ADVF - Esteban,J.C.; Atares,B.; Zarranz,J.J.; Velasco,F.; Lambarri,I. - Dementia, amyotrophy, and periodic complexes on the electroencephalogram: a diagnostic challenge. - Archives of Neurology 2001 Oct; 58(10): 1669-72
ATVG - Zarranz,J.J.; Digon,A.; Atares,B.; Rodriguez-Martinez,A.B.; Arce,A.; Carrera,N.; Fernandez-Manchola,I.; Fernandez-Martinez,M.; Fernandez-Maiztegui,C.; Forcadas,I.; Galdos,L.; Gomez-Esteban,J.C.; Ibanez,A.; Lezcano,E.; Lopez de Munain,A.; Marti-Masso,J.F.; Mendibe,M.M.; Urtasun,M.; Uterga,J.M.; Saracibar,N.; Velasco,F.; de Pancorbo,M.M. - Phenotypic variability in familial prion diseases due to the D178N mutation - Journal of Neurology, Neurosurgery and Psychiatry 2005 Nov; 76(11): 1491-6
ARLH - Zarranz,J.J.; Digon,A.; Atares,B.; Arteagoitia,J.M.; Carrera,N.; Fernandez-Manchola,I.; Fernandez-Martinez,M.; Fernandez-Maiztegui,C.; Forcadas,I.; Galdos,L.; Ibanez,A.; Lezcano,E.; Marti-Masso,J.F.; Mendibe,M.M.; Urtasun,M.; Uterga,J.M.; Saracibar,N.; Velasco,F.; Gonzalez de Galdeano,L. - Familial prion diseases in the Basque Country (Spain) - Neuroepidemiology 2005; 24(1-2): 103-9
AUTP - Coimbra,E.R.; Rezek,K.; Escorsi-Rosset,S.; Landemberger,M.C.; Castro,R.M.R.P.S.; Valadao,M.N.; Guarnieri,R.; Velasco,T.R.; Terra-Bustamante,V.C.; Bianchin,M.M.; Wichert-Ana,L.; Alexandre,V.Jr.; Brentani,R.R.; Martins,V.R.; Sakamoto,A.C.; Walz,R. - Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171 - Epilepsy & Behavior 2006 May; 8(3): 635-42
ARUH - Walz,R.; Castro,R.M.R.P.S.; Landemberger,M.C.; Velasco,T.R.; Terra-Bustamante,V.C.; Bastos,A.C.; Bianchin,M.M.; Wichert-Ana,L.; Araujo,D.; Alexandre,V.Jr.; Santos,A.C.; Machado,H.R.; Carlotti,C.G.Jr.; Brentani,R.R.; Martins,V.R.; Sakamoto,A.C. - Cortical malformations are associated with a rare polymorphism of cellular prion protein - Neurology 2004 Aug 10; 63(3): 557-60
APNA - Walz,R.; Castro,R.M.R.P.S.; Velasco,T.R.; Alexandre,V.Jr.; Lopes,M.H.; Leite,J.P.; Santos,A.C.; Assirati,J.A.Jr.; Wichert-Ana,L.; Terra-Bustamante,V.C.; Bianchin,M.M.; Maciag,P.C.; Ribeiro,K.B.; Guarnieri,R.; Araujo,D.; Caballero,O.L.; Moura,R.; Salim,A.C.; Kindlmann,K.; Landemberger,M.C.; Marques,W.Jr.; Fernandes,R.M.; Serafini,L.N.; Machado,H.R.; Carlotti,C.G.Jr.; Brentani,R.R.; Sakamoto,A.C.; Martins,V.R. - Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variant - Neurology 2003 Nov 11; 61(9): 1204-10
AWVS - Walz,R.; Castro,R.M.R.P.S.; Velasco,T.R.; Alexandre,V.Jr.; Maciag,P.C.; Wichert-Ana,L.; Terra-Bustamante,V.C.; Leite,J.P.; Fernandes,R.M.; Marques,W.Jr.; Machado,H.R.; Carlotti,C.G.Jr.; Assirati,J.A.Jr.; Moura,R.; Caballero,O.L.; Sakamoto,A.C.; Brentani,R.R.; Martins,V.R. - Human cellular prion protein gene variant allels are associated with intractable symptomatic epilepsies - Epilepsia 2002 Oct; 43(Supplement 7): 278, Abstract: 3.087
AMFA - Walz,R.; Castro,R.M.R.P.S.; Velasco,T.R.; Carlotti,C.G.Jr.; Sakamoto,A.C.; Brentani,R.R.; Martins,V.R. - Cellular prion protein: implications in seizures and epilepsy. - Cellular and Molecular Neurobiology 2002 Jun; 22(3): 249-57