Segmental Renal Artery Embolization for Treatment of Pediatric Renovascular Hypertension von Teigen, Corey L., Mitchell, Sally E., Venbrux, Anthony C., Christenson, Marie J., McLean, Robert H.

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Hypoproteinemia in the hemolytic-uremic syndrome of childhood von Serebruany, V L, Christenson, M J, Pescetti, J, McLean, R H

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Thin Layer Isoelectric Focusing for Final Purification of Human C3 von McLean, Robert H

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Clinical expression of systemic lupus erythematosus in patients with C4A deficiency von Petri, M, Watson, R, Winkelstein, J A, McLean, R H

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Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndrome von McLean, Robert H., Chapitis, Jane, Weinstein, Arthur, Lowenstein, Mitchell, Rothfield, Naomi F.

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Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and Black Americans von Howard, Paul F., Hochberg, Marc C., Bias, Wilma B., Arnett, Frank C., McLean, Robert H.

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Multinodular hemangiomatosis of the liver in infancy von McLean, R H, Moller, J H, Warwick, W J, Satran, L, Lucas, Jr, R V

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Preservation of C3, C5, and C5a Functional Activities by a New Radiolabeling Method; Demonstration of C5 Products in Complement-Activated Serum von Kreutzer, Donald L, Kunkel, Steven, Ward, Peter A, Showell, Henry, McLean, Robert H

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Neonatal hemodialysis: Effective therapy for the encephalopathy of inborn errors of metabolism von Rutledge, S. Lane, Havens, Peter L., Haymond, Morey W., McLean, Robert H., Kan, Jean S., Brusilow, Saul W.

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Association of Homozygous C4B Deficiency with Bacterial Meningitis von Rowe, Peter C., McLean, Robert H., Wood, Robert A., Leggiadro, Robert J., Winkelstein, Jerry A.

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Complement and glomerulonephritis : an update von MCLEAN, R. H

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Hypoplasia of the rightventricle and tricuspid valve in siblings von Davachi, Farzin, McLean, Robert H., Moller, James H., Edwards, Jesse E.

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Complement phenotypes in glomerulonephritis: Increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura von McLean, Robert H., Wyatt, Robert J., Julian, Bruce A.

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Hemolytically inactive C4B complement allotype caused by a proline to leucine mutation in the C5-binding site von McLean, R H, Niblack, G, Julian, B, Wang, T, Wyatt, R, Phillips, J A, Collins, T S, Winkelstein, J, Valle, D

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Neonatal Lupus Erythematosus Syndrome: Analysis of C4 Allotypes and C4 Genes in 18 Failies von Watson, Rosemarie M., Scheel, Janet N., Petri, Michelle, Lee, Lela A., Bias, Wilma B., McLean, Robert H.

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Association of Henoch-Schönlein purpura glomerulonephritis with C4B deficiency von Ault, Bettina H., Stapleton, F. Bruder, Rivas, Marian L., Waldo, F. Bryson, Roy, Shane, McLean, Robert H., Bin, Jiang, Wyatt, Robert J.

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Familial deficiency of C5 in humans: Intact but deficient alternative complement pathway activity von McLean, Robert H., Peter, Georges, Gold, Ronald, Guerra, Levi, Yunis, Edmund J., Kreutzer, Donald L.

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A unique recombination event resulting in a C4AQ0,C4BQ0 double null haplotype von FASANO, M. B, WINKELSTEIN, J. A, LAROSA, T, BIAS, W. B, MCLEAN, R. H

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Central nervous system involvement in hemolytic-uremic syndrome von Markel, Howard, McLean, Robert H.

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Prevalence of polymorphic 21-hydroxylase gene (Ca21HB) mutations in salt-losing congenital adrenal hyperplasia von Jospe, Nicholas, Donohoue, Patricia A., Van Dop, Cornelis, McLean, Robert H., Bias, Wilma B., Migeon, Claude J.

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