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Denise M Kay

Showing results (31-40 of 73) with videos related to

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Molecular Genetics and Metabolism|August 14, 2021
Prospective identification by neonatal screening of patients with guanidinoacetate methyltransferase deficiencyKim Hart, Andreas Rohrwasser, Heidi Wallis, et al.
Genetic Testing|October 6, 2006
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's diseaseDenise M Kay, Tom D Bird, Cyrus P Zabetian, et al.
Pediatric Pulmonology|March 1, 2024
Variability in evaluation and follow-up of newborns with CRMS/CFSPID in New York StateCatherine Kier, Denise M Kay, Elinor Langfelder-Schwind, et al.
Human Molecular Genetics|October 4, 2018
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosisJoão Fadista, Line Skotte, Frank Geller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 8, 2007
Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease riskKaren M Powers, Denise M Kay, Stewart A Factor, et al.
Annals of Neurology|May 22, 2007
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's diseaseCyrus P Zabetian, Carolyn M Hutter, Stewart A Factor, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2008
Genetic association between alpha-synuclein and idiopathic Parkinson's diseaseDenise M Kay, Stewart A Factor, Ali Samii, et al.
Pediatric Pulmonology|May 2, 2024
Genetic counseling access and service delivery in New York State is variable for parents of infants with complex CFTR genotypes conferring uncertain phenotypesDenise M Kay, Hossein Sadeghi, Catherine Kier, et al.
European Journal of Neurology|December 21, 2007
Lack of evidence for an association between UCHL1 S18Y and Parkinson's diseaseCarolyn M Hutter, Ali Samii, Stewart A Factor, et al.
European Journal of Medical Genetics|November 28, 2017
Rare copy number variants identified in prune belly syndromeNansi S Boghossian, Robert J Sicko, Andreas Giannakou, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Molecular Genetics and Metabolism|August 14, 2021
Prospective identification by neonatal screening of patients with guanidinoacetate methyltransferase deficiencyKim Hart, Andreas Rohrwasser, Heidi Wallis, et al.
Genetic Testing|October 6, 2006
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's diseaseDenise M Kay, Tom D Bird, Cyrus P Zabetian, et al.
Pediatric Pulmonology|March 1, 2024
Variability in evaluation and follow-up of newborns with CRMS/CFSPID in New York StateCatherine Kier, Denise M Kay, Elinor Langfelder-Schwind, et al.
Human Molecular Genetics|October 4, 2018
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosisJoão Fadista, Line Skotte, Frank Geller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 8, 2007
Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease riskKaren M Powers, Denise M Kay, Stewart A Factor, et al.
Annals of Neurology|May 22, 2007
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's diseaseCyrus P Zabetian, Carolyn M Hutter, Stewart A Factor, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2008
Genetic association between alpha-synuclein and idiopathic Parkinson's diseaseDenise M Kay, Stewart A Factor, Ali Samii, et al.
Pediatric Pulmonology|May 2, 2024
Genetic counseling access and service delivery in New York State is variable for parents of infants with complex CFTR genotypes conferring uncertain phenotypesDenise M Kay, Hossein Sadeghi, Catherine Kier, et al.
European Journal of Neurology|December 21, 2007
Lack of evidence for an association between UCHL1 S18Y and Parkinson's diseaseCarolyn M Hutter, Ali Samii, Stewart A Factor, et al.
European Journal of Medical Genetics|November 28, 2017
Rare copy number variants identified in prune belly syndromeNansi S Boghossian, Robert J Sicko, Andreas Giannakou, et al.
Pageof 8