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	41.	Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation. [electronic resource] by Cochran, E J Bennett, D A Cervenáková, L Kenney, K Bernard, B Foster, N L Benson, D F Goldfarb, L G Brown, P Producer: 19961122 In: Neurology vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin. [electronic resource] by Goldfarb, L G Brown, P Haltia, M Cathala, F McCombie, W R Kovanen, J Cervenáková, L Goldin, L Nieto, A Godec, M S Producer: 19920825 In: Annals of neurology vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy. [electronic resource] by Brown, P Kenney, K Little, B Ironside, J Will, R Cervenáková, L Bjork, R J San Martin, R A Safar, J Roos, R Producer: 19950922 In: Annals of neurology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation. [electronic resource] by Chapman, J Arlazoroff, A Goldfarb, L G Cervenakova, L Neufeld, M Y Werber, E Herbert, M Brown, P Gajdusek, D C Korczyn, A D Producer: 19960613 In: Neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Molecular genetic testing of a fetus at risk of Gerstmann-Sträussler-Scheinker syndrome. [electronic resource] by Brown, P Cervenáková, L Goldfarb, L G Gajdusek, D C Haverkamp, A Haverkamp, C Horwitz, J Creacy, S D Bever, R A Wexler, P Producer: 19940210 In: Lancet (London, England) vol. 343 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine. [electronic resource] by Brown, P Cervenáková, L Goldfarb, L G McCombie, W R Rubenstein, R Will, R G Pocchiari, M Martinez-Lage, J F Scalici, C Masullo, C Producer: 19940317 In: Neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. [electronic resource] by Goldfarb, L G Brown, P McCombie, W R Goldgaber, D Swergold, G D Wills, P R Cervenakova, L Baron, H Gibbs, C J Gajdusek, D C Producer: 19920109 In: Proceedings of the National Academy of Sciences of the United States of America vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Missense mutations in desmin associated with familial cardiac and skeletal myopathy. [electronic resource] by Goldfarb, L G Park, K Y Cervenáková, L Gorokhova, S Lee, H S Vasconcelos, O Nagle, J W Semino-Mora, C Sivakumar, K Dalakas, M C Producer: 19980901 In: Nature genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Clinical and genetic studies of fatal familial insomnia. [electronic resource] by Reder, A T Mednick, A S Brown, P Spire, J P Van Cauter, E Wollmann, R L Cervenàkovà, L Goldfarb, L G Garay, A Ovsiew, F Producer: 19950718 In: Neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies. [electronic resource] by Chapman, J Cervenáková, L Petersen, R B Lee, H S Estupinan, J Richardson, S Vnencak-Jones, C L Gajdusek, D C Korczyn, A D Brown, P Goldfarb, L G Producer: 19980908 In: Neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS). [electronic resource] by Cervenakova, L Protas, I I Hirano, A Votiakov, V I Nedzved, M K Kolomiets, N D Taller, I Park, K Y Sambuughin, N Gajdusek, D C Brown, P Goldfarb, L G Producer: 20001023 In: Journal of the neurological sciences vol. 177 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Iatrogenic Creutzfeldt-Jakob disease at the millennium. [electronic resource] by Brown, P Preece, M Brandel, J P Sato, T McShane, L Zerr, I Fletcher, A Will, R G Pocchiari, M Cashman, N R d'Aignaux, J H Cervenáková, L Fradkin, J Schonberger, L B Collins, S J Producer: 20001207 In: Neurology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease. [electronic resource] by Lee, H S Sambuughin, N Cervenakova, L Chapman, J Pocchiari, M Litvak, S Qi, H Y Budka, H del Ser, T Furukawa, H Brown, P Gajdusek, D C Long, J C Korczyn, A D Goldfarb, L G Producer: 20000405 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)