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Preclinical Detection of Early Glomerular Injury in Children with Kidney Diseases—Independently of Usual Markers of Kidney Impairment and Inflammation.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 17, p. 9320, doi. 10.3390/ijms25179320
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- Article
Ratio of Urinary Proteins to Albumin Excretion Shifts Substantially during Progression of the Podocytopathy Alport Syndrome, and Spot Urine Is a Reliable Method to Detect These Pathologic Changes.
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- Cells (2073-4409), 2023, v. 12, n. 9, p. 1333, doi. 10.3390/cells12091333
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- Article
Sodium-Glucose Cotransporter-2 Inhibitors in Patients with Hereditary Podocytopathies, Alport Syndrome, and FSGS: A Case Series to Better Plan a Large-Scale Study.
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- Cells (2073-4409), 2021, v. 10, n. 7, p. 1815, doi. 10.3390/cells10071815
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- Article
Genotype–phenotype correlations and nephroprotective effects of RAAS inhibition in patients with autosomal recessive Alport syndrome.
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- Pediatric Nephrology, 2021, v. 36, n. 9, p. 2719, doi. 10.1007/s00467-021-05040-9
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- Article
Okuläre Veränderungen bei Patienten mit Alport-Syndrom – ein Update.
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- Die Ophthalmologie, 2023, v. 120, n. 6, p. 645, doi. 10.1007/s00347-022-01805-1
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- Article
Lifelong effect of therapy in young patients with the COL4A5 Alport missense variant p.(Gly624Asp): a prospective cohort study.
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- Nephrology Dialysis Transplantation, 2022, v. 37, n. 12, p. 2496, doi. 10.1093/ndt/gfac006
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- Article
Precise variant interpretation, phenotype ascertainment, and genotype–phenotype correlation of children in the EARLY PRO‐TECT Alport trial.
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- Clinical Genetics, 2021, v. 99, n. 1, p. 143, doi. 10.1111/cge.13861
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- Article
Validation of a Prospective Urinalysis-Based Prediction Model for ICU Resources and Outcome of COVID-19 Disease: A Multicenter Cohort Study.
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- Journal of Clinical Medicine, 2021, v. 10, n. 14, p. 3049, doi. 10.3390/jcm10143049
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- Article
Characterization of Sensorineural Hearing Loss in Children with Alport Syndrome.
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- Life (2075-1729), 2020, v. 10, n. 12, p. 360, doi. 10.3390/life10120360
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- Article