Effect of glutamine synthetase inhibition on astrocyte swelling and altered astroglial protein expression during hyperammonemia in rats von Tanigami, H., Rebel, A., Martin, L.J., Chen, T.-Y., Brusilow, S.W., Traystman, R.J., Koehler, R.C.

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Inhibition of glutamine synthetase reduces ammonia-induced astrocyte swelling in rat von Willard-Mack, C.L., Koehler, R.C., Hirata, T., Cork, L.C., Takahashi, H., Traystman, R.J., Brusilow, S.W.

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Oral Sodium Phenylbutyrate Therapy in Homozygous β Thalassemia: A Clinical Trial von Collins, Anne F., Pearson, Howard A., Giardina, Patricia, McDonagh, Kevin T., Brusilow, Saul W., Dover, George J.

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Long-Term Treatment of Girls with Ornithine Transcarbamylase Deficiency von Maestri, Nancy E, Brusilow, Saul W, Clissold, David B, Bassett, Susan S

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Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis von Maestri, Nancy E., Clissold, David, Brusilow, Saul W.

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Urea cycle disorders : Diagnosis, pathophysiology, and therapy von BRUSILOW, S. W, MAESTRI, N. E

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Inhibition of brain glutamine accumulation prevents cerebral edema in hyperammonemic rats von Takahashi, H, Koehler, R. C, Brusilow, S. W, Traystman, R. J

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Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemia von Praphanproj, V., Boyadjiev, S. A., Waber, L. J., Brusilow, S. W., Geraghty, M. T.

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Phenylacetylglutamine may replace urea as a vehicle for waste nitrogen excretion von BRUSILOW, S. W

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Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus: A Cause of Postpartum Coma von Arn, Pamela Hawks, Hauser, Elizabeth R, Thomas, George H, Herman, Gail, Hess, David, Brusilow, Saul W

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In vivo evidence for the role of the epsilon subunit as an inhibitor of the proton-translocating ATPase of Escherichia coli von KLIONSKY, D. J, BRUSILOW, W. S. A, SIMONI, R. D

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Allopurinol-Induced Orotidinuria: A Test for Mutations at the Ornithine Carbamoyltransferase Locus in Women von Hauser, Elizabeth R, Finkelstein, Janice E, Valle, David, Brusilow, Saul W

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Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis von BRUSILOW, S. W

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Organization and Sequence of the Genes Coding for the Proton-translocating ATPase of Bacillus megaterium von Brusilow, W S A, Scarpetta, M A, Hawthorne, C A, Clark, W P

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Late-onset ornithine transcarbamylase deficiency in male patients von Finkelstein, J.E., Hauser, E.R., Leonard, C.O., Brusilow, S.W.

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Role of the delta subunit in enhancing proton conduction through the F0 of the Escherichia coli F1F0 ATPase von MONTICELLO, R. A, BRUSILOW, W. S. A

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Plasma glutamine concentration: A guide in the management of urea cycle disorders von Maestri, Nancy E., McGowan, Kathryn D., Brusilow, Saul W.

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Restoration of nitrogen homeostasis in a man with ornithine transcarbamylase deficiency von Brusilow, Saul W., Finkelstien, Janice

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RESTORATION OF CEREBROVASCULAR CO2 RESPONSIVITY BY GLUTAMINE SYNTHESIS INHIBITION IN HYPERAMMONEMIC RATS von TAKAHASHI, H, KOEHLER, RC, HIRATA, T, BRUSILOW, SW, TRAYSTMAN, RJ

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Proton leakiness caused by cloned genes for the F0 sector of the proton-translocating ATPase of Escherichia coli: requirement for F1 genes von BRUSILOW, W. S. A

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