Genetic PrP Prion Diseases

Cites (216)

Items 201–215 of 215

1. Atypical parkinsonism caused by Pro105Leu mutation of prion protein
   Kagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, Hiroyuki Ishiura, Shin‐ichi Tokushige, Yuji Takahashi, Naoko Saito Sato, Fumiko Kusunoki Nakamoto, Yaeko Ichikawa, Yu Nagashima et al. · 2016 · Neurology Genetics
2. A new point mutation of the PRNP gene in Gerstmann-Sträussler-Scheinker case in Poland.
   Jolanta Bratosiewicz, Maria Barcikowska, Larisa Červen̆áková, P Brown, Daniel Carleton Gajdusek, P P Liberski · 2000 · PubMed
3. A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings
   Claudio Mauro, Giorgio Giaccone, Giuseppe Piscosquito, Alfonso Lavorgna, M. Nigro, Giuseppe Di Fede, Antonio Leonardi, Cinzia Coppola, Silvestro Formisano, Fabrizio Tagliavini et al. · 2008 · Journal of Neurology Neurosurgery & Psychiatry
4. Multiparameter MR Imaging in the6-OPRIVariant of Inherited Prion Disease
   Enrico De Vita, Gerard R. Ridgway, Rachael I. Scahill, Diana Caine, Peter Rudge, Tarek Ahmed Yousry, Simon Mead, John Collinge, Hans Rolf Jäger, John S. Thornton et al. · 2013 · American Journal of Neuroradiology
5. R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease
   Maria Gabriella Vita, Simona Gaudino, Daniela Di Giuda, Donato Sauchelli, Paolo Emilio Alboini, Emma Gangemi, Alessandra Bizzarro, Eugenia Scaricamazza, Sabina Capellari, Piero Parchi et al. · 2013 · Journal of Neurology
6. A Patient With Creutzfeldt-Jakob Disease With an Insertion of 7 Octa-Repeats in the PRNP Gene: Molecular Characteristics and Clinical Features
   Yan-Jun Guo, Xiao‐Fan Wang, Jun Han, Baoyun Zhang, Qi Shi, Yan-Zhen Wan, Chen Gao, Xiao‐Ping Dong, Weiqin Zhao, Jimei Li et al. · 2008 · The American Journal of the Medical Sciences
7. De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia
   Milena Cannella, T. Martino, M Simonelli, Andrea Ciammola, Roberto Gradini, Andrea Ciarmiello, Fernando Gianfrancesco, Ferdinando Squitieri · 2007 · Journal of Neurology Neurosurgery & Psychiatry
8. [Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)].
   Jun Tateishi · 1991 · PubMed
9. Inherited prion disease with 4-octapeptide repeat insertion linked to valine at codon 129
   Raquel Sánchez‐Valle, Jordi Yagüe, Antoni Turon Estrada, Juan I. Aróstegui, Carlos Nos, Maria Jesus Rey, Isidró Ferrer, Ellen Gelpí · 2012 · Brain
10. Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation
    Atsushi Shiraishi, Hidehiro Mizusawa, Masahito Yamada · 2002 · Journal of Neurology
11. Molecular Genetics of Creutzfeldt–Jakob Disease and Gerstmann– Sträussler– Scheinker Disease
    Ellen Gelpí, Martí Colom‐Cadena, Herbert Budka · 2015 · Encyclopedia of Life Sciences
12. Axonal loss in multiple sclerosis lesions: magnetic resonance imaging insights substrates of disability
    Sperfeld · 1999 · Pure Amsterdam UMC
13. MEDICO -CHIRURGICAL SOCIETY, AND "THE LANCET."
    1824 · The Lancet
14. Untitled work
    Khan · 2000 · 10.1002/1531-8249(200008)48:2
15. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
    Parchi, Piero, Giese, Armin, Capellari, Sabina, Brown, Paul, Schulz-Schaeffer, Walter, Windl, Otto, Zerr, Inga, Budka, Herbert, Kopp, Nicolas, Piccardo, Pedro et al. · 1999 · Annals of Neurology