Detalhe da pesquisa
1.
Comparison of Polysomnography, Single-Channel Electroencephalogram, Fitbit, and Sleep Logs in Patients With Psychiatric Disorders: Cross-Sectional Study.
J Med Internet Res
; 25: e51336, 2023 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38090797
2.
Prevalence of obstructive sleep apnea as assessed by polysomnography in psychiatric patients with sleep-related problems.
Sleep Breath
; 26(4): 1983-1991, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35029795
3.
SMOC1 is essential for ocular and limb development in humans and mice.
Am J Hum Genet
; 88(1): 30-41, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21194678
4.
Assessing the Real-World, Long-Term Impact of Lemborexant on Sleep Quality in a Home-Based Clinical Study.
Nat Sci Sleep
; 16: 291-303, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38524766
5.
Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delay.
Am J Hum Genet
; 86(6): 881-91, 2010 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20493457
6.
Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies.
Am J Med Genet A
; 161A(7): 1543-6, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23703728
7.
LPS and its relationship with subjective-objective discrepancies of sleep onset latency in patients with psychiatric disorders.
Sci Rep
; 13(1): 22637, 2023 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38114534
8.
A Study of Factors Causing Sleep State Misperception in Patients with Depression.
Nat Sci Sleep
; 14: 1273-1283, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35873712
9.
De novo 5q14.3 translocation 121.5-kb upstream of MEF2C in a patient with severe intellectual disability and early-onset epileptic encephalopathy.
Am J Med Genet A
; 155A(11): 2879-84, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21990267
10.
FLUID study: study protocol for an open-label, single-centre pilot study to investigate the efFect of Lemborexant on sleep management in Japanese sUbjects aged 50 years and older with Insomnia Disorder.
BMJ Open
; 11(11): e054885, 2021 11 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34836909
11.
STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.
Epilepsia
; 51(12): 2397-405, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20887364
12.
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.
Nat Genet
; 44(4): 376-8, 2012 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22426308
13.
De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.
Nat Genet
; 40(6): 782-8, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18469812