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Search Results to Elizabeth Berry-Kravis

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

Item TypeName
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.

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