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Casey M Rand

Showing results (11-20 of 57) with videos related to

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Pediatric Research|June 29, 2007
Sudden infant death syndrome: rare mutation in the serotonin system FEV geneCasey M Rand, Elizabeth M Berry-Kravis, Lili Zhou, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|June 16, 2023
A narrative review of the mechanisms and consequences of intermittent hypoxia and the role of advanced analytic techniques in pediatric autonomic disordersJan-Marino Ramirez, Michael S Carroll, Nicholas Burgraff, et al.
Human Mutation|March 11, 2026
Recognition of a Critical Functional Domain and Improved <i>PHOX2B</i> Missense Variant Interpretation by Utilization of In Silico Prediction ToolsAndy Drackley, Andrew D Skol, Casey M Rand, et al.
Pediatric Pulmonology|January 13, 2018
Congenital central hypoventilation syndrome: Broader cognitive deficits revealed by parent controlsFrank A Zelko, Tracey M Stewart, Cindy D Brogadir, et al.
Annals of the American Thoracic Society|February 21, 2026
Heart Rate Variability: Longitudinal Cardioautonomic Physiomarker in Congenital Central Hypoventilation SyndromeJoely R Gendler, Amy Zhou, Casey M Rand, et al.
Respiratory Physiology & Neurobiology|July 6, 2010
Congenital central hypoventilation syndrome and the PHOX2B gene: a model of respiratory and autonomic dysregulationPallavi P Patwari, Michael S Carroll, Casey M Rand, et al.
Pediatric Pulmonology|March 28, 2025
Reliability of Composite Autonomic Symptom Score (COMPASS)-31 in Congenital Central Hypoventilation SyndromeBenjamin Dudoignon, Plamen Bokov, Fatima Benterki, et al.
Pediatrics|August 3, 2011
Monozygotic twins discordant for ROHHAD phenotypePallavi P Patwari, Casey M Rand, Elizabeth M Berry-Kravis, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 6, 2010
Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriersLawrence J Jennings, Min Yu, Lili Zhou, et al.
American Journal of Medical Genetics. Part A|February 21, 2008
Genetic variation in the HTR1A gene and sudden infant death syndromeMegan E Morley, Casey M Rand, Elizabeth M Berry-Kravis, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Pediatric Research|June 29, 2007
Sudden infant death syndrome: rare mutation in the serotonin system FEV geneCasey M Rand, Elizabeth M Berry-Kravis, Lili Zhou, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|June 16, 2023
A narrative review of the mechanisms and consequences of intermittent hypoxia and the role of advanced analytic techniques in pediatric autonomic disordersJan-Marino Ramirez, Michael S Carroll, Nicholas Burgraff, et al.
Human Mutation|March 11, 2026
Recognition of a Critical Functional Domain and Improved <i>PHOX2B</i> Missense Variant Interpretation by Utilization of In Silico Prediction ToolsAndy Drackley, Andrew D Skol, Casey M Rand, et al.
Pediatric Pulmonology|January 13, 2018
Congenital central hypoventilation syndrome: Broader cognitive deficits revealed by parent controlsFrank A Zelko, Tracey M Stewart, Cindy D Brogadir, et al.
Annals of the American Thoracic Society|February 21, 2026
Heart Rate Variability: Longitudinal Cardioautonomic Physiomarker in Congenital Central Hypoventilation SyndromeJoely R Gendler, Amy Zhou, Casey M Rand, et al.
Respiratory Physiology & Neurobiology|July 6, 2010
Congenital central hypoventilation syndrome and the PHOX2B gene: a model of respiratory and autonomic dysregulationPallavi P Patwari, Michael S Carroll, Casey M Rand, et al.
Pediatric Pulmonology|March 28, 2025
Reliability of Composite Autonomic Symptom Score (COMPASS)-31 in Congenital Central Hypoventilation SyndromeBenjamin Dudoignon, Plamen Bokov, Fatima Benterki, et al.
Pediatrics|August 3, 2011
Monozygotic twins discordant for ROHHAD phenotypePallavi P Patwari, Casey M Rand, Elizabeth M Berry-Kravis, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 6, 2010
Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriersLawrence J Jennings, Min Yu, Lili Zhou, et al.
American Journal of Medical Genetics. Part A|February 21, 2008
Genetic variation in the HTR1A gene and sudden infant death syndromeMegan E Morley, Casey M Rand, Elizabeth M Berry-Kravis, et al.
Pageof 6