Apoe ϵ2-ϵ4 genotype is a possible risk factor for primary progressive aphasia
Adele Acciarri MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorCarlo Masullo MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAlessandra Bizzarro MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAlessandro Valenza MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorDavide Quaranta MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorCamillo Marra MD, PhD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorFrancesco D. Tiziano MD
Institute of Medical Genetics, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorChristina Brahe PhD
Institute of Medical Genetics, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorDavide Seripa PhD
Pathology of Aging Research Unit, I.R.C.C.S. “Casa Sollievo della Sofferenza,” S. Giovanni Rotondo, FG, Italy
Search for more papers by this authorMaria G. Matera PhD
Pathology of Aging Research Unit, I.R.C.C.S. “Casa Sollievo della Sofferenza,” S. Giovanni Rotondo, FG, Italy
Search for more papers by this authorVito M. Fazio MD
Laboratory of Molecular Medicine and Biotechnology, Campus Bio-Medico University School of Medicine, Rome, Italy
Search for more papers by this authorGuido Gainotti MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAntonio Daniele MD, PhD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAdele Acciarri MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorCarlo Masullo MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAlessandra Bizzarro MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAlessandro Valenza MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorDavide Quaranta MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorCamillo Marra MD, PhD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorFrancesco D. Tiziano MD
Institute of Medical Genetics, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorChristina Brahe PhD
Institute of Medical Genetics, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorDavide Seripa PhD
Pathology of Aging Research Unit, I.R.C.C.S. “Casa Sollievo della Sofferenza,” S. Giovanni Rotondo, FG, Italy
Search for more papers by this authorMaria G. Matera PhD
Pathology of Aging Research Unit, I.R.C.C.S. “Casa Sollievo della Sofferenza,” S. Giovanni Rotondo, FG, Italy
Search for more papers by this authorVito M. Fazio MD
Laboratory of Molecular Medicine and Biotechnology, Campus Bio-Medico University School of Medicine, Rome, Italy
Search for more papers by this authorGuido Gainotti MD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this authorAntonio Daniele MD, PhD
Institute of Neurology, Catholic University School of Medicine, Rome, Italy
Search for more papers by this author
References
- 1 Masullo C, Daniele A, Fazio VM, et al. The apolipoprotein E genotype in patients affected by syndromes with focal cortical atrophy. Neurosci Lett 2001; 303: 87–90.
- 2 Verpillat P, Camuzat A, Hannequin D, et al. Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis. Eur J Hum Genet 2002; 10: 399–405.
- 3 McKhann GM, Albert MS, Grossman M, et al. Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease. Arch Neurol 2001; 58: 1803–1809.
- 4 Mesulam MM. Primary progressive aphasia. Ann Neurol 2001; 49: 425–432.
- 5 Comings DE, MacMurray JP. Molecular heterosis: a review. Mol Genet Metab 2000; 71: 19–31.