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Seizure|April 9, 2011
Successful treatment of childhood prolonged refractory status epilepticus with lacosamideYael Shiloh-Malawsky, Zheng Fan, Robert Greenwood, et al.
International Journal of Computer Assisted Radiology and Surgery|January 10, 2013
A computerized MRI biomarker quantification scheme for a canine model of Duchenne muscular dystrophyJiahui Wang, Zheng Fan, Krista Vandenborne, et al.
Frontiers in Cellular Neuroscience|October 16, 2023
A homozygous missense variant in the YG box domain in an individual with severe spinal muscular atrophy: a case report and variant characterizationLeping Li, Lalith Perera, Sonia A Varghese, et al.
Epilepsia|August 18, 2021
Add-on cannabidiol in patients with Dravet syndrome: Results of a long-term open-label extension trialIngrid E Scheffer, Jonathan J Halford, Ian Miller, et al.
Neuromuscular Disorders : NMD|December 4, 2013
Characteristics of magnetic resonance imaging biomarkers in a natural history study of golden retriever muscular dystrophyZheng Fan, Jiahui Wang, Mihye Ahn, et al.
The Journal of Pediatric Pharmacology and Therapeutics : JPPT : the Official Journal of PPAG|December 14, 2023
Pharmacokinetics and Proposed Dosing of Levetiracetam in Children With ObesityKanecia O Zimmerman, Huali Wu, Anil Maharaj, et al.
American Journal of Medical Genetics. Part A|September 11, 2025
Long-Read Sequencing of a Neurodevelopmental Disorder Patient Reveals Complex Rearrangement Involving the ARID1B GeneTam P Sneddon, Scott A Melville, Mai Xiong, et al.
Neurology. Genetics|February 9, 2018
Diagnostic utility of exome sequencing in the evaluation of neuromuscular disordersGloria T Haskell, Michael C Adams, Zheng Fan, et al.
Human Molecular Genetics|July 15, 2026
SPEN deficiency contributes to the development of orofacial clefts in humans and miceBum Jun Kim, Andrés Hernández-García, David L Curtis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
New genotype-phenotype correlations and management recommendations for individuals with RERE variantsDavid Curtis, Xiaonan Zhao, Nichole M Owen, et al.
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