Search Results - "Herrin, J. T."

D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity? by 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.

“…D‐2‐Hydroxyglutaric aciduria has been observed in patients with extremely variable clinical symptoms, creating doubt about the existence of a disease entity…”
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Varicella in pediatric renal transplant recipients by LYNFIELD, R, HERRIN, J. T, RUBIN, R. H

“…As of November 1991, 8 of 83 children who had received renal transplants at Massachusetts General Hospital since January 1979 required admission for primary…”
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Autosomal recessive polycystic kidney disease: long-term sonographic findings in patients surviving the neonatal period by Blickman, JG, Bramson, RT, Herrin, JT

“…We studied the sonographic findings and the changes in renal function seen on long-term follow-up of children who had the initial diagnosis of autosomal…”
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Effects of ureteral function on assessment of hydronephrosis by Herrin, J T

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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 by 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

“…Distal renal tubular acidosis (dRTA) is characterized by defective urinary acidification by the distal nephron. Cl-/HCO3- exchange mediated by the AE1 anion…”
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Infantile polycystic disease of the liver and kidneys by Gang, D L, Herrin, J T

“…Kidney and liver tissue from eleven patients with recessively inherited infantile polycystic disease (IPCD) were examined to document the extent of renal…”
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Effects of interferon-alpha on cytomegalovirus reactivation syndromes in renal-transplant recipients by Hirsch, M S, Schooley, R T, Cosimi, A B, Russell, P S, Delmonico, F L, Tolkoff-Rubin, N E, Herrin, J T, Cantell, K, Farrell, M L, Rota, T R, Rubin, R H

“…We have previously demonstrated that six weeks of prophylaxis with interferon-alpha delays cytomegalovirus excretion and decreases viremia in recipients of…”
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Near-death experiences in the very young by Herzog, D B, Herrin, J T

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

“…A subtotal parathyroidectomy was performed in 32 patients with hyperparathyroidism and renal dysfunction. Minimal long-term sequelae were observed [two…”
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Coexisting nephrolithiasis and cholelithiasis in premature infants by Blickman, J G, Herrin, J T, Cleveland, R H, Jaramillo, D

“…Though the coexistence of nephrolithiasis and cholelithiasis in premature infants is extremely rare, we report four patients seen in a two year period. All…”
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Increased intraabdominal pressure and anuria in the newborn by Goldstein, B, Herrin, J T, Todres, I D

“…Elevated intraabdominal pressure as a cause of anuria in the critically ill newborn with ascites should be considered after hypovolemia and other causes of…”
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Percutaneous ultrasonic lithotripsy of symptomatic renal calculi in children by PAPANICOLAOU, N, PFISTER, R. C, YOUNG, H. H. II, YODER, I. C, HERRIN, J. T

“…Percutaneous ultrasonic lithotripsy of upper urinary tract lithiasis is a well-established procedure in adults. We successfully applied this technique to…”
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Genital abnormalities in females with Bardet-Biedl syndrome by Stoler, J M, Herrin, J T, Holmes, L B

“…The major manifestations of the Bardet-Biedl syndrome are digital anomalies, tapetoretinal degeneration, obesity, renal abnormalities, and hypogenitalism…”
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Management of Children with Progressive Renal Failure by Herrin, John T

“…The strategy of management in childhood renal failure is to integrate available therapeutic modalities with the natural history of the disease in such a manner…”
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Pulmonary dysplasia, Denys-Drash syndrome and wilms tumor 1 gene mutation in twins by DHARNIDHARKA, Vikas R, RUTESHOUSER, E. Cristy, ROSEN, Seymour, KOZAKEWICH, Harry, HARRIS, H. William, HERRIN, John T, HUFF, Vicki

“…While a genetic basis for the association of developmental lung and kidney defects has been suspected, the involvement of specific genes in this process is…”
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Complications of pediatric percutaneous renal procedures: incidence and observations by Pfister, R C, Newhouse, J H, Yoder, I C, Hendren, W H, Kim, S H, Donahoe, P K, Herrin, J T

“…Successful definitive (complete) percutaneous renal procedures in the pediatric age group were performed in 97 per cent of antegrade pyelograms, in 94 per cent…”
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Pediatric renal transplantation by Herrin, John T.

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Peritoneal dialysis in the reduction of blood ammonia levels in a case of hyperammonaemia by 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 by Shannon, D C, De Long, R, Bercu, B, Glick, T, Herrin, J T, Moylan, F M, Todres, I D

“…The initial acid-base status of eight survivors of Reye's syndrome was characterized by acute respiratory alkalosis (Pco2=32 mm Hg; Hco3-=22.0 mEq/liter) while…”
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Ketamine induction in poor-risk patients by Nettles, D C, Herrin, T J, Mullen, J G

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