Lv71
3588 积分 2025-01-25 加入
星形胶质细胞在蛛网膜下腔出血中的作用研究进展
1小时前
已完结
Rapamycin alleviates mitochondrial dysfunction in anti-NMDAR encephalitis mice
1个月前
已完结
Blood and CSF findings of cellular immunity in anti-NMDAR encephalitis
1个月前
已完结
Impact of inhalation exposure to cigarette smoke on the pathogenesis of pulmonary hypertension primed by monocrotaline in rats
2个月前
已完结
Decoding the complexity: mechanistic insights into comorbidities in idiopathic pulmonary fibrosis
2个月前
已关闭
Adverse effect of smoking on cross‐sectional area of small pulmonary vessel and arterial stiffness in healthy smokers without COPD
2个月前
已完结
Pathophysiology, diagnosis, prognosis and treatment of pulmonary hypertension associated with chronic lung disease
2个月前
已完结
Pulmonale Hypertonie bei Lungenerkrankungen und/oder Hypoxie
2个月前
已关闭
Smoking history and pulmonary arterial hypertension: Demographics, onset, and outcomes
2个月前
已完结
Pulmonary Hypertension
2个月前
已完结
Electromodulation of human monocyte-derived macrophages drives a regenerative phenotype and impedes inflammation
2个月前
已采纳
Evaluation of Hard Tissue Changes in Skeletally Matured Patients with Maxillary Transverse Discrepancy Treated by Rotterdam Palatal Distractor
2个月前
已采纳
Joint effects of predatory protists and predatory bacteria on driving the evolution of bacterial antibiotic resistance
2个月前
已采纳
Case Report: DARS Mutations Responsible for Hypomyelination With Brain Stem and Spinal Cord Involvement and Leg Spasticity
3个月前
已采纳
A rare loss-of-function genetic mutation suggest a role of dermcidin deficiency in hidradenitis suppurativa pathogenesis
3个月前
已采纳
The clinical characteristics and genotype analysis of LAMB2 gene mutation
3个月前
已采纳
Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy
3个月前
已采纳
Turner syndrome and postpubertal Empty sella syndrome: a case report and literature review
3个月前
已采纳
Clinical characteristics of familial dysalbuminemic hyperthyroxinemia in Chinese patients and comparison of free thyroxine in three immunoassay methods
3个月前
已采纳
Novel compound heterozygous CCDC40 mutations in a familial case of primary ciliary dyskinesia
3个月前
已采纳
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