A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe von Abbas, Nacer, Lücking, Christoph B., Ricard, Sylvain, Dürr, Alexandra, Bonifati, Vincenzo, De Michele, Giuseppe, Bouley, Sandrine, Vaughan, Jenny R., Gasser, Thomas, Marconi, Roberto, Broussolle, Emmanuel, Brefel-Courbon, Christine, Harhangi, Biswadjiet S., Oostra, Ben A., Fabrizio, Edito, Böhme, Georg A., Pradier, Laurent, Wood, Nick W., Filla, Alessandro, Meco, Giuseppe, Denefle, Patrice, Agid, Yves, Brice, Alexis

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Disease Risk Analysis and Post‐Release Health Surveillance for a Reintroduction Programme: the Pool Frog Pelophylax lessonae von Sainsbury, A. W., Yu‐Mei, R., Ågren, E., Vaughan‐Higgins, R. J., Mcgill, I. S., Molenaar, F., Peniche, G., Foster, J.

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Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease von Martinez, M, Brice, A, Vaughan, J R, Zimprich, A, Breteler, M M B, Meco, G, Filla, A, Farrer, M J, Bétard, C, Hardy, J, De Michele, G, Bonifati, V, Oostra, B, Gasser, T, Wood, N W, Dürr, A

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Multiple system atrophy/progressive supranuclear palsy : α-synuclein, synphilin, tau, and APOE von MORRIS, H. R, VAUGHAN, J. R, DANIEL, S, LEES, A. J, QUINN, N. P, WOOD, N. W, DATTA, S. R, BANDOPADHYAY, R, ROHAN DE SILVA, H. A, SCHRAG, A, CAIRNS, N. J, BURN, D, NATH, U, LANTOS, P. L

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Genetics of Parkinsonism: a review von VAUGHAN, J. R., DAVIS, M. B., WOOD, N. W.

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CRYPTOCOCCOSIS IN GILBERT'S AND LONG-NOSED POTOROO von Vaughan, R. J, Vitali, S. D, Eden, P. A, Payne, K. L, Warren, K. S, Forshaw, D, Friend, J. A, Horwitz, A. M, Main, C, Krockenberger, M. B, Malik, R

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Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study von NICHOLL, D. J, VAUGHAN, J. R, DANIEL, S. E, LENNOX, G. G, BROOKS, D. J, WILLIAMS, A. C, WOOD, N. W, KHAN, N. L, HO, S. L, ALDOUS, D. E. W, LINCOLN, S, FARRER, M, GAYTON, J. D, DAVIS, M. B, PICCINI, P

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Biosecurity for Translocations: Cirl Bunting (Emberiza cirlus), Fisher’s Estuarine Moth (Gortyna borelii lunata), Short-Haired Bumblebee (Bombus subterraneus) and Pool Frog (Peloph... von Vaughan-Higgins, R. J., Masters, N., Sainsbury, A. W.

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A new formula for secondary emission yield von Vaughan, J.R.M.

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Sequencing of the α-Synuclein Gene in a Large Series of Cases of Familial Parkinson's Disease Fails to Reveal any Further Mutations von Vaughan, Jenny R., Farrer, Matthew J., Wszolek, Zbigniew K., Gasser, Thomas, Durr, Alexandra, Agid, Yves, Bonifati, Vincenzo, DeMichele, Giuseppe, Volpe, Gianpiero, Lincoln, Sarah, Breteler, Monique, Meco, Giuseppe, Brice, Alexis, David Marsden, C., Hardy, John, Wood, Nicholas W.

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Cavum septum pellucidum and obstructive hydrocephalus von Silbert, P L, Gubbay, S S, Vaughan, R J

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Gross and histopathological findings in hindlimb paralysis syndrome in wild Carnaby's black cockatoos (Zanda laitirostris) von Coiacetto, Flaminia J., Rossi, Gabriele, Stephens, Nahiid, Vaughan-Higgins, Rebecca J.

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The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease von Harhangi, B.Sanjay, Farrer, Matthew J., Lincoln, Sarah, Bonifati, Vincenzo, Meco, Giuseppe, De Michele, Giuseppe, Brice, Alexis, Dürr, Alexandra, Martinez, Maria, Gasser, Thomas, Bereznai, Benjamin, Vaughan, Jenny R., Wood, Nicholas W., Hardy, John, Oostra, Ben A., Breteler, Monique M.B.

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Effect of Chronic Administration of Mestranol, Tamoxifen, and Toremifene on Hepatic Ploidy in Rats von Dragan, Y. P., Shimel, R. J., Bahunb, N., Sattler, G., Vaughan, J. R., Jordan, V. C., Pitot, H. C.

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Genetic complexity and Parkinson's disease von Gasser, T, Müller-Myhsok, B, Wszolek, Z K, Dürr, A, Vaughan, J R, Bonifati, V, Meco, G, Bereznai, B, Oehlmann, R, Agid, Y, Brice, A, Wood, N

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A critically co-endangered feather louse Forficuloecus pezopori n. sp. (Phthiraptera: Philopteridae) detected through conservation intervention for the western ground parrot Pezopo... von Martin, Storm Blas, Keatley, Sarah, Wallace, Alisa, Vaughan-Higgins, Rebecca J., Ash, Amanda

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Detailed genotyping demonstrates association between the slow acetylator genotype for N-Acetyltransferase 2 (NAT2) and familial parkinson's disease von Bandmann, Oliver, Vaughan, Jenny R., Holmans, Peter, Marsden, C. David, Wood, Nicholas W.

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Palisades in primary cerebral neuroblastoma simulating so-called polar spongioblastoma: a light and electron microscopical study of an adult case von OJEDA, V. J, SPAGNOLO, D. V, VAUGHAN, R. J

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An investigation of the auditory streaming effect using event-related brain potentials von SUSSMAN, ELYSE, RITTER, WALTER, VAUGHAN, HERBERT G.

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Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects von Periquet, Magali, Lücking, Christoph B., Vaughan, Jenny R., Bonifati, Vincenzo, Dürr, Alexandra, De Michele, Giuseppe, Horstink, Martin W., Farrer, Matt, Illarioshkin, Sergei N., Pollak, Pierre, Borg, Michel, Brefel-Courbon, Christine, Denefle, Patrice, Meco, Giuseppe, Gasser, Thomas, Breteler, Monique M.B., Wood, Nick W., Agid, Yves, Brice, Alexis

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