Lv538
1390 积分 2021-10-30 加入
Narrowing the Genomic Region of Autosomal-Dominant Congenital Generalized Hypertrichosis Terminalis
2个月前
已完结
Dermatopathological features and successful treatment with topical antioxidant for ichthyosiform lesions in Mitchell syndrome caused by an ACOX1 variant
2个月前
已完结
Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorder
2个月前
已完结
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformation
2个月前
已完结
A loss-of-function variant in KLF4 affecting zinc finger motifs causes progressive symmetric erythrokeratodermia
2个月前
已完结
A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataracts
2个月前
已完结
Risk Factors for Primary Angle-closure Glaucoma: A Systematic Review and Meta-Analysis of 45 Studies
1年前
已完结
Recombinant human C1 esterase inhibitor for prophylaxis of hereditary angio-oedema: a phase 2, multicentre, randomised, double-blind, placebo-controlled crossover trial
1年前
已完结
85 Clinical Efficacy of Recombinant Human C1 Inhibitor in Patients with Acute Hereditary Angioedema Attacks
1年前
已完结
Noise-Induced Hearing Loss Treatment: Systematic Review and Meta-analysis
1年前
已完结
皖公网安备34019202002308
