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鹿鸣
Lv2
110 积分
2023-06-05 加入
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Hypouricaemia in a patient with hereditary xanthinuria type I
13天前
已完结
Common Defects of ABCG2, a High-Capacity Urate Exporter, Cause Gout: A Function-Based Genetic Analysis in a Japanese Population
1个月前
已完结
TBX20loss-of-function variants in families with left ventricular non-compaction cardiomyopathy
2个月前
已完结
Familial chylomicronemia syndrome caused by compound heterozygous mutation of lipoprotein lipase gene: A case report and review of literature
2个月前
已完结
Dilated cardiomyopathy and new 16 bp deletion in exon 44 of the dystrophin gene: The possible role of repeated motifs in mutation generation
2个月前
已完结
A Novel Exon 2 Deletion Mutation in the GRXCR1 Gene Associated With Non-Syndromic Hearing Loss: A Case Report and Review of Literatures
2个月前
已完结
Emerging Urate-Lowering Drugs and Pharmacologic Treatment Strategies for Gout: A Narrative Review
3个月前
已完结
Uric acid in health and disease: From physiological function to pathogenic mechanism
3个月前
已完结
U-shaped association of uric acid to overall-cause mortality and its impact on clinical management of hyperuricemia
3个月前
已完结
A novel mutation in a patient with familial renal hypouricemia type 2
4个月前
已完结
The anatomical locations of postoperative pain and their recovery trajectories following Posterior Spinal Fusion (PSF) surgery in Adolescent Idiopathic Scoliosis (AIS) patients
11个月前
已采纳
PGE2经EP4R-EGFR-Gab1信号传导通路促进视网膜新生血管形成的作用及机制研究
11个月前
已采纳
鼻腔冲洗不良反应的原因分析及预防
11个月前
已采纳
One stage anterior-posterior approach for traumatic atlantoaxial instability combined with subaxial cervical spinal cord injury
11个月前
已采纳
标题错误
6个月前
消息有误【积分已退回】
10个月前
感谢
10个月前
已找到【积分已退回】
10个月前
帮大忙了,感谢
11个月前
感谢,帮大忙了,么么哒,速度真快,点赞
11个月前
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