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Pediatric Nephrology (Berlin, Germany)|August 1, 1994
Renal artery stenosis associated with melorheostosisJ H Iglesias, A L Stocks, D R Pena, et al.
Pediatric Nephrology (Berlin, Germany)|November 5, 1997
A new point mutation in a hypoxanthine phosphoribosyltransferase-deficient patientR I Hidalgo-Laos, A Kedar, C A Williams, et al.
Child Nephrology and Urology|January 1, 1990
Renal calculi in pediatric renal transplant recipientsD R Pena, R S Fennell, A Iravani, et al.
The Journal of Clinical Endocrinology and Metabolism|April 9, 2004
Dichloroacetate therapy attenuates the blood lactate response to submaximal exercise in patients with defects in mitochondrial energy metabolismG E Duncan, L A Perkins, D W Theriaque, et al.
The Journal of Pediatrics|January 8, 1999
The importance of cerebrospinal fluid lactate in the evaluation of congenital lactic acidosisP W Stacpoole, S T Bunch, R E Neiberger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excessR C Wilson, M D Harbison, Z S Krozowski, et al.
The Journal of Clinical Endocrinology and Metabolism|July 14, 1998
Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excessS Dave-Sharma, R C Wilson, M D Harbison, et al.
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