Results 91 to 100 of about 8,162 (152)

A Novel SLC9A3R1 Mutation as a Rare Cause of Infantile Hypercalcemia. [PDF]

open access: yesCureus
Ravi Kumar P   +4 more
europepmc   +1 more source

Clinical Approaches and Emerging Therapeutic Horizons in Primary Hyperoxaluria. [PDF]

open access: yesJ Clin Med
Martínez-Galindo R   +7 more
europepmc   +1 more source

Targeting Hypercalciuria in SLC34A1-Related Disorders: Impact of Oral Phosphate Therapy and Novel Genetic Insights in Pediatric Case Series. [PDF]

open access: yesCalcif Tissue Int
Turan I   +12 more
europepmc   +1 more source

[Nephrocalcinosis].

open access: yesRevista chilena de pediatria, 1989
F, Puga, A, Bahamondes, J, Poniachik
openaire   +1 more source

Genetic causes of nephrolithiasis and nephrocalcinosis in a pediatric population in Saudi Arabia. [PDF]

open access: yesPediatr Nephrol
Alsubaie H   +8 more
europepmc   +1 more source

The domestic pig as a translational model of hyperoxaluria: a pilot study of acute and chronic sodium oxalate infusion. [PDF]

open access: yesFront Physiol
Jacek T   +10 more
europepmc   +1 more source

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