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Elizabeth M Berry-Kravis

Showing results (11-20 of 86) with videos related to

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Respiratory Physiology & Neurobiology|June 27, 2008
Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulationDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Isabella Ceccherini, et al.
Frontiers in Psychiatry|August 30, 2021
Is <i>FMR1</i> CGG Repeat Number Polymorphism Associated With Phenotypic Variation in the General Population? Report From a Cohort of 5,499 AdultsJinkuk Hong, Leann DaWalt, Mei Wang Baker, et al.
American Journal of Medical Genetics. Part A|March 7, 2007
Sudden Infant Death Syndrome: review of implicated genetic factorsDebra E Weese-Mayer, Michael J Ackerman, Mary L Marazita, et al.
American Journal on Intellectual and Developmental Disabilities|April 27, 2023
Health Effects of Sleep Quality in Premutation Carrier Mothers of Individuals With Fragile X SyndromeRobert S Dembo, Jinkuk Hong, Leann Smith DaWalt, et al.
Frontiers in Cellular Neuroscience|June 12, 2013
Developing BACE-1 inhibitors for FXSCara J Westmark, Elizabeth M Berry-Kravis, Chrysanthy Ikonomidou, et al.
Indian Journal of Pediatrics|July 26, 2012
Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?Nilay Nirupam, Rajni Sharma, Viswas Chhapola, et al.
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.
SSM - Population Health|October 14, 2022
The effect of college degree attainment on neurodegenerative symptoms in genetically at-risk womenJinkuk Hong, Robert S Dembo, Leann Smith DaWalt, et al.
Pediatric Pulmonology|November 29, 2007
Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden deathJerome O Gronli, Barbara A Santucci, Sue E Leurgans, et al.
Pediatrics|August 3, 2011
Monozygotic twins discordant for ROHHAD phenotypePallavi P Patwari, Casey M Rand, Elizabeth M Berry-Kravis, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
Respiratory Physiology & Neurobiology|June 27, 2008
Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulationDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Isabella Ceccherini, et al.
Frontiers in Psychiatry|August 30, 2021
Is <i>FMR1</i> CGG Repeat Number Polymorphism Associated With Phenotypic Variation in the General Population? Report From a Cohort of 5,499 AdultsJinkuk Hong, Leann DaWalt, Mei Wang Baker, et al.
American Journal of Medical Genetics. Part A|March 7, 2007
Sudden Infant Death Syndrome: review of implicated genetic factorsDebra E Weese-Mayer, Michael J Ackerman, Mary L Marazita, et al.
American Journal on Intellectual and Developmental Disabilities|April 27, 2023
Health Effects of Sleep Quality in Premutation Carrier Mothers of Individuals With Fragile X SyndromeRobert S Dembo, Jinkuk Hong, Leann Smith DaWalt, et al.
Frontiers in Cellular Neuroscience|June 12, 2013
Developing BACE-1 inhibitors for FXSCara J Westmark, Elizabeth M Berry-Kravis, Chrysanthy Ikonomidou, et al.
Indian Journal of Pediatrics|July 26, 2012
Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?Nilay Nirupam, Rajni Sharma, Viswas Chhapola, et al.
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.
SSM - Population Health|October 14, 2022
The effect of college degree attainment on neurodegenerative symptoms in genetically at-risk womenJinkuk Hong, Robert S Dembo, Leann Smith DaWalt, et al.
Pediatric Pulmonology|November 29, 2007
Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden deathJerome O Gronli, Barbara A Santucci, Sue E Leurgans, et al.
Pediatrics|August 3, 2011
Monozygotic twins discordant for ROHHAD phenotypePallavi P Patwari, Casey M Rand, Elizabeth M Berry-Kravis, et al.
Pageof 9