TY  - JOUR
AU  - Nieto-Vega, Francisco Antonio
AU  - Martin-Masot, Rafael
AU  - Rodriguez-Azor, Begoña
AU  - Martinez-Rivera, Veronica
AU  - Herrador-Lopez, Marta
AU  - Navas-Lopez, Victor Manuel
PY  - 2020
DO  - 10.1007/s00467-020-04615-2
UR  - http://hdl.handle.net/10668/15830
T2  - Pediatric nephrology (Berlin, Germany)
AB  - Hyperoxaluria can be divided into two categories: primary and secondary. Primary hyperoxaluria is the result of an inherited hepatic enzyme deficiency leading to an increased endogenous production of oxalate, and usually exhibits excessively high...
LA  - en
PB  - Springer
KW  - Nephrocalcinosis
KW  - Nephrolithiasis
KW  - Hyperoxaluria
KW  - Hyperparathyroidism
KW  - Celiac disease
KW  - Malabsorption syndrome
KW  - Oxalates
KW  - Hyperoxaluria, Primary
KW  - Malabsorption Syndromes
KW  - Gastrointestinal Diseases
KW  - Intestinal Absorption
TI  - A rare cause of nephrocalcinosis in an infant: Answers.
TY  - research article
VL  - 36
ER  -