Molecular neurology of prion disease

od Collinge, J
Izdano 2005

Reported management of threatened miscarriage by general practitioners in Wessex.

od Collinge, J D
Izdano 1987

Points: Gastroenterology services in Trent

od Collinge, J Deane
Izdano 1984

Patient package inserts.

od Collinge, J D
Izdano 1978

Dispensing in general practice: Short term prescribing not driven by money

od Collinge, J Deane
Izdano 1993

The molecular pathology of CJD: old and new variants

od Jackson, G S, Collinge, J
Izdano 2001

The molecular biology of prion propagation.

od Clarke, A R, Jackson, G S, Collinge, J
Izdano 2001

Codon 129 changes in the prion protein gene in Caucasians.

od Owen, F, Poulter, M, Collinge, J, Crow, T J
Izdano 1990

Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease

od Joiner, S, Linehan, J, Brandner, S, Wadsworth, J, Collinge, J
Izdano 2002

Studies on the interaction between cerebral 5-hydroxytryptamine and gamma-aminobutyric acid in the mode of action of diazepam in the rat.

od Collinge, J., Pycock, C. J., Taberner, P. V.
Izdano 1983

Review: Contribution of transgenic models to understanding human prion disease

od Wadsworth, J D F, Asante, E A, Collinge, J
Izdano 2010

Maturation of caffeine elimination in infancy.

od Aranda, J V, Collinge, J M, Zinman, R, Watters, G
Izdano 1979

Cultural factors that affected the spatial and temporal epidemiology of kuru

od Whitfield, J. T., Pako, W. H., Collinge, J., Alpers, M. P.
izdano v R Soc Open Sci (2017)

High levels of disease related prion protein in the ileum in variant Creutzfeldt-Jakob disease

od Joiner, S, Linehan, J M, Brandner, S, Wadsworth, J D F, Collinge, J
Izdano 2005

Inherited prion disease (PrP lysine 200) in Britain: two case reports.

od Collinge, J, Palmer, M S, Campbell, T, Sidle, K C, Carroll, D, Harding, A
Izdano 1993

Transmission of scrapie by steel-surface-bound prions.

od Flechsig, E., Hegyi, I., Enari, M., Schwarz, P., Collinge, J., Weissmann, C.
Izdano 2001

Neuroimaging findings in human prion disease

od Macfarlane, R G, Wroe, S J, Collinge, J, Yousry, T A, Jäger, H R
Izdano 2007

Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases

od Isaacs, A M, Powell, C, Webb, T E, Linehan, J M, Collinge, J, Brandner, S
Izdano 2008

The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease

od Cordery, R, Alner, K, Cipolotti, L, Ron, M, Kennedy, A, Collinge, J, Rossor, M
Izdano 2005

Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.

od Collinge, J, Poulter, M, Davis, M B, Baraitser, M, Owen, F, Crow, T J, Harding, A E
Izdano 1991