Bone impairment in primary hyperoxaluria: a review.

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Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.

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P2860

Bone impairment in primary hyperoxaluria: a review.

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2015年の論文

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Bone impairment in primary hyperoxaluria: a review.

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type

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Bone impairment in primary hyperoxaluria: a review.

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Bone impairment in primary hyperoxaluria: a review.

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P1476

Bone impairment in primary hyperoxaluria: a review.

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Georges Boivin

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Pierre Cochat

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P2860

Mutations in DHDPSL are responsible for primary hyperoxaluria type III

Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer

Oral findings associated with primary hyperoxaluria type I.

Characteristics and outcomes of children with primary oxalosis requiring renal replacement therapy

The consequences of chronic kidney disease on bone metabolism and growth in children.

Primary hyperoxaluria type 1: still challenging!

Skeletal features of primary hyperoxaluria type 1, revisited

Oxalate in renal stone disease: the terminal metabolite that just won't go away.

Technical approach to iliac crest biopsy.

Oxalosis in primary hyperoxaluria in infancy : Report of a case in a 3-month-old baby. Follow-up for 3 years and review of literature.

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s00467-015-3048-z

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1-6

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scholarly article

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10.1007/S00467-015-3048-Z

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Justine Bacchetta

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2015-01-29T00:00:00Z

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271596977

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25631241

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Bone impairment in primary hyperoxaluria: a review.

about

P2860

P2860

Bone impairment in primary hyperoxaluria: a review.

description

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P1476

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P2860

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