor functioning in schizophrenia (SZ) and other ps …
2,206 results