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The relationships between improvements in daytime sleepiness, fatigue and depression and psychomotor vigilance task testing with CPAP use in patients with obstructive sleep apnea

Autor: Hinesh Upadhyay, Vincent A. DeBari, Shaista Akhtar, Omar Akel, Sue X. Ming, Divya Gupta, Sudhansu Chokroverty, Peter G. Polos, Sushanth Bhat, Anna McIntyre

Publikováno v: Sleep medicine. 49

Objective The purpose of this study was to determine if the subjective improvements in daytime sleepiness, fatigue and depression experienced by patients with obstructive sleep apnea (OSA) with continuous positive airway pressure (CPAP) therapy predi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b96ebc030cda1fd56530ecf2f0df891
https://pubmed.ncbi.nlm.nih.gov/30093261

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New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

Autor: William G. Johnson, John R. Spychala, Sue X. Ming, Edward S. Stenroos, Steven Buyske, Sansnee Chatkupt

Publikováno v: American Journal of Medical Genetics. :339-345

Up to 72% of spina bifida cystica (SB) is preventable by maternal periconceptual folic acid supplementation. The C677T allele of the methylenetetrahydrofolate reductase (MTHFR) gene and some other functional polymorphisms are risk factors for SB in s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1188000733f2a93c680dd27d9650f6d0
https://doi.org/10.1002/ajmg.a.20505

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Brief report: the impact of subcortical band heterotopia and associated complications on the neuropsychological functioning of a 13-year-old child

Autor: James M. Hill, Sue X. Ming, Beata S. Beaudoin

Publikováno v: Journal of autism and developmental disorders. 37(5)

Motor impairment in children with Asperger syndrome (AS) or high functioning autism (HFA) has been reported previously. This study presents results of a quantitative assessment of neuromotor skills in 14-22 year old HFA/AS. Sixteen HFA/AS and 16 IQ-m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e89818413b6953c8243c1a0f854ab9b
https://pubmed.ncbi.nlm.nih.gov/17160462

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Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism

Autor: Tanishia A. Williams, Marivic F Factura, Audrey E. Mars, Chitra Reddy, Edward S. Stenroos, George H. Lambert, Sue X. Ming, Rong Wang, William G. Johnson, Steven Buyske, Madhura Sreenath

Publikováno v: BMC Genetics
BMC Genetics, Vol 7, Iss 1, p 8 (2006)

Background Certain loci on the human genome, such as glutathione S-transferase M1 (GSTM1), do not permit heterozygotes to be reliably determined by commonly used methods. Association of such a locus with a disease is therefore generally tested with a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::570381bc0c59ce325960463e8c20733f
https://doi.org/10.1186/1471-2156-7-8

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