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Berry-Kravis, Elizabeth

One or more keywords matched the following items that are connected to Berry-Kravis, Elizabeth

Item Type	Name
Concept	Case-Control Studies
Academic Article	Amyloid mediates the association of apolipoprotein E e4 allele to cognitive function in older people.
Academic Article	Genetic polymorphisms in Parkinson disease subjects with and without hallucinations: an analysis of the cholecystokinin system.
Academic Article	Racial differences may influence the role of cholecystokinin polymorphisms in Parkinson's disease hallucinations.
Academic Article	Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.
Academic Article	Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.
Academic Article	Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.
Academic Article	Genetic variation analysis in parkinson disease patients with and without hallucinations: case-control study.
Academic Article	Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.
Academic Article	Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome.
Academic Article	Autonomic regulation in fragile X syndrome.
Academic Article	Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome.
Academic Article	Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).
Academic Article	HTR2A variation and sudden infant death syndrome: a case-control analysis.
Academic Article	Genetic variation in the HTR1A gene and sudden infant death syndrome.
Academic Article	Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.
Academic Article	Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.
Academic Article	Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome.
Academic Article	3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis.
Academic Article	Neurological and endocrine phenotypes of fragile X carrier women.
Academic Article	Prepulse inhibition in fragile X syndrome: feasibility, reliability, and implications for treatment.
Academic Article	Diagnosis of niemann-pick C1 by measurement of bile acid biomarkers in archived newborn dried blood spots.
Academic Article	Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation.
Academic Article	Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation.
Academic Article	Soy-Based Infant Formula is Associated with an Increased Prevalence of Comorbidities in Fragile X Syndrome.
Academic Article	Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation.

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Case Control Studies