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Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
Journal of Clinical Investigation, 11/10/08
Broer S et al. - Although recognized as apparently simple Mendelian disorders, IG and HG exhibit complex molecular explanations depending on a major gene and accompanying modifier genes.
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Lactic Acidosis Associated With Metformin in a Patient With Type 2 Diabetes With No Contraindication
The Endocrinologist, 11/13/09
Sodium bicarbonate—the bicarbonate challenge test in metabolic acidosis: A practical consideration
Current Anaesthesia and Critical Care, 11/30/09
Feasibility of combined treatment with enalapril and candesartan in advanced chronic kidney disease
Nephrology Dialysis Transplantation, 11/17/09
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