D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity? von Van Der Knaap, M. S., Jakobs, C., Hoffmann, G. F., Nyhan, W. L., Renier, W. O., Smeitink, J. A. M., Catsman-Berrevoets, C. E., Hjalmarson, O., Vallance, H., Sugita, K., Bowe, C. M., Herrin, J. T., Craigen, W. J., Buist, N. R. M., Brookfield, D. S. K., Chalmers, R. A.

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Varicella in pediatric renal transplant recipients von LYNFIELD, R, HERRIN, J. T, RUBIN, R. H

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Autosomal recessive polycystic kidney disease: long-term sonographic findings in patients surviving the neonatal period von Blickman, JG, Bramson, RT, Herrin, JT

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Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger von Jarolim, P, Shayakul, C, Prabakaran, D, Jiang, L, Stuart-Tilley, A, Rubin, H L, Simova, S, Zavadil, J, Herrin, J T, Brouillette, J, Somers, M J, Seemanova, E, Brugnara, C, Guay-Woodford, L M, Alper, S L

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Effects of ureteral function on assessment of hydronephrosis von Herrin, J T

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Effects of interferon-alpha on cytomegalovirus reactivation syndromes in renal-transplant recipients von Hirsch, M.S, Schooley, R.T, Cosimi, A.B, Russell, P.S, Delmonico, F.L

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Near-death experiences in the very young von HERZOG, DAVID B, HERRIN, JOHN T

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Pulmonary dysplasia, Denys-Drash syndrome and wilms tumor 1 gene mutation in twins von DHARNIDHARKA, Vikas R, RUTESHOUSER, E. Cristy, ROSEN, Seymour, KOZAKEWICH, Harry, HARRIS, H. William, HERRIN, John T, HUFF, Vicki

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Parathyroid surgery in patients with renal failure von DELMONICO, F. L, WANG, C. A, RUBIN, N. T, FANG, L. S, HERRIN, J. T, COSIMI, A. B

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Coexisting nephrolithiasis and cholelithiasis in premature infants von Blickman, J G, Herrin, J T, Cleveland, R H, Jaramillo, D

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Increased intraabdominal pressure and anuria in the newborn von Goldstein, Brahm, Herrin, John T., David Todres, I.

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Management of Children with Progressive Renal Failure von Herrin, John T

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Genital abnormalities in females with Bardet-Biedl syndrome von Stoler, Joan M., Herrin, John T., Holmes, Lewis B.

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Percutaneous ultrasonic lithotripsy of symptomatic renal calculi in children von PAPANICOLAOU, N, PFISTER, R. C, YOUNG, H. H. II, YODER, I. C, HERRIN, J. T

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Treatment of acute renal allograft rejection with OKT3 monoclonal antibody von Cosimi, A B, Burton, R C, Colvin, R B, Goldstein, G, Delmonico, F L, LaQuaglia, M P, Tolkoff-Rubin, N, Rubin, R H, Herrin, J T, Russell, P S

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Pediatric renal transplantation von Herrin, John T.

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Peritoneal dialysis in the reduction of blood ammonia levels in a case of hyperammonaemia von Herrin, J. T., McCredie, D. A.

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Studies on the pathophysiology of encephalopathy in Reye's syndrome; Hyperammonemia in Reye's syndrome von Shannon, D C, De Long, R, Bercu, B, Glick, T, Herrin, J T, Moylan, F M, Todres, I D

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Ketamine induction in poor-risk patients von Nettles, D C, Herrin, T J, Mullen, J G

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Glomerulopathy Associated with Cytomegalovirus Viremia in Renal Allografts von Richardson, Walter P, Colvin, Robert B, Cheeseman, Sarah H, Tolkoff-Rubin, Nina E, Herrin, John T, Cosimi, A. Benedict, Collins, A. Bernard, Hirsch, Martin S, McCluskey, Robert T, Russell, Paul S, Rubin, Robert H

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