Header Logo

Search Result Details

Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
Berry-Kravis, Elizabeth
One or more keywords matched the following items that are connected to Berry-Kravis, Elizabeth
Item TypeName
Concept Cell Death
Concept Sudden Infant Death
Concept Death, Sudden
Academic Article Viral delivery of glial cell line-derived neurotrophic factor improves behavior and protects striatal neurons in a mouse model of Huntington's disease.
Academic Article Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.
Academic Article Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.
Academic Article Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death.
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 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 Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulation.
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: review of implicated genetic factors.
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 Fragile X Gray Zone Alleles Are Associated With Signs of Parkinsonism and Earlier Death.
Search Criteria
  • Death