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UnknownFAT1 mutations cause a glomerulotubular nephropathy.
Not available
S-EPMC4770090 | biostudies-literature
UnknownAdvillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome.
Not available
S-EPMC5707164 | biostudies-literature
UnknownMutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.
Not available
S-EPMC5958119 | biostudies-literature
UnknownCOQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.
Not available
S-EPMC3083770 | biostudies-literature
UnknownWhole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Not available
S-EPMC5753307 | biostudies-literature
UnknownWhole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Not available
S-EPMC6115658 | biostudies-literature
UnknownA single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Not available
S-EPMC4446877 | biostudies-literature
UnknownMutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Not available
S-EPMC5819591 | biostudies-literature
UnknownA prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts.
Not available
S-EPMC12056793 | biostudies-literature
UnknownEmpagliflozin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial.
Not available
S-EPMC10957483 | biostudies-literature
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