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KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort [2016]
Gitelman syndrome: a review of clinical features, genetic diagnosis and therapeutic management [2016]
Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis [2016]
A Single Nucleotide Polymorphism in the Il17ra Promoter Is Associated with Functional Severity of Ankylosing Spondylitis [2016]
An elderly Jervell and Lange-Nielsen patient heterozygous compound for two new KCNQ1 mutations [2016]
The TNFRSF1B rs1061622 polymorphism (p.M196R) is associated with biological drug outcome in Psoriasis patients [2015]
The donor ABCB1 (MDR-1) C3435T polymorphism is a determinant of the graft glomerular filtration rate among tacrolimus treated kidney transplanted patients [2015]
The Cw6 and late-cornified envelope genotype plays a significant role in anti-tumor necrosis factor response among psoriatic patients [2015]
Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study [2015]
Next generation sequencing search for uromodulin gene variants related with impaired renal function [2015]
Molecular findings potentially linked to the increased height of growth plate chondrocytes induced by growth hormone (gh) treatment in uremia [2015]
MAPT H1 haplotype is associated with late-onset Alzheimer's disease risk in APOE e 4 noncarriers: Results from the dementia genetics Spanish consortium [2015]
Influence of Fcγ receptor polymorphisms on response to anti-tumor necrosis factor treatment in psoriasis [2015]
Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum? [2015]
Cysteamine (Cystagon (R)) adherence in patients with cystinosis in Spain: successful in children and a challenge in adolescents and adults [2015]
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