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Current Opinion in Pediatrics|April 1, 2026
Treatment advances for Duchenne muscular dystrophyAlexander Zygmunt, Cuixia Tian
Neuromuscular Disorders : NMD|March 27, 2026
From case to caution: hyponatremia in a patient with Duchenne muscular dystrophy on vamorolone and lessons for cliniciansChelsea Murphy, Nat Nasomyont, Cuixia Tian, et al.
Muscle & Nerve|September 18, 2024
The impact of genotype on age at loss of ambulation in individuals with Duchenne muscular dystrophy treated with corticosteroids: A single-center study of 555 patientsAlexander Zygmunt, Brenda Wong, David Moon, et al.
Pediatric Neurology|June 1, 2026
Fatal Fat Embolism Syndrome Without Recognized Fracture in Patients With Duchenne Muscular Dystrophy: Two Case ReportsCameron A Wade, Chet Villa, Larry B Goldstein, et al.
Blood|November 2, 2002
The function of the bcl-x promoter in erythroid progenitor cellsCuixia Tian, Paul Gregoli, Maurice Bondurant
Journal of Clinical Neuromuscular Disease|February 26, 2025
RNA Sequencing Confirms the Pathogenicity of a Novel FHL1 Deletion in a Kinship With Emery-Dreifuss Muscular DystrophyChinmayee B Nagaraj, Cuixia Tian, Hani Kushlaf
Pediatric Neurology|April 22, 2019
White Matter Lesions Detected by Magnetic Resonance Imaging in Neonates and Children With Congenital Myotonic DystrophyLindsay M Peglar, Usha D Nagaraj, Cuixia Tian, et al.
Seminars in Pediatric Neurology|December 8, 2023
Sleep in pediatric neuromuscular disordersJohn E Pascoe, Alexander Zygmunt, Zarmina Ehsan, et al.
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.
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