Metabolite diagnosis of primary hyperoxaluria type 3

Simultaneous analysis of urinary metabolites for preliminary identification of primary hyperoxaluria

(2016) Oliver Clifford-Mobley et al.   ANNALS OF CLINICAL BIOCHEMISTRY

Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria

(2015) K. Hopp et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Renal function can be impaired in children with primary hyperoxaluria type 3

(2015) Lise Allard et al.   PEDIATRIC NEPHROLOGY

Primary hyperoxalurias: diagnosis and treatment

(2014) Efrat Ben-Shalom et al.   PEDIATRIC NEPHROLOGY

4-Hydroxy-2-oxoglutarate aldolase inactivity in primary hyperoxaluria type 3 and glyoxylate reductase inhibition

(2012) Travis J. Riedel et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

(2012) Bodo B Beck et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Primary hyperoxaluria type III—a model for studying perturbations in glyoxylate metabolism

(2012) Ruth Belostotsky et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Primary Hyperoxaluria Type III Gene HOGA1 (Formerly DHDPSL) as a Possible Risk Factor for Idiopathic Calcium Oxalate Urolithiasis

(2011) C. G. Monico et al.   Clinical Journal of the American Society of Nephrology

Mutations in DHDPSL Are Responsible For Primary Hyperoxaluria Type III

(2010) Ruth Belostotsky et al.   AMERICAN JOURNAL OF HUMAN GENETICS