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International Journal of Neonatal Screening|August 27, 2021
Diagnosis of Classic Homocystinuria in Two Boys Presenting with Acute Cerebral Venous Thrombosis and Neurologic Dysfunction after Normal Newborn ScreeningAlexander Asamoah, Sainan Wei, Kelly E Jackson, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|November 10, 2021
Sustained-release capsules coated via thermoforming techniquesLian Shen, Xiaohong Yu, Hui Fu, et al.
AJP Reports|October 24, 2015
Frontofacionasal Dysplasia in a Newborn with a De Novo Duplication of 7p15.2-p15.1Tamer Mansour, Sainan Wei, Michael Netzloff, et al.
Nanoscale|October 10, 2025
CoFe-NaYF4:Yb/Er@SMPC derived carbon film: integrated precise stimuli-responsive NIR photothermal sensing and shape-memory performanceLuning Sun, Yunxiang Yuan, Hongchao Zhang, et al.
Journal of Geriatric Oncology|January 30, 2014
HER2 status in elderly women with breast cancerHeather S Laird-Fick, Joseph C Gardiner, Hemasri Tokala, et al.
Biomedicines|August 29, 2024
NSD3::NUTM1 Fusion Sarcoma Mimicking Malignant Peripheral Nerve Sheath Tumor with Prolonged SurvivalJing Di, Ali M Alhaidary, Chi Wang, et al.
The Journal of Molecular Diagnostics : JMD|November 30, 2024
The Validation of Digital PCR-Based Minimal Residual Disease Detection for the Common Mutations in IDH1 and IDH2 Genes in Patients with Acute Myeloid LeukemiaJing Di, Tao Sheng, Ranjana Arora, et al.
Biomedicines|November 27, 2024
Prognostic Significance and Treatment Response Associations of Genetic Mutations in Chronic Myelomonocytic Leukemia: A Retrospective Cohort StudyJing Di, Leonard N Yenwongfai, Talal Arshad, et al.
Leukemia Research|January 27, 2020
Acute undifferentiated leukemia: data on incidence and outcomes from a large population-based databaseAyman Qasrawi, Victor Gomes, Charles Andrew Chacko, et al.
Molecular Genetics and Metabolism Reports|June 28, 2017
Corrigendum to "First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children" [Mol. Genet. Metab. Rep. 2 (2016) 81-84]Danika Nadeen Senanayake, Eresha A Jasinge, Kirit Pindolia, et al.
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