Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Casey M Rand

Showing results (21-30 of 57) with videos related to

Pageof 6
Sort By:
American Journal of Medical Genetics. Part A|June 10, 2006
Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndromeCasey M Rand, Debra E Weese-Mayer, Brion S Maher, et al.
Frontiers in Pediatrics|May 26, 2023
Analysis and comparisons of gene expression changes in patient- derived neurons from ROHHAD, CCHS, and PWSA Kaitlyn Victor, Tayler Hedgecock, Martin Donaldson, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS)Casey M Rand, Min Yu, Lawrence J Jennings, et al.
Pediatric Pulmonology|August 11, 2011
Variable human phenotype associated with novel deletions of the PHOX2B geneLawrence J Jennings, Min Yu, Casey M Rand, et al.
Pediatric Pulmonology|May 16, 2022
Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®Remi Z Welbel, Casey M Rand, Amy Zhou, et al.
Pediatric Pulmonology|May 8, 2009
Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicineDebra E Weese-Mayer, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A|January 24, 2019
Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family membersYakov Sivan, Amy Zhou, Lawrence J Jennings, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 19, 2008
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B geneGabriela M Repetto, Raul J Corrales, Selim G Abara, et al.
American Journal of Medical Genetics. Part A|July 11, 2006
Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B geneCasey M Rand, Debra E Weese-Mayer, Lili Zhou, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|October 26, 2022
Neurocognition as a biomarker in the rare autonomic disorders of CCHS and ROHHADFrank A Zelko, Remi Z Welbel, Casey M Rand, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|June 10, 2006
Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndromeCasey M Rand, Debra E Weese-Mayer, Brion S Maher, et al.
Frontiers in Pediatrics|May 26, 2023
Analysis and comparisons of gene expression changes in patient- derived neurons from ROHHAD, CCHS, and PWSA Kaitlyn Victor, Tayler Hedgecock, Martin Donaldson, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS)Casey M Rand, Min Yu, Lawrence J Jennings, et al.
Pediatric Pulmonology|August 11, 2011
Variable human phenotype associated with novel deletions of the PHOX2B geneLawrence J Jennings, Min Yu, Casey M Rand, et al.
Pediatric Pulmonology|May 16, 2022
Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®Remi Z Welbel, Casey M Rand, Amy Zhou, et al.
Pediatric Pulmonology|May 8, 2009
Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicineDebra E Weese-Mayer, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A|January 24, 2019
Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family membersYakov Sivan, Amy Zhou, Lawrence J Jennings, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 19, 2008
Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B geneGabriela M Repetto, Raul J Corrales, Selim G Abara, et al.
American Journal of Medical Genetics. Part A|July 11, 2006
Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B geneCasey M Rand, Debra E Weese-Mayer, Lili Zhou, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|October 26, 2022
Neurocognition as a biomarker in the rare autonomic disorders of CCHS and ROHHADFrank A Zelko, Remi Z Welbel, Casey M Rand, et al.
Pageof 6