Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in Germany.

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Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in Germany.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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P1476

Update on Hereditary Kidney St ...... l Patient Registry in Germany.

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P2093

Anna Seidel

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Bernd Hoppe

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Jan Halbritter

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Luise Müller

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Ria Schönauer

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P2860

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II

Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

Mutations in DHDPSL are responsible for primary hyperoxaluria type III

Molecular identification of a renal urate anion exchanger that regulates blood urate levels

NHERF1 mutations and responsiveness of renal parathyroid hormone

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine

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scholarly article

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10.3389/FPED.2018.00047

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P478

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2018-03-07T00:00:00Z

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29564324

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5850730

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