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Andrea Gropman

Showing results (51-60 of 86) with videos related to

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Archives of Neurology|December 17, 2009
Subdural fluid collections in patients with infantile neuronal ceroid lipofuscinosisSondra W Levin, Eva H Baker, Andrea Gropman, et al.
Clinical Epigenetics|July 2, 2021
DNA methylation and behavioral dysfunction in males with 47,XXY and 49,XXXXY: a pilot studyRichard S Lee, Sophia Q Song, Henri M Garrison-Desany, et al.
Pediatric Neurology|August 9, 2024
Unraveling the Link: Seizure Characteristics and Ammonia Levels in Urea Cycle Disorder During Hyperammonemic CrisesMongkol Chanvanichtrakool, John M Schreiber, Wei-Liang Chen, et al.
Epilepsy & Behavior : E&B|February 7, 2018
Prospective longitudinal overnight video-EEG evaluation in Phelan-McDermid SyndromeOmar I Khan, Xiangping Zhou, Jill Leon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndromeChristopher A Wassif, Lisa Kratz, Susan E Sparks, et al.
JCI Insight|September 6, 2019
Hepatic arginase deficiency fosters dysmyelination during postnatal CNS developmentXiao-Bo Liu, Jillian R Haney, Gloria Cantero, et al.
Frontiers in Genetics|January 31, 2022
Case Report: Infant With Congenital Adrenal Hyperplasia and 47,XXYSophia Q Song, Andrea Gropman, Robert W Benjamin, et al.
Diseases (Basel, Switzerland)|September 22, 2017
Role of Diffusion Tensor Imaging in Prognostication and Treatment Monitoring in Niemann-Pick Disease Type C1Meghann W Lau, Ryan W Lee, Robin Miyamoto, et al.
Anesthesia and Analgesia|July 18, 2009
Children with infantile neuronal ceroid lipofuscinosis have an increased risk of hypothermia and bradycardia during anesthesiaNing Miao, Sondra W Levin, Eva H Baker, et al.
American Journal of Human Genetics|May 5, 2023
The functional impact of 1,570 individual amino acid substitutions in human OTCRussell S Lo, Gareth A Cromie, Michelle Tang, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Archives of Neurology|December 17, 2009
Subdural fluid collections in patients with infantile neuronal ceroid lipofuscinosisSondra W Levin, Eva H Baker, Andrea Gropman, et al.
Clinical Epigenetics|July 2, 2021
DNA methylation and behavioral dysfunction in males with 47,XXY and 49,XXXXY: a pilot studyRichard S Lee, Sophia Q Song, Henri M Garrison-Desany, et al.
Pediatric Neurology|August 9, 2024
Unraveling the Link: Seizure Characteristics and Ammonia Levels in Urea Cycle Disorder During Hyperammonemic CrisesMongkol Chanvanichtrakool, John M Schreiber, Wei-Liang Chen, et al.
Epilepsy & Behavior : E&B|February 7, 2018
Prospective longitudinal overnight video-EEG evaluation in Phelan-McDermid SyndromeOmar I Khan, Xiangping Zhou, Jill Leon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 12, 2016
A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndromeChristopher A Wassif, Lisa Kratz, Susan E Sparks, et al.
JCI Insight|September 6, 2019
Hepatic arginase deficiency fosters dysmyelination during postnatal CNS developmentXiao-Bo Liu, Jillian R Haney, Gloria Cantero, et al.
Frontiers in Genetics|January 31, 2022
Case Report: Infant With Congenital Adrenal Hyperplasia and 47,XXYSophia Q Song, Andrea Gropman, Robert W Benjamin, et al.
Diseases (Basel, Switzerland)|September 22, 2017
Role of Diffusion Tensor Imaging in Prognostication and Treatment Monitoring in Niemann-Pick Disease Type C1Meghann W Lau, Ryan W Lee, Robin Miyamoto, et al.
Anesthesia and Analgesia|July 18, 2009
Children with infantile neuronal ceroid lipofuscinosis have an increased risk of hypothermia and bradycardia during anesthesiaNing Miao, Sondra W Levin, Eva H Baker, et al.
American Journal of Human Genetics|May 5, 2023
The functional impact of 1,570 individual amino acid substitutions in human OTCRussell S Lo, Gareth A Cromie, Michelle Tang, et al.
Pageof 9