A novel sodium channel mutation in a family with hypokalemic periodic paralysis von BULMAN, D. E, SCOGGAN, K. A, VAN OENE, M. D, NICOLLE, M. W, HAHN, A. F, TOLLAR, L. L, EBERS, G. C

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The Human Skeletal Muscle Na Channel Mutation R669H Associated with Hypokalemic Periodic Paralysis Enhances Slow Inactivation von Struyk, Arie F, Scoggan, Kylie A, Bulman, Dennis E, Cannon, Stephen C

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Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2 von SCOGGAN, K A, CHANDRA, T, NELSON, R, HAHN, A F, BULMAN, D E

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Differential Activation of Leukotriene Biosynthesis by Granulocyte-Macrophage Colony-Stimulating Factor and Interleukin-5 in an Eosinophilic Substrain of HL-60 Cells von Scoggan, Kylie A., Ford-Hutchinson, Anthony W., Nicholson, Donald W.

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Photoaffinity labelling and radiation inactivation of the leukotriene B4 receptor in human myeloid cells von SLIPETZ, D. M, SCOGGAN, K. A, NICHOLSON, D. W, METTERS, K. M

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A missense mutation in the Abcg5 gene causes phytosterolemia in SHR, stroke-prone SHR, and WKY rats von Scoggan, Kylie A, Gruber, Heidi, Lariviere, Katherine

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Production of Leukotriene C4 in Different Human Tissues Is Attributable to Distinct Membrane Bound Biosynthetic Enzymes von Scoggan, K A, Jakobsson, P J, Ford-Hutchinson, A W

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Regulation of Leukotriene‐Biosynthetic Enzymes During Differentiation of Myelocytic HL‐60 Cells to Eosinophilic or Neutrophilic Cells von Scoggan, Kylie A., Nicholson, Donald W., Ford‐Hutchinson, Anthony W.

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Characterization of microsomal GST-II by western blot and identification of a novel LTC4 isomer von Jakobsson, P J, Scoggan, K A, Yergey, J, Mancini, J A, Ford-Hutchinson, A W

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Large French-Canadian family with Lewy body parkinsonism: Exclusion of known loci von Grimes, David A., Grimes, J. David, Racacho, Lem, Scoggan, Kylie A., Han, Fabin, Schwarz, Betty Anne, Woulfe, John, Bulman, Dennise

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Identification of two novel mutations in the CACNA1A gene responsible for episodic ataxia type 2 von Scoggan, K A, Chandra, T, Nelson, R, Hahn, A F, Bulman, D E

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