Distribution of Neisseria meningitidis serogroup B serosubtypes and serotypes circulating in the United States von TONDELLA, M. L. C, POPOVIC, T, ROSENSTEIN, N. E, LAKE, D. B, CARLONE, G. M, MAYER, L. W, PERKINS, B. A

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Loci for Classical and a Variant Late Infantile Neuronal Ceroid Lipofuscinosis Map to Chromosomes 11p15 and 15q21–23 von Sharp, J. D., Wheeler, R. B., Lake, B. D., Savukoski, M., Järvelä, I. E., Peltonen, L., Gardiner, R. M., Williams, R. E.

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Deficiency of respiratory chain complex I is a common cause of leigh disease von Morris, A. A. M., Leonard, J. V., Brown, G. K., Bidouki, S. K., Bindoff, L. A., Turnbull, D. M., Woodward, C. E., Harding, A. E., Lake, B. D., Harding, B. N., Farrell, M. A., Bell, J. E., Mirakhur, M.

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A Missense Mutation of Cytochrome Oxidase Subunit II Causes Defective Assembly and Myopathy von Rahman, Shamima, Taanman, Jan-Willem, Cooper, J. Mark, Nelson, Isabelle, Hargreaves, Ian, Meunier, Brigitte, Hanna, Michael G, García, José J., Capaldi, Roderick A., Lake, Brian D., Leonard, James V., Schapira, Anthony H.V.

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Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1 von MCGRATH, J. A, HOEGER, P. H, EADY, R. A. J, CHRISTIANO, A. M, MCMILLAN, J. R, MELLERIO, J. E, ASHTON, G. H. S, DOPPING-HEPENSTAL, P. J. C, LAKE, B. D, LEIGH, I. M, HARPER, J. I

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Mutations in the Palmitoyl-Protein Thioesterase Gene (PPT; CLN1) Causing Juvenile Neuronal Ceroid Lipofuscinosis with Granular Osmiophilic Deposits von Mitchison, Hannah M., Hofmann, Sandra L., Becerra, Carlos H. R., Munroe, Patricia B., Lake, Brian D., Crow, Yanick J., Stephenson, John B. P., Williams, Ruth E., Hofman, Irene L., Taschner, Peter E. M., Martin, Jean-Jacques, Philippart, Michel, Andermann, Eva, Andermann, Frederick, Mole, Sara E., Gardiner, R. Mark, O'Rawe, Angela M.

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Tacrolimus von Lake, D B, Poole, T R G

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A new point mutation associated with mitochondrial encephalomyopathy von Morten, K.J., Cooper, J.M., Brown, G.K., Lake, B.D., PIke, D., Poulton, J.

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Liver failure associated with mitochondrial DNA depletion von Morris, Andrew A.M., Taanman, Jan-Willem, Blake, Julian, Mark Cooper, J., Lake, Brian D., Malone, Marion, Love, Seth, Clayton, Peter T., Leonard, James V., Schapira, Anthony H.V.

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Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis) von HALL, N. A, LAKE, B. D, DEWJI, N. N, PATRICK, A. D

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Niemann-Pick disease type C: Diagnosis and outcome in children, with particular reference to liver disease von Kelly, Deirdre A., Portmann, Bernard, Mowat, Alex P., Sherlock, Sheila, Lake, Brian D.

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Management of skin retraction associated with Boston type II keratoprosthesis von Nanavaty, M A, Avisar, I, Lake, D B, Daya, S M, Malhotra, R

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Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease) von Bronson, Roderick T., Lake, Brian D., Cook, Susan, Taylor, Susanne, Davisson, Muriel T.

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Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease) von Palmer, David N., Fearnley, Ian M., Walker, John E., Hall, Nicholas A., Lake, Brian D., Wolfe, Leonhard S., Haltia, Matti, Martinus, Ryan D., Jolly, Robert D.

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Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms von Rahman, Shamima, Lake, Brian D., Taanman, Jan-Willem, Hanna, Michael G., Cooper, J. Mark, Schapira, Anthony H. V., Leonard, James V.

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Infantile systemic hyalinosis : newly recognized disorder of collagen ? von GLOVER, M. T, LAKE, B. D, ATHERTON, D. J

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Intestinal neuronal dysplasia. Why does it only occur in parts of Europe? von Lake, B D

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A New Locus for Variant Late Infantile Neuronal Ceroid Lipofuscinosis—CLN7 von Wheeler, R.B, Sharp, J.D, Mitchell, W.A, Bate, S.L, Williams, R.E, Lake, B.D, Gardiner, R.M

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Lymphocyte Inclusions in Finnish-Variant Late Infantile Neuronal Ceroid Lipofuscinosis (CLN5) von Rapola, J., Lake, B. D.

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Bone Marrow Transplantation in Late Infantile Batten Disease and Juvenile Batten Disease von Lake, B. D., Steward, C. G., Oakhill, A., Wilson, J., Perham, T. C.

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