Found: 10
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The Molecular Genetics of Gordon Syndrome.
- Published in:
- Genes, 2019, v. 10, n. 12, p. 986, doi. 10.3390/genes10120986
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- Article
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease.
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- Nephrology Dialysis Transplantation, 2023, v. 38, n. 2, p. 271, doi. 10.1093/ndt/gfab268
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- Article
Investigation and management of renal stone disease.
- Published in:
- Nephrology Dialysis Transplantation, 2017, v. 32, n. 12, p. 1984, doi. 10.1093/ndt/gfx306
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- Article
Biallelic variants in TTC21B as a rare cause of early‐onset arterial hypertension and tubuloglomerular kidney disease.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2022, v. 190, n. 1, p. 109, doi. 10.1002/ajmg.c.31964
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- Article
Large Retroperitoneal Haemorrhage Following Cyst Rupture in a Patient with Autosomal Dominant Polycystic Kidney Disease.
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- Case Reports in Nephrology, 2017, p. 1, doi. 10.1155/2017/4653267
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- Article
Explaining Alport syndrome—lessons from the adult nephrology clinic.
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- Journal of Rare Diseases, 2024, v. 3, n. 1, p. 1, doi. 10.1007/s44162-024-00036-z
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- Article
Finerenone and other future therapeutic options for Alport syndrome.
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- Journal of Rare Diseases, 2023, v. 2, n. 1, p. 1, doi. 10.1007/s44162-023-00022-x
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- Article
UMOD and you! Explaining a rare disease diagnosis.
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- Journal of Rare Diseases, 2022, v. 1, n. 1, p. 1, doi. 10.1007/s44162-022-00005-4
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- Article
SGLT2 inhibitors - a potential treatment for Alport syndrome.
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- Clinical Science, 2020, v. 134, n. 4, p. 379, doi. 10.1042/CS20191276
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- Article
Genetic analysis and outcomes of Omani children with steroid‐resistant nephrotic syndrome.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 9, p. 1, doi. 10.1002/mgg3.2201
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- Article