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Human Immunology|May 16, 2006
Transcriptional control of activation-induced cytidine deaminase and error-prone DNA polymerases is functionally mature in the B cells of infants at birthAmber L Bowen, Cuixia Tian, Bonnie J LaFleur, et al.
Molecular Genetics & Genomic Medicine|November 25, 2022
Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49-51 deletion phenotypeElizabeth A Ulm, Chinmayee B Nagaraj, Cuixia Tian, et al.
Muscle & Nerve|December 23, 2025
Acute Adverse Events Following Intravenous Bisphosphonate Infusion Are Uncommon in Patients With Duchenne Muscular Dystrophy Previously Treated With Oral BisphosphonatesNat Nasomyont, Pitchamol Vilaisaktipakorn, Halley Wasserman, et al.
Journal of Neuroscience Methods|May 26, 2012
Effects of 30Hz θ burst transcranial magnetic stimulation on the primary motor cortexSteve W Wu, Nasrin Shahana, David A Huddleston, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|January 17, 2004
Tic reduction with risperidone versus pimozide in a randomized, double-blind, crossover trialDonald L Gilbert, J Robert Batterson, Gopalan Sethuraman, et al.
Pediatrics|January 28, 2009
Effects of sleep deprivation on the pediatric electroencephalogramSteven T DeRoos, Kipp L Chillag, Martina Keeler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2008
A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31Donald L Gilbert, Elizabeth J Leslie, Mehdi Keddache, et al.
Pediatric Neurology|December 6, 2017
Child Neurology Residency Program Directors and Program Coordinators 2016 Workforce SurveyDonald L Gilbert, Julie A LaBare, Karen Keough, et al.
The Journal of Nutritional Biochemistry|January 31, 2026
SIRT3 ameliorates hepatic inflammation, oxidative stress, and fibrosis in HFD- or MCD diet-fed miceHuifang Lv, Wenyue Sun, Cuixia Tian, et al.
Neurology. Genetics|July 22, 2024
Compound Heterozygous Variants of <i>GOSR2</i> Associated With Congenital Muscular Dystrophy and Progressive Myoclonus Epilepsy: A Case ReportMonica S Arroyo, Christine Fuller, Elizabeth K Schorry, et al.
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