Mutations in the Glucose-6-Phosphatase Gene That Cause Glycogen Storage Disease Type 1a von Lei, Ke-Jian, Shelly, Leslie L., Pan, Chi-Jiunn, Sidbury, James B., Chou, Janice Yang

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Determination of fractional absorption of dietary calcium in humans von Yergey, A L, Abrams, S A, Vieira, N E, Aldroubi, A, Marini, J, Sidbury, J B

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Cornstarch Therapy in Type I Glycogen-Storage Disease von Chen, Yuan-Tsong, Cornblath, Marvin, Sidbury, James B

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Renal Disease in Type I Glycogen Storage Disease von Chen, Yuan-Tsong, Coleman, Rosalind A, Scheinman, JON I, Kolbeck, Peter C, Sidbury, James B

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Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c von Lei, K J, Shelly, L L, Lin, B, Sidbury, J B, Chen, Y T, Nordlie, R C, Chou, J Y

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Calcium kinetics in glycogen storage disease type 1a von Goans, R E, Weiss, G H, Vieira, N E, Sidbury, J B, Abrams, S A, Yergey, A L

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Stable isotope dilution thermospray liquid chromatography/mass spectrometry method for determination of sugars and sugar alcohols in humans von Esteban, Nora V, Liberato, Daniel J, Sidbury, James B, Yergey, Alfred L

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Type I glycogen storage disease: nine years of management with cornstarch von Chen, Y T, Bazzarre, C H, Lee, M M, Sidbury, J B, Coleman, R A

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Enzymatic alterations in Reye's syndrome: prognostic implications von Roe, C R, Schonberger, L B, Gelbach, S H, Wies, L A, Sidbury, Jr, J B

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Some inferences from galactokinase deficiency von Sidbury, Jr, J B

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Stimulation of hepatic fatty acid synthetase activity in chick embryo by cycloheximide von Joshi, V.C., Sidbury, J.B.

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Hormonal regulation of fatty acid synthetase in chick embryo liver von Joshi, V.C., Sidbury, J.B.

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Fatty acid synthesis in chick embryonic heart and liver during development von Joshi, V.C., Sidbury, J.B.

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Structure of calf lens β-crystallins von Samuel Zigler, J., Sidbury, J.B.

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An inborn error of short-chain fatty acid metabolism. The odor-of-sweaty-feet syndrome von Sidbury, Jr, J B, Smith, E K, Harlan, W

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Age-related changes in the free amino acid pool of rat lens von Zigler, JS, Jr, Mauney, ME, Sidbury, JB, Jr

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Hereditary alterations in the immune response: coexistence of "agammaglobulinemia", acquired hypogammaglobulinemia and selective immunoglobulin deficiency in a sibship von Buckley, R H, Sidbury, Jr, J B

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A New Dominant Progressive Foveal Dystrophy von Frank, H. Randolph, Iii, Maurice B. Landers, Williams, Randal J., Sidbury, J.B.

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A survey of genetics as it applies to problems in medicine von CHILDS, B, SIDBURY, Jr, J B

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Studies on beta-crystallin from primate lens von Zigler, JS, Jr, Sidbury, JB, Jr

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