Pages that link to "Q36108478"

The following pages link to The primary hyperoxalurias: an algorithm for diagnosis (Q36108478):

Displaying 24 items.

• A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2 (Q24306240) (← links)
• The comparability of oxalate excretion and oxalate:creatinine ratio in the investigation of primary hyperoxaluria: review of data from a referral centre. (Q30797651) (← links)
• Hereditary causes of kidney stones and chronic kidney disease (Q34066169) (← links)
• Transplantation Outcomes in Primary Hyperoxaluria (Q34247162) (← links)
• Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencing (Q34987476) (← links)
• Primary and secondary hyperoxaluria: Understanding the enigma (Q35567868) (← links)
• A rare case of hyperoxaluria presenting with acute liver injury and stone-free kidney injury (Q36061758) (← links)
• Hyperoxaluria and systemic oxalosis: current therapy and future directions (Q36613873) (← links)
• Genetic determinants of urolithiasis (Q37512167) (← links)
• Cardiac abnormalities in primary hyperoxaluria (Q37797844) (← links)
• An update on primary hyperoxaluria (Q38017938) (← links)
• Primary hyperoxalurias: diagnosis and treatment (Q38292247) (← links)
• An expanded syndrome of dRTA with hearing loss, hyperoxaluria and beta2-microglobulinuria (Q40338902) (← links)
• Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome (Q43218013) (← links)
• Autopsy findings of a case with oxalosis (Q43279756) (← links)
• Plasma oxalate level in pediatric calcium stone formers with or without secondary hyperoxaluria (Q46138323) (← links)
• Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center. (Q46196970) (← links)
• The urinary metabolomics profile of an Italian autistic children population and their unaffected siblings (Q50303972) (← links)
• Molecular analysis of the AGXT gene in patients suspected with hyperoxaluria type 1 and three novel mutations from Turkey. (Q51029593) (← links)
• Genetic Causes of Kidney Stones and Kidney Failure (Q58118152) (← links)
• Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria (Q61700135) (← links)
• Nephrolithiasis (Q81295660) (← links)
• The primary hyperoxalurias (Q83370521) (← links)
• Primary Hyperoxaluria-Imaging of Renal Oxalosis (Q90484683) (← links)