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Elizabeth M Berry-Kravis

Showing results (1-10 of 86) with videos related to

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American Journal of Respiratory and Critical Care Medicine|April 24, 2004
Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan diseaseDebra E Weese-Mayer, Elizabeth M Berry-Kravis
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 29, 2011
Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyondChristina Gross, Elizabeth M Berry-Kravis, Gary J Bassell
Journal of Neuroscience Methods|February 19, 2022
Independent evaluation of the harvard automated processing pipeline for Electroencephalography 1.0 using multi-site EEG data from children with Fragile X SyndromeEmma Auger, Elizabeth M Berry-Kravis, Lauren E Ethridge
American Journal of Respiratory and Critical Care Medicine|December 24, 2004
Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHSDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 20, 2015
Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and BackChristina Gross, Anne Hoffmann, Gary J Bassell, et al.
Respiratory Physiology & Neurobiology|August 2, 2005
In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndromeDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Mary L Marazita
Journal of Alzheimer'S Disease & Parkinsonism|March 6, 2013
Effect of Anticoagulants on Amyloid β-Protein Precursor and Amyloid Beta Levels in PlasmaCara J Westmark, Crystal M Hervey, Elizabeth M Berry-Kravis, et al.
American Journal of Respiratory and Critical Care Medicine|August 5, 2006
Congenital central hypoventilation syndrome: PHOX2B mutations and phenotypeElizabeth M Berry-Kravis, Lili Zhou, Casey M Rand, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2026
Interaction of FXTAS Family History and College Degree Attainment Predicts Trajectories of Cognitive and Motor Symptoms in FMR1 Premutation Carrier WomenJinkuk Hong, Leann Smith DaWalt, Jessica Klusek, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 6, 2008
HTR2A variation and sudden infant death syndrome: a case-control analysisCasey M Rand, Elizabeth M Berry-Kravis, Wenqing Fan, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
American Journal of Respiratory and Critical Care Medicine|April 24, 2004
Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan diseaseDebra E Weese-Mayer, Elizabeth M Berry-Kravis
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|July 29, 2011
Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyondChristina Gross, Elizabeth M Berry-Kravis, Gary J Bassell
Journal of Neuroscience Methods|February 19, 2022
Independent evaluation of the harvard automated processing pipeline for Electroencephalography 1.0 using multi-site EEG data from children with Fragile X SyndromeEmma Auger, Elizabeth M Berry-Kravis, Lauren E Ethridge
American Journal of Respiratory and Critical Care Medicine|December 24, 2004
Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHSDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 20, 2015
Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and BackChristina Gross, Anne Hoffmann, Gary J Bassell, et al.
Respiratory Physiology & Neurobiology|August 2, 2005
In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndromeDebra E Weese-Mayer, Elizabeth M Berry-Kravis, Mary L Marazita
Journal of Alzheimer'S Disease & Parkinsonism|March 6, 2013
Effect of Anticoagulants on Amyloid β-Protein Precursor and Amyloid Beta Levels in PlasmaCara J Westmark, Crystal M Hervey, Elizabeth M Berry-Kravis, et al.
American Journal of Respiratory and Critical Care Medicine|August 5, 2006
Congenital central hypoventilation syndrome: PHOX2B mutations and phenotypeElizabeth M Berry-Kravis, Lili Zhou, Casey M Rand, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2026
Interaction of FXTAS Family History and College Degree Attainment Predicts Trajectories of Cognitive and Motor Symptoms in FMR1 Premutation Carrier WomenJinkuk Hong, Leann Smith DaWalt, Jessica Klusek, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 6, 2008
HTR2A variation and sudden infant death syndrome: a case-control analysisCasey M Rand, Elizabeth M Berry-Kravis, Wenqing Fan, et al.
Pageof 9