Works matching IS 21947228 AND DT 2019 AND VI 47 AND IP 1
Results: 13
Urinary proteome in inherited nephrolithiasis.
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- Urolithiasis, 2019, v. 47, n. 1, p. 91, doi. 10.1007/s00240-018-01104-y
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- Article
Inherited proximal tubular disorders and nephrolithiasis.
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- Urolithiasis, 2019, v. 47, n. 1, p. 35, doi. 10.1007/s00240-018-01103-z
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Cystinuria: genetic aspects, mouse models, and a new approach to therapy.
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- Urolithiasis, 2019, v. 47, n. 1, p. 57, doi. 10.1007/s00240-018-1101-7
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Empirical therapy or precision medicine for kidney stone formers in the ‘-omics’ era?
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- Urolithiasis, 2019, v. 47, n. 1, p. 1, doi. 10.1007/s00240-018-1099-x
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- Article
Nephrolithiasis secondary to inherited defects in the thick ascending loop of henle and connecting tubules.
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- Urolithiasis, 2019, v. 47, n. 1, p. 43, doi. 10.1007/s00240-018-1097-z
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Calcium-sensing receptor: evidence and hypothesis for its role in nephrolithiasis.
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- Urolithiasis, 2019, v. 47, n. 1, p. 23, doi. 10.1007/s00240-018-1096-0
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Heritable traits that contribute to nephrolithiasis.
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- Urolithiasis, 2019, v. 47, n. 1, p. 5, doi. 10.1007/s00240-018-1095-1
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Genetics of common complex kidney stone disease: insights from genome-wide association studies.
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- Urolithiasis, 2019, v. 47, n. 1, p. 11, doi. 10.1007/s00240-018-1094-2
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Recent advances in the identification and management of inherited hyperoxalurias.
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- Urolithiasis, 2019, v. 47, n. 1, p. 79, doi. 10.1007/s00240-018-1093-3
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Living kidney donation from people at risk of nephrolithiasis, with a focus on the genetic forms.
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- Urolithiasis, 2019, v. 47, n. 1, p. 115, doi. 10.1007/s00240-018-1092-4
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Precision medicine in renal stone-formers.
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- Urolithiasis, 2019, v. 47, n. 1, p. 99, doi. 10.1007/s00240-018-1091-5
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Empiric therapy for kidney stones.
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- Urolithiasis, 2019, v. 47, n. 1, p. 107, doi. 10.1007/s00240-018-1090-6
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- Article
Molecular basis of primary hyperoxaluria: clues to innovative treatments.
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- Urolithiasis, 2019, v. 47, n. 1, p. 67, doi. 10.1007/s00240-018-1089-z
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- Article