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Ma Lili

As seen in: Frontiers, Arthritis Research & Therapy, Journal of Medical Case Reports
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Articles by Ma Lili

Pulmonary artery thrombosis in preterm infants born to a diabetic mother: a case report - Journal of Medical Case Reports

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By Ma Lili, Yin Xiangyun, Xi Hongmin, Li Liangliang, Liu Weigang, Li Xianghong
| Journal of Medical Case Reports Verified
References Kenny D, Tsai-Goodman B. Neonatal arterial thrombus mimicking congenital heart disease. Arch Dis Child Fetal Neonatal Ed. 2007;92:59–61. https://doi.org/10.1136/abc. Article Google Scholar Bacciedoni V, Attie M, Donato H. Thrombosis in newborn infants. Arch Argent Pediatr. 2016;114(02):159–66. https://doi.org/10.5546/aap. Article PubMed Google Scholar Paes BA, Nagel K, Sunak I, Rashish G, Chan AK. Thrombosis and Hemostasis in Newborns (THiN) Group.
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High level of serum complement 3 is a risk factor for vascular stenosis progression in TA patients receiving tocilizumab: a prospective observational study | Arthritis Research & Therapy | Full Text

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By Chen Rongyi, Ma Lingying, Ma Lili, Sun Ying, Dai Xiaojuan, Wang Jinghua, Dai Xiaomin, Chen Huiyong, Jiang Lindi
| Arthritis Research & Therapy Verified
This prospective observational study focuses on VSP in TA patients treated with tocilizumab. Although tocilizumab was effective in alleviating inflammation and disease activity, approximately 47.3% of TA patients receiving tocilizumab showed VSP during the follow-up period. This finding was consistent with those of previous reports, which did not attract enough attention (Summarized in Supplementary Table S5). Furthermore, C3 was a predictive factor for VSP, with an AUC of 0.825 in 1 year.
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Case Report: Real NPSLE? A patient with systemic sclerosis overlapping systemic lupus erythematosus presenting as epilepsy

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By Minrui Liang, Nan Che, Ma Lili
| Frontiers
Highlights ● NPSLE is not the only answer to CNS symptoms in patients with SLE overlapping SSc. ● Distinguishing between RPLS due to SRC and NPSLE is critical for the patient’s prognosis. A 17-year-old female patient with a one-and-a-half-year history of SSc and SLE was admitted to our rheumatology department.
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