Parkinson disease and amyotrophic lateral sclerosis: Tauopathies, TDP-43 and SOD mutations;Syndromes parkinsoniens et sclérose latérale amyotrophique: Tauopathies, TDP-43 et mutations SOD

Revue Neurologique

Volumn 165, Issue 1, 2009, Pages 15-30

  Le Forestier, N ^a   Lacomblez, L ^a   Meininger, V ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TAR DNA BINDING PROTEIN; DNA BINDING PROTEIN; PROTEIN TDP-43; SUPEROXIDE DISMUTASE; TAU PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; CORTICOBASAL DEGENERATION; DEGENERATIVE DISEASE; DEMENTIA; DISEASE ASSOCIATION; HUMAN; MOTOR NEURON DISEASE; MOTOR SYSTEM; MUTATION; PARKINSON DISEASE; PROGRESSIVE SUPRANUCLEAR PALSY; PYRAMIDAL TRACT; REVIEW; TAUOPATHY; ANIMAL; EXTRAPYRAMIDAL SYNDROME; GENETICS; METABOLISM; PHYSIOLOGY;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; BASAL GANGLIA DISEASES; DNA-BINDING PROTEINS; HUMANS; MUTATION; PARKINSON DISEASE; SUPEROXIDE DISMUTASE; TAU PROTEINS;

EID: 62449283111     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neurol.2008.02.043     Document Type: Review

References (258)

1. H. Abalkhail, J. Mitchell, J. Habgood, R. Orrell, and J. De Belleroche A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2 Am J Hum Genet 73 2003 383 389
2. G. Abbruzzese, M. Tabaton, M. Morena, D. Dall'Agata, and E. Favale Motor and sensory evoked potentials in progressive supranuclear palsy Mov Disord 6 1991 49 54
3. S. Abrahams, P.N. Leigh, A. Harvey, G.N. Vythelingum, D. Grise, and L.H. Goldstein Verbal fluency and executive dysfunction in amyotrophic lateral sclerosis (ALS) Neuropsychologia 38 2000 734 747
4. S. Abrahams, P.N. Leigh, and L.H. Goldstein Cognitive changes in ALS: a prospective study Neurology 64 2005 339 350
5. I. Aiba, Y. Hashizume, M. Yoshida, S. Okuda, N. Murakami, and N. Ujihira Relationship between brainstem MRI and pathologic findings in progressive supranuclear palsy: study in autopsy cases J Neurol Sci 152 1997 210 217
6. K. Akai, R. Kawaguchi, K.K. Yamada, S. Uchigasaki, Y. Sawaguchi, and K. Yoshino Clinicopathologic study of a case with features of presenile dementia and motor neuron disease Neuropathology (Tokyo) 3 1982 39 48
7. A.J. Akelaitis Atrophy of basal ganglia in Pick's disease. A clinicopathologic study Arch Neurol Psychiatr 51 1944 27 34
8. D.S. Albers, S.J. Augood, D.M. Martin, D.G. Standaert, J.P. Vonsattel, and M.F. Beal Evidence for oxidative stress in the subthalamic nucleus in progressive supranuclear palsy J Neurochem 73 1999 881 884
9. D.S. Albers, and M.F. Beal Mitochondrial dysfunction and oxidative stress in aging and neurodegenerative disease J Neural Transm Suppl 59 2000 133 154
10. D.S. Albers, S.J. Augood, and L.C. Park Frontal lobe dysfunction in progressive supranuclear palsy: evidence for oxidative stress and mitochondrial impairment J Neurochem 74 2000 878 881
11. M. Alter, and B. Schaumann Hereditary amyotrophic lateral sclerosis. A report of two families Eur J Neurol 14 1976 250 263
12. P.M. Andersen, G.D. Borasio, and R. Dengler EFNS task force on management of amyotrophic lateral sclerosis: guidelines for diagnosis and clinical care of patients and relatives Eur J Neurol 12 2005 921 938
13. F.H. Anderson, E.P. Richardson Jr., H. Okazaki, and J.A. Brody Neurofibrillary degeneration on Guam. Frequency in chamorros and non-chamorros with no known neurological disease Brain 102 1979 65 77
14. A. Andreadis, W.M. Brown, and K.S. Kosik Structure and novel exons of the human tau gene Biochemistry 31 1992 10626 10633
15. K. Aoyama, K. Matsubra, and S. Kobayashi Aging and oxidative stress in progressive supranuclear palsy Eur J Neurol 13 2006 89 92
16. J. Avila Tau aggregation into fibrillar polymers: tauopathies FEBS Lett 476 2000 89 92
17. M. Azzouz, P. Poindron, and S. Guettier Prevention of mutant SOD1 motoneuron degeneration by copper chelator in vitro J Neurobiol 42 2000 49 55
18. M. Bergmann, K. Schmidtke, A. Danek, F. Gullota, and P. Mehraein Striato-nigral degeneration (SND): a multisystem atrophy? Schweiz Arch Neurol Psychiatr 141 1990 389 405
19. M. Bergmann, K. Kuchelmeister, A. Migheli, D. Schiffer, and F. Gullotta Motor neuron disease with pallido-luyso-nigral atrophy Acta Neuropathol (Berl) 86 1993 105 108
20. I. van Bertrand, and L. van Bogaert La sclérose latérale amyotrophique (anatomie pathologique) Rev Neurol 32 1923 779 806
21. A. Biemond, and W. Beck Neural Muscle Atrophy with degeneration of the substantia nigra Confin Neurol 15 1955 142 153
22. E.H. Bigio, A.M. Lipton, and S.H. Yen Frontal dementia with novel tauopathy: sporadic multiple system tauopathy with dementia J Neuropathol Exp Neurol 60 2001 328 341
23. T. Bird, D. Knopman, and J.B. van Swieten Epidemiology and genetics of frontotemporal dementia/Pick's disease Ann Neurol 54 Suppl. 5 2003 S29 S31
24. G.D. Borasio, R. Linke, and J. Schwarz Dopaminergic deficit in amyotrophic lateral sclerosis assessed with [I-123] IPT single photon emission computed tomography J Neurol Neurosurg Psychiatry 65 1998 263 265
25. J. Boudouresques, M. Toga, R. Khalil, A. Ali Cherif, J.F. Pelissier, and A. Gosset Dégénérescence spino-cérébelleuse tardive avec amyotrophie comportant une atteinte pallido-luysienne sévre et des lésions histologiques diffuses de sénilité (étude anatomo-clinique d'un cas avec discussion nosographique) Rev Neurol 132 1976 623 638
26. S. Brion, A. Psimaras, J.F. Chevalier, J. Plas, G. Masse, and O. Jatteau L'association maladie de Pick et sclérose latérale amyotrophique Encephale 6 1985 259 286
27. B. Brownell, D.R. Oppenheimer, and J.T. Hughes The central nervous system in motor neuron disease J Neurol Neurosurg Psychiatry 33 1970 3388 4357
28. L.I. Bruijn, M.F. Beal, and M.W. Becher Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superoxide dismutase 1 mutant Proc Natl Acad Sci 48 1997 337 339
29. A. Brun Frontal lobe degeneration of non-Alzheimer type Neuropathol Arch Gerontol Geriatr 6 1987 193 208
30. A. Brusa, G.L. Marcandi, and O. Bugiani Progressive supranuclear palsy 1979: an overview Ital J Neurol Sci 4 1980 205 222
31. L. Buée, T. Bussiere, and V. Buee-Scherrer Tau protein isoforms, phosphorylation and role in neurodegenerative disorders Brain Res Rev 33 2000 95 130
32. O. Bugiani, J.R. Murrell, and G. Giaccone Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau J Neuropathol Exp Neurol 58 1999 667 677
33. E. Buratti, T. Dork, E. Zuccatto, F. Pagani, M. Romano, and F.E. Baralle Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping EMBO J 20 2001 1774 1784
34. D.J. Burn, and A.J. Lees Progressive supranuclear palsy: where are we now? Lancet Neurol 1 2002 359
35. J.N. Burrow, and P.C. Blumbergs Substantia nigra degeneration in motor neuron disease: a quantitative study Aust N Z J Med 22 1992 469 472
36. A. Caceres, and K.S. Kosik Inhibition of neurite polarity by tau antisense oligonucleotides in primary cerebellar neurons Nature 343 1990 461 463
37. N.J. Cairns, E.H. Bigio, and I.R.A. Mackensie Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the consortium for frontotemporal lobar degeneration Acta Neuropathol 114 2007 5 22
38. D.B. Calne, A. Eisen, E. McGeer, and P. Spencer Alzheimer's disease. Parkinson's disease and motoneurone disease: abiotropic interaction between ageing and environment? Lancet 2 1986 1067 1070
39. I. Cantuti-Castelvetri, C.E. Keller-McGandy, and D.S. Albers Expression and activity of antioxydants in the brain in porgressive supranuclear palsy Brain Res 930 2002 170 181
40. R.J. Caselli, A.J. Windebank, and R.C. Petersen Rapidly progressive aphasic dementia and motor neuron disease Ann Neurol 33 1993 200 207
41. P. Castaigne, F. Lhermitte, J. Cambier, R. Escourolle, and P. Le Bigot Étude neuropathologique de 61 observations de sclérose latérale amyotrophique. Discussion nosologique Rev Neurol 127 1972 401 414
42. J.L. Chang, C. Lomen-Hoerth, and J. Murphy A Voxel-based morphometry study of patterns of brain atrophy in ALS and ALS/FTLD Neurology 65 2005 75 80
43. Chen KM, Chase TN. Parkinsonims-dementia. In: Vinken PJ, Bruyn GW, Klawans HL (eds.). Handbook of clinical neurology, vol 49. Revised series 5. Amsterdam: Elsevier, 1985, 167-183.
44. Y.Z. Chen, C.L. Bennett, and H.M. Huynh DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4) Am J Hum Genet 74 2004 1128 1135
45. J. Choi, H.D. Rees, S.T. Weintraub, A.I. Levey, L.S. Chin, and L. Li Oxidative modifications and aggregation of Cu, Zn-superoxide dismutase associated with Alzheimer and Parkinson diseases J Biol Chem 280 2005 11648 11655
46. C. Conrad, A. Andreadis, and J.G. Trojanowski Genetic evidence for the involvement of tau in progressive supranuclear palsy Ann Neurol 41 1997 277 281
47. J. Constantinidis Syndrome familial: association de maladie de Pick et sclérose latérale amyotrophique Encephale 13 1987 283 293
48. S.E. Daniel, M.S. deBruin, and A.J. Lees The clinical and pathological spectrum of Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy): a reappraisal Brain 118 1995 759 770
49. C. Davison Pallido-pyramidal disease J Neuropathol Exp Neurol 13 1954 50 59
50. A. Delacourte, A. Defossez, I. Ceballos, A. Nicole, and P.M. Sinet Preferential localization of copper zinc superoxide dismutase in the vulnerable cortical neurons in Alzheimer's disease Neurosci Lett 92 1988 247 253
51. J. Desai, and M. Swash Extrapyramidal involvement in amytrophic lateral sclerosis: backward falls and retropulsion J Neurol Neurosurg Psychiatry 67 1999 214 216
52. Désarnaud S. (2005). Étude scintigraphique de l'atteinte extrapyramidale au cours de la sclérose latérale amyotrophique. Thse de doctorat en médecine. Université René-Descartes- Paris-V.
53. M. Dib, C. Garrel, A. Favier, V. Robin, and C. Desnuelle Can malondialdehyde be used as a biological marker of progression in neurodegenerative disease? J Neurol 249 2002 367 374
54. D.W. Dickson Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration J Neurol 246 Suppl. 2 1999 II6 II15
55. D.W. Dickson, K.A. Josephs, and C. Amador-Ortiz TDP-43 in differential diagnosis of motor neuron disorders Acta Neuropathol 114 2007 171 179
56. D.G. Drubin, and M.W. Kirschner Tau protein function in living cells J Cell Biol 103 1986 2739 2746
57. A. Eisen, and D. Calne Amyotrophic lateral sclerosis, Parkinson's disease and Alzheimer'disease: philogenetic disorders of the human neocortex sharing many characteristics Can J Neurol Sci 19 Suppl. 1 1992 117 123
58. T.S. Elizan, A. Hirano, B.M. Abrams, R.L. Need, C. van Nuis, and L.T. Kurland Amyotrophic lateral sclerosis and parkinsonism-dementia complex of Guam Arch Neurol 14 1966 256 368
59. L.S. Forno, and T.J. O'Flanagan Amyotrophic lateral sclerosis of a Guam type in a US veteran Neurology 23 1973 876 880
60. N.L. Foster, K. Wilhelmsen, and A.A. Sima Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference Ann Neurol 41 1997 706 715
61. I. Fridovich Superoxide radical and superoxide dismutases Annu Rev Biochem 64 1995 97 112
62. T. Furukawa Clinical and epidemiological studies on amyotrophic lateral sclerosis Osaka Daigaku Shigaku Zasshi 11 1959 4087 4099
63. W.R. Galpern, and A.E. Lang Interface between tauopathies and synucleinopathies: a tale of two proteins Ann Neurol 59 2006 449 458
64. R.M. Garruto, C. Gajdusek, and K.M. Chen Amyotrophic lateral sclerosis among Chamorro migrants from Guam Neurology 8 1980 612 619
65. R.M. Garruto, R.T. Yanagihara, and D.C. Gajdusek Disappearance of high-incidence amyotrophic lateral sclerosis and parkinsonism-dementia on Guam Neurology 35 1985 193 198
66. G.G. Gascon, P. Chavis, and A. Yaghmour Familial childhood primary lateral sclerosis with associated gaze paresis Neuropediatrics 26 1995 313 319
67. F. Geser, M.J. Winton, and L.K. Kwong Pathological TDP-43 in parkinson-dementia complex and amyotrophic lateal sclerosis of Guam Acta Neuropathol 115 2008 135 145
68. B. Ghetti, M.L. Hutton, and Z.K. Wszolek Frontotemporal dementia and parkinsonism linked to chromosome 17 associated with tau gene mutations (FTDP-17T) D.W. Dickson Neurodegeneration: the molecular pathology of dementia and movement disorders 2003 ISN Neuropath Press Basel 86 102
69. Gitcho MA, Baloh RH, Chakraverty S, et al. TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol, in press (epub 20 Feb 2008).
70. M. Goedert, and R. Jakes Mutations causing neurodegenerative tauopathies Biochim Biophys Acta 1739 2005 240 250
71. M. Goedert Tau gene mutations and their effects Mov Disord 20 Suppl. 12 2005 S45 S52
72. L.I. Golbe, and P.H. Davis Progressive supranuclear palsy: recent advances J. Jankovic E. Tolosa Parkinson's disease and movement disorders 1988 Urban and Schwarzenberg Baltimore 121 130
73. L.I. Golbe, and D.W. Dickson Familial autopsy-proven progressive supranuclear palsy Neurology 45 Suppl. 4 1995 A255
74. J.S. Goldman, J.M. Farmer, and E.M. Wood Comparison of family histories in FTLD subtypes and related tauopathies Neurology 65 2005 1817 1819
75. F. Gray, C. De Baecque, M. Serdaru, and R. Escourolle Pallido-luyso-nigral atrophy and amyotrophic lateral sclerosis Acta Neuropathol Suppl 7 1981 348 351
76. F. Gray, J.F. Eizenbaum, R. Gherardi, J.D. Degos, and J. Poirier Luyso-pallido-nigral atrophy and amyotrophic lateral sclerosis Acta Neuropathol (Berl) 66 1985 78 82
77. G. Guillain, and T. Alajouanine Sclérose latérale amyotrophique avec contracture intense du type extrapyramidale (hypertonie plastique et exagération des réflexes de posture). Discussion de son étiologie encéphalitique Rev Neurol 45 1926 337 342
78. S. Hadano, C.K. Hand, and H. Osuga A gene encoding a putative GTPase regulator is mutated in familial amyotrophic laterals sclerosis 2 Nat Genet 29 2001 166 173
79. J.A. Hainfellner, P. Pilz, H. Lassmann, G. Ladurner, and H. Budka Diffuse Lewy body disease as substrate of primary lateral sclerosis J Neurol 242 1995 59 63
80. C.K. Hand, J. Khoris, and F. Salachas A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q Am J Hum Genet 70 2002 251 256
81. C. Hand, and G.A. Rouleau Familial amyotrophic lateral sclerosis Muscle Nerve 25 2002 139 152
82. D.G. Harvey, R.M. Torack, and H.E. Rosenbaum Amyotrophic lateral sclerosis with ophtalmoplegia. A clinicopathologic study Arch Neurol 36 1979 615 617
83. K. Hasegawa, H. Kowa, and S. Yagishita Extrapyramidal system involvement in motor neuron disease J Neurol Sci 108 1992 137 148
84. J.J. Hauw, S.E. Daniel, and D. Dickson Preliminary NINDS neuropathologic criteria for the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy) Neurology 44 1994 2015 2019
85. J.J. Hauw, and Y. Agid Progressive supranuclear palsy (PSP) or Steele-Richardson-Olszewski D.W. Dickson Neurodegeneration: the molecular pathology of dementia and movement disorders 2003 ISN Neuropath Press Basel 103 114
86. A. Hentati, K. Ouahchi, and M.A. Pericak-Vance Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers Neurogenetics 2 1998 55 60
87. P. Heutink, M. Stevens, and P. Rizzu Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: a genetic and clinicopathological study of three Dutch families Ann Neurol 41 1997 150 159
88. T. Hideyama, T. Momose, J. Shimizu, S. Tsuji, and S. Kwak A positron emission tomography study on the role of nigral lesions in parkinsonism in patients with amyotrophic lateral sclerosis Arch Neurol 63 2006 1719 1722
89. A. Hirano, L.T. Kurland, and R.S. Krooth Parkinsonism-dementia complex, an endemic disease on the island of Guam. I. Clinical features Brain 84 1961 642 661
90. A. Hirano, N. Malamud, and L.T. Kurland Parkinsonism-dementia complex, an endemic disease of the island of Guam. II. Pathological features Brain 84 1961 662 679
91. A. Hirano, L.T. Kurland, and G.P. Sayre Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells Arch Neurol 16 1967 232 243
92. J.R. Hodges, P. Davis, and J. Xuereb Clinicopathological correlates in frontotemporal dementia Ann Neurol 56 2004 399 406
93. D.S. Horoupian, L. Thal, and R. Katzman Dementia and motor neuron disease: morphometric, biochemical and Golgi studies Ann Neurol 16 1984 305 313
94. B.A. Hosler, T. Siddique, and P.C. Sapp Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 JAMA 284 2000 1664 1669
95. H. Houlden, M. Baker, and J. Adamson Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia Ann Neurol 46 1999 243 248
96. A.J. Hudson Amyotrophic lateral sclerosis and its association with dementia, parkinsonism and other neurological disorders Brain 104 1981 217 247
97. A.J. Hughes, S.E. Daniel, L. Kilford, and A.J. Lees Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases J Neurol Neurosurg Psychiatry 55 1992 181 184
98. A.J. Hughes, Y. Ben-Schlomo, S.E. Daniel, and A.J. Lees What features improve the accuracy of clinical diagnosis in idiopathic Parkinson's disease: a clinico-pathological study Neurology 42 1992 1142 1146
99. R. Hunt Progressive atrophy of the globus pallidum (primary atrophy of the pallidal system). A system disease of the paralysis agitans type, characterized by atrophy of the motor cells of the corpus striatum. A contribution to the functions of the corpus striatum Brain 40 1917 58 148
100. M. Hutton, C.L. Lendon, and P. Rizzu Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 Nature 393 1998 702 705
101. M. Inoue, Y. Kojima, H. Satoi, F. Makino, M. Kanda, and H. Shibasaki Case presenting both clinical features of progressive supranuclear palsy and amyotrophic lateral sclerosis Rinsho Shinkeigaku 46 2006 390 394
102. E. Iseki, T. Matsumura, and W. Marui Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells Acta Neuropathol 102 2001 202 285
103. M. Jackson, G. Lennox, and J. Lowe Motor neuron disease inclusion dementia Neurodegeneration 5 1996 339 350
104. H.F. Jafari-Schluep, J. Khoris, and V. Mayeux-Portas Les anomalies du gne superoxyde dismutase 1 dans le sclérose latérale amytotrophique familiale corrélations phénotype/génotype et implications pratiques. L'expérience franaise et revue de la littérature Rev Neurol 160 2004 44 50
105. K. Jellinger Pallidal, pallidonigral and pallido luysio nigral degenerations including association with thalamic and dentate degenerations P.J. Vinken G.W. Bruyn H.L. Klawans Handbook of clinical neurology 5 1986 Elsevier Amsterdam 445 463
106. G.V. Johnson, and W.H. Stoothoff Tau phosphorylation in neuronal cell function and dysfunction J Cell Sci 117 2004 5721 5729
107. K.A. Josephs, R.C. Petersen, and D.S. Knopmpan Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP Neurology 66 2006 41 48
108. K.A. Josephs, O. Katsuse, and D.A. Beccano-Kelly Atypical progressive supranuclear palsy with corticobasal tract degeneration J Neuropathol Exp Neurol 65 2006 396 405
109. H. Katsuki, M. Tomita, and C. Takenaka Superoxide dismutase activity in organotypic midbrain-striatum co-cultures is associated with resistance of dopaminergic neurons to excitotoxicity J Neurochem 76 2001 1136 1145
110. S. Kato, M. Oda, and H. Tanabe Diminution of dopaminergic neurons in the substantia nigra of sporadic lateral sclerosis Neuropathol Appl Neurobiol 19 1993 300 304
111. S. Kato, M. Oda, M. Murahashi, and N. Suda Motor neuron disease with involvement of the pallido-luysio-nigral system and mesencephalic tegmentum Clin Neuropathol 14 1995 241 244
112. A. Kertesz, P. McMonagle, M. Blair, W. Davidson, and D.G. Munoz The evolution and pathology of frontotemporal dementia Brain 128 2005 1996 2005
113. A. Kertesz Progress in clinical neurosciences: frontotemporal dementia-Pick's disease Can J Neurol Sci 33 2006 141 148
114. M. Kobayashi, K. Ikeda, M. Kinoshita, and Y. Iwasaki Amyotrophic lateral sclerosis with supranuclear ophtalmoplegia and rigidity Neurol Res 21 1999 661 664
115. Y. Kokubo, and S. Kuzuhara Neurofibrillary tangles in ALS and parkinsonism-dementia complex focus in Kii, Japan Neurology 63 2004 2399 2401
116. T. Komori, N. Arai, and M. Oda Astrocytic plaques and tufts of abnormal fibers do not coexist in corticobasal degeneration and progressive supranuclear palsy Acta Neuropathol 96 1998 401 408
117. V. Kostic, M.E. Gurney, H.X. Deng, T. Siddique, C.J. Epstein, and S. Przedborski Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosis Ann Neurol 41 1997 497 504 (Pubitemid 27169189)
118. S. Kumar-Singh, and C. van Broeckhoven Frontotemporal Lobar degeneration: current concepts in the light of recent advances Brain Pathol 17 2007 104 114
119. C.B. Kunst Complex genetics of amyotrophic lateral sclerosis Am J Hum Genet 75 2004 933 947
120. L.T. Kurland, and D.W. Mulder Epidemiologic investigation of amyotrophic lateral sclerosis. Preliminary report on geographic distribution, with special reference to the Mariana islands, including clinical and pathological observations Neurology 4 1954 355 378
121. L.T. Kurland Amyotrophic lateral sclerosis and Parkinson's disease complex on Guam linked to an environmental neurotoxin TINS 11 1988 51 54
122. S. Kuroda, M. Chuda, H. Ikeda, S. Otsuki, and J. Tateishi Olivo-ponto-cerebellar atrophy with notable changes of the striato-nigral and pyramidal system Rinsho Shinkeigaku 17 1977 336 343
123. S. Kuzuhara, Y. Kokubo, and R. Sasaki Familial amyotrophic lateral sclerosis and Parkinsonism-dementia complex of the Kii Peninsula of Japan: clinical and neuropathological study and tau analysis Ann Neurol 49 2001 501 511
124. L.K. Kwong, M. Neumann, D.M. Sampathu, V.M.Y. Lee, and J.Q. Trojanowski TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease Acta Neuropathol 114 2007 63 70
125. L. Lanotte, G. Barroche, L. Taillandier, and J.C. Lacour Familial progressive supranuclear palsy Mov Disord 11 1996 126
126. T. Lawyer Jr., and M.G. Netsky Amyotrophic lateral sclerosis: a clinicoanatomic study of 53 cases Arch Neurol Psychiatr 69 1953 171 192
127. T. Lebouvier, P. Damier, and P. Derkinderen Les tauopathies. Lett Neurol 10 2006 14 18
128. A.J. Lees The Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy) C.D. Marsden S. Fahn Movements disorders 2 1987 Butterworths London 272 287
129. N. Le Forestier, T. Maisonobe, and A. Piquard Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature Brain 124 2001 1989 1999
130. K.L. Leenders, S.J. Frackowiak, and A.J. Lees Steele-Richardson-Olszewski syndrome. Brain energy metabolism, blood flow and fluorodopa uptake measured by positron emission tomography Brain 111 1988 615 630
131. R. Legrand, M. Linquette, F. Delahousse, and A. Gérard propos d'un nouveau cas d'association d'une maladie de Parkinson et d'une sclérose latérale amyotrophique Soc Fr 1959 191 193
132. Litvan I Agid Y, Calne D et al. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology 1996a;47: 1-9.
133. I. Litvan, J.J. Hauw, and J.J. Bartko Validity and reliability of the prelimary NINDS neuropathologic criteria for progressive supranuclear palsy and related disorders J Neuropathol Exp Neurol 55 1996 97 105
134. I. Litvan, C.G. Goetz, and F. Jankovic What is the accurancy of the clinical diagnosis of multiple system atrophy? A clinicopathologic study Arch Neurol 54 1997 937 944 (Pubitemid 27330401)
135. I. Litvan, G. Campbell, and C.A. Mangone Which clinical features differenciate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? Brain 120 1997 65 74
136. C. Lomen-Hoerth, T. Anderson, and B. Miller The overlap of amyotrophic lateral sclerosis and frontoremporal dementia Neurology 59 2002 1007 1009
137. C. Lomen-Hoerth, J. Murphy, S. Langmore, J.H. Kramer, R.K. Olney, and B. Miller Are amyotrophic lateral sclerosis patients cognitively normal? Neurology 60 2003 1094 1097
138. P. Lo Presti Functionnal implications for the microtubule-associated protein tau: localization in oligodendrocytes Proc Natl Acad Sci USA 92 1995 10369 10373
139. S. Lovestone, and D.M. McLoughlin Protein aggregates and dementia: is there a common toxicity? J Neurol Neurosurg Psychiatry 72 2002 152 161
140. J. Lowe New pathological findings in amyotrophic lateral sclerosis J Neurol Sci 124 1994 38 51
141. J. Lowe, G. Lennox, and P.N. Leigh Disorders of movement and system degenerations D.I. Graham P.L. Lantos Greenfield's neuropathology 6th ed. 1997 Arnold London 280 366
142. M.A. Lovell, W.D. Ehmann, S.M. Butler, and W.R. Markesbery Elevated thiobarbituric acid-reactive substances and antioxidant enzyme activity in the brain in Alzheimer' disease Neurology 45 1995 1594 1601
143. M.A. Lovell, W.D. Ehmann, S.M. Butler, and W.R. Markesbery Elevated thiobarbituric acid-reactive substances and antioxidant enzyme activity in the brain in Alzheimer's disease Neurology 45 1997 1594 1601
144. T. Lynch, M. Sano, and K.S. Marder Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex Neurology 44 1994 1878 1884
145. N. Mabuchi, H. Watanabe, and N. Atsuta Primary lateral sclerosis presenting parkinsonian symptoms without nigrostriatal involvement J Neurol Neurosurg Psychiatry 75 2004 1768 1771
146. G.M. McKhann, M.S. Albert, M. Grossman, B. Miller, D. Dickson, and J.Q. Trojanowski Clinical and pathological diagnosis of frontotemporal dementia: report of the group on frontotemporal dementia disease Arch Neurol 58 2001 1803 1809
147. E.R. Maher, and A.J. Lees The clinical features and natural history of the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy) Neurology 36 1986 1005 1008
148. D. Majoor-Krakauer, P. Mulder, L.P. Rowland, and R. Ottman A link between ALS and short residence on Guam Neurology 64 2005 1819 1820
149. L.J. Martin Mitochondriopathy in Parkinson disease and amyotrophic lateral sclerosis J Neuropathol Exp Neurol 65 2006 1103 1110
150. O. Martinaud, A. Laquerrire, and L. Guyant-Maréchal Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family Acta Neuropathol 110 2005 84 92
151. T. Masini, N. Canal, and G.C. Guazzi Poliomyélite chronique et dégénérescence nigrique se présentant cliniquement comme une amyotrophie progressive spinale Psychiatry Neurol 150 1965 21 41
152. P.J. Massman, J. Sims, N. Cooke, L.J. Haverkamp, V. Appel, and S.H. Appel Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis J Neurol Neurosurg Psychiatry 61 1996 450 455
153. S. Matsumoto, A.N. Hirano, and S. Gooto Spinal cord neurofibrillary tangles of Guamanian amyotrophic lateral sclerosis and parkinsonism-dementia- complex: an immunohistochemical study Neurology 40 1990 975 979
154. Y. Mitsuyama, and S. Takamiya Presenile dementia with motor neuron disease in Japan Arch Neurol 36 1979 592 593
155. Y. Mitsuyama Presenile dementia with motor neuron disease in Japan: clinico-pathological review of 26 cases J Neurol Neurosurg Psychiatry 47 1984 953 959
156. Y. Mitsuyama, H. Kogoh, and K. Ata Progressive dementia with motor neuron disease. An additional case report and neuropathological review of 20 cases in Japan Eur Arch Psychiatry Neurol Sci 235 1985 1 8
157. H. Mori Pathologic changes of progressive supranuclear palsy, corticobasal dgeneration, and multiple system atrophy J Neurol 253 Suppl. 3 2006 41 46
158. K. Morita, H. Kaiya, T. Ikeda, and M. Namba Presenile dementia combined with amyotrophy: a review of 34 Japanese cases Arch Gerontol Geriatr 6 1987 263 277
159. K. Morita, A. Al-Chalabi, and P.M. Andersen A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia Neurology 66 2006 839 844
160. H.R. Morris, S. Al-Sarraj, and C. Schwab A clinical and pathological study of motor neurone disease on Guam Brain 124 2001 2215 2222
161. M.J. Mossakowski, and K. Rentawek Amyotrophic lateral sclerosis with generalized neuroaxonal degeneration and selective involvement of the nigropallidal system Neuropatol Pol 25 1987 539 553
162. G. Moya, G. Miranda-Nieves, and M. Perez Sotelo Un cas familial d'amyotrophie spinale progressive montrant une atteinte histologique, cliniquement muette, du pallidum, du locus niger, du noyau de Luys et du faisceau de Goll Acta Neurol Belg 69 1969 1002 1012
163. G. Munch, M. Gerlach, J. Sian, A. Wong, and P. Riederer Advanced glycation end products in neurodegeneration: more than early markers of oxidative stress? Ann Neurol 44 1998 S85 S88
164. C. Münch, R. Sedlmeler, and T. Meyer Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS Neurology 63 2004 724 726
165. C. Münch, A. Rosenbohm, and A.D. Sperfeld Heterezygous R110K mutation of the DCTN1 gene in a family with ALS and FTD Ann Neurol 58 2005 770 780
166. D. Munoz-Garcia, and S.K. Ludwin Classic and generalized variants of Pick's disease: clinicopathological, ultrastructural, and immunocytochemical comparative study Ann Neurol 16 1984 467 480
167. D.G. Munoz, D.W. Dickson, C. Bergeron, I.R.A. Mackenzie, A. Delacourte, and V. Zhukareva The neuropathy and biochemistry of frontotemporal dementia Ann Neurol 54 Suppl. 5 2003 S24 S28
168. J. Murphy, R. Henry, and S. Langmore Continuum of frontal lobe impairment in amyotrophic lateral sclerosis Arch Neurol 64 2007 530 534
169. Y. Nagano, T. Tsubaki, and K.M. Chen Amyotrophic lateral sclerosis on Guam. Part 2 Clin Neurol 17 1977 582 588
170. D. Neary, J.S. Snowden, D.M. Mann, B. Northen, P.J. Goulding, and N. Macdermott Frontal lobe dementia and motor neuron disease J Neurol Neurosurg Psychiatry 53 1990 23 32
171. D. Neary, J.S. Snowden, and D. Dickson Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria Neurology 51 1998 1546 1554
172. M. Neumann, D.M. Sampathu, and L.K. Kwong Ubiquitinated TDP-43 in frontotemporal degeneration and amyotrophic lateral sclerosis Science 314 2006 130 133
173. K. Noda, S. Katayama, C. Watanabe, Y. Yamamura, and S. Nakamura Gallyas and tau-positive glial structures in motor neuron disease with dementia Clin Neuropathol 18 1999 218 225
174. H. Oba, A. Yagishita, and Terada New and reliable MRI diagnosis for progressive supranuclear palsy Neurology 64 2005 2050 2055
175. P. Odetti, S. Garibaldi, and R. Norese Lipoperoxidation is selectively involved in progressive supranuclear palsy J Neuropathol Exp Neurol 59 2000 393 397
176. K. Okamoto, S. Hirai, M. Shoji, Y. Senoh, and T. Yamazaki Axonal swelling of the corticospinal tracts in amyotrophic lateral sclerosis Acta Neuropathol 80 1991 222 226
177. B. Okuda, T. Yamamoto, M. Yamasaki, K. Maya, and T. Imai Motor neuron disease with slow eye movements and vertical gaze palsy Acta Neurol Scand 85 1992 71 76
178. H. Okumura, K.M. Chen, and L.T. Kurland Recent epidemiologic study of amyotrophic lateral sclerosis (ALS) and parkinsonism-dementia complex (PDC) in Guam island Jpn J Clin Ecol 4 1995 355 378
179. K. Oyanagi The nature of the parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam and magnesium deficiency Parkinsonism Relat Disord 11 2005 S17 S23
180. K. Oyanagi, E. Kawakami, and K. Kikuchi-Horie Magnesium deficiency over generations in rats with special references to the pathogenesis of the parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam Neuropathology 26 2006 115 128
181. S. Papapetropoulos, T. Scaravilli, and H. Morris Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology Neurology 64 2005 731 733
182. J. Patrikios Sclérose latérale amyotrophique avec mouvements involontaires des doigts et du poignet gauche de caractre extrapyramidal Rev Neurol 85 1951 60 62
183. G.M. Peavy, A.G. Herzog, N.P. Rubin, and M.M. Mesulam Neuropsychological aspects of dementia of motor neuron disease: a report of two cases Neurology 42 1992 1004 1008
184. Y.S. Piao, C.F. Tan, and K. Iwagana Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease Acta Neuropathol 110 2005 600 609
185. C.C. Plato, R.M. Garruto, and D. Galasko Amyotrophic lateral sclerosis ad parkinsonism-dementia complex of Guam: changing incidence rates during the past 60 years Am J Epidemiol 157 2003 149 157
186. P. Poorkaj, T.D. Bird, and E. Wijsman Tau is a candidate gene for chromosome 17 frontotemporal dementia Ann Neurol 43 1998 815 825
187. P. Poorkaj, D. Tsuang, and E. Wijsman Tau as a susceptibility gene for amyotrophic lateral sclerosis-parkinsonism dementia complex of Guam Arch Neurol 58 2001 1871 1878
188. P.F. Pradat, C. Dupel-Pottier, and L. Lacomblez Case report of pallido-pyramidal disease with supplementary motor area involvement Mov Disord 16 2001 762 764
189. I. Puls, C. Jonnakuty, and B.H. LaMonte Mutant dynactin in motor neuron disease Nat Genet 33 2003 455 456
190. A.I. Qureshi, G. Wilmot, B. Dihenia, J.A. Schneider, and D.A. Krendel Motor neuron disease with parkinsonism Arch Neurol 53 1996 987 991
191. L. Rampello, V. Butta, and R. Raffaele Progressive supranuclear palsy: a systematic review Neurobiol Dis 20 2005 179 186
192. S. Riku, and Y. Hashizume A clinico-pathological study of multiple system atrophy, with special reference to its striato-nigral lesions and motor neuron involvements Rinsho Shinkeigaku 24 1984 552 561
193. G.M. Ringholz, and S.R. Greene The relationship between amyotrophic lateral sclerosis and frontotemporal dementia Curr Neurol Neurosci Rep 6 2006 387 392
194. J. Robertson, T. Sanelli, and S. Xiao Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS Neurosci Lett 420 2007 128 132
195. G. Rosati, L. Pinna, and E. Granieri Studies of epidemiological, clinical, etiological aspects of ALS disease in Sardinia, Southern Italy Acta Neurol Scand 55 1977 231 244
196. D.R. Rosen, T. Siddique, and D. Patterson Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis Nature 362 1993 59 62
197. S.M. Rosso, and J.C. van Swieten New developments in frontotemporal dementia and parkinsonism linked to chromosome 17 Curr Opin Neurol 15 2002 423 428
198. M. Ruberg, F. Javoid-Agid, and E. Hirsch Dopaminergic and cholinergic lesions in progressive supranuclear palsy Ann Neurol 18 1985 523 529
199. D.M. Ruddy, M.J. Parton, and A. Al-Chalabi Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q Am J Hum Genet 73 2003 390 396
200. G. Rütenik Familiäre amyotrophische lateralsklerose Arch Psychiatr Nervenkr 107 1938 248 264
201. M. Sakai, Y. Hashizume, T. Muroga, N. Murakami, and H. Yamamoto Neuropathological studies of familial amyotrophic lateral sclerosis with special reference to systemic degeneration of dentato-rubral system and neuronal loss of Onulf's nuclei Clin Neurol (Tokyo) 28 1988 1107 1205
202. T. Sanelli, S. Xiao, P. Horne, J. Bilbao, L. Zinman, and J. Robertson Evidence that TDP-47 is not the major ubiquitinated target within the pathological inclusions of amyotrophic lateral sclerosis J Neuropathol Exp Neurol 66 12 2007 1147 1153
203. P.C. Sapp, B.A. Hosler, and D. McKenna-Yasek Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis Am J Hum Genet 73 2003 397 403
204. T. Scaravilli, E. Tolosa, and I. Ferrer Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting Mov Disord 20 2005 S21 S28
205. H.P. Schmitt, W. Emser, and C. Heimes Familial occurence of amyotrophic lateral sclerosis, parkinsonism, and dementia Ann Neurol 16 1984 642 648
206. A. Schrag, C.D. Good, and K. Miszkiel Differenciation of atypical parkinsonian syndromes with routine MRI Neurology 54 2000 697 702
207. J.B. Schulz, M. Skalej, and D. Wedekind Magnetic resonance imaging-based volumetry differenciates idiopathic Parkinson's syndrome from multiple system atrophy and progressive supranuclear palsy Ann Neurol 45 1999 65 74
208. N. Sergeant, A. Wattez, and A. Delacourte Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively "exon 10" isoforms J Neurochem 72 1999 1243 1249 (Pubitemid 29085040)
209. G.T. Serratrice, M. Toga, and J.F. Pellissier Chronic spinal muscular atrophy and pallidonigral degeneration. Report of a case Neurology 33 1983 306 310
210. S. Sha, C. Hou, I.V. Viskontas, and B.L. Miller Are frontotemporal lobar degeneration, progressive supranuclear palsy and corticobasal degeneration distinct diseases? Nat Clin Pract Neurol 2 2006 658 665
211. Shiraki H, Yase Y. (1975). Amyotrophic lateral sclerosis in Japan. In: Vinken PJ, Bruyn GW, Klawans HL. (eds.). Handbook of clinical neurology, p. 353-419.
212. M.C. Smith Nerve fiber degeneration in the brain in amyotrophic lateral sclerosis J Neurol Neurosurg Psychiatry 23 1960 269 282
213. R.G. Smith, Y.K. Henry, M.P. Mattson, and S.H. Appel Presence of 4-hydroxynonemal in cerebrospinal fluid of patients with sporadic amyotrophic lateral sclerosis Ann Neurol 249 1998 367 374
214. J.S. Snowden, D. Neary, and D.M. Mann Frontotemporal dementia Br J Psychiatry 180 2002 140 143
215. P.S. Spencer, P.B. Nunn, and J. Hugon Guam amyotrophic lateral sclerosis-parkinsonism-dementia linked to a plant excitant neurotoxin Science 237 1987 517 522
216. M.G. Spillantini, T.D. Bird, and B. Ghett Frontotemporal dementia and parkinsonism linked to chromosome 17: a new group of tauopathies Brain Pathol 8 1998 387 402
217. M.G. Spillantini, and M. Goedert Tau mutations in familial frontotemporal dementia Brain 123 2000 857 859
218. S. Spina, J.R. Murrell, and E.D. Huey Clinicopathologic features of fronto temporal dementia with progranulin sequence variation Neurology 13 2007 820 827
219. P.M. Stanford, G.M. Halliday, and W.S. Brooks Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene-Expansion of the disease phenotype caused by tau gene mutations Brain 123 2000 880 893
220. P.M. Stanford, W.S. Brooks, and E.T. Teber Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies J Neurol 251 2004 1098 1104
221. J.C. Steele, J.C. Richardson, and J. Olszewski Progressive supranuclear palsy: a heterogenous degeneration involving the brain stem, basal ganglia, and cerebellum with vertical gaze and supraunuclear palsy, nuchal dystonia and dementia Arch Neurol 10 1964 333 359
222. J.C. Steele, D. Caparros-Lefebvre, A.J. Lees, and O.W. Sacks Progressive supranuclear palsy and its relation in pacific foci of the parkinsonism-dementia complex and Guadeloupean parkinsonism Parkinsonism Relat Disord 9 2002 39 54
223. M.J. Strong, G.M. Grace, and J.B. Orange A prospective study of cognitive impairment in ALS Neurology 53 1999 1665 1670
224. M.J. Strong, C. Lomen-Hoerth, R.J. Caselli, E.H. Bigio, and W. Yang Cognitive impairment. FTD and motor neuron disease Ann Neurol 54 2003 S20 S23
225. M.J. Strong, W. Yang, W.L. Strong, C. Leystra-Lantz, H. Jaffe, and H.C. Pant Tau protein hyperphosphorylation in sporadic ALS with cognitive impairment Neurology 66 2006 1770 1771
226. N. Sunohara, M. Mukoyama, H. Funamoto, N. Kamei, H. Tomi, and E. Satoyoshi Supranuclear paralysis preventing lid closure in amyotrophic lateral sclerosis Jpn J Med 28 1989 515 519
227. H. Takahashi, B.J. Snow, M.H. Bhatt, R. Peppard, A. Eisen, and D.B. Calne Evidence for a dopaminergic deficit in sporadic amyotrophic lateral sclerosis on positron emission scanning Lancet 342 1993 1016 1018
228. K. Talbot, and O. Ansorge Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease Hum Mol Genet 15 2006 R182 R187
229. C.F. Tan, H. Eguchi, and A. Tagawa TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation Acta Neuropathol (Berl) 113 2007 535 542
230. J. Tanaka, H. Nakamara, Y. Tabuchi, and K. Takahashi Familial amyotrophic lateral sclerosis: features of multisystem degeneration Acta Neuropathol 64 1984 22 29
231. J.W. Tetrud, L.I. Golbe, L.S. Forno, and P.M. Farmer Autopsy-proven progressive supranuclear palsy in two siblings Neurology 46 1996 931 934
232. E. Tolosa, F. Valldeoriola, and P. Pastor Progressive supranuclear palsy J. Jankovic E. Tolosa Parkinson disease and movement disorders 4th ed. 2002 Lippincott Williams &Wilkins Philadelphia 152 169
233. C. Tranchant, M.H. Dugay, M. Mohr, P. Wasser, and J.M. Warter Familial motor neuron disease with Lewy body-like inclusions in the substantia nigra, the subthalamic nucleus, and the globus pallidus J Neurol Sci 108 1992 18 23
234. S. Uematsu Amyotrophic lateral sclerosis and its mental symptoms Shindan Chiryo 22 1935 838 844
235. P.N. Valdmanis, N. Dupre, and J.P. Bouchard Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p Arch Neurol 64 2007 240 245
236. L. van Bogaert Aspects cliniques et pathologiques des atrophies pallidales et pallido-luysiennes progressives J Neurol Neurosurg Psychiatry 9 1946 125 157
237. L. van Bogaert, and M.A. Radermecker Scléroses latérales amyotrophiques typiques et paralysies agitantes héréditaires, dans une même famille, avec une forme de passage possible pour les deux affections Mschr Psychiatr Neurol 127 1954 185 203
238. Bonduelle M. Amyotrophic lateral sclerosis. In: handbook of clinical neurology. Vinker and Bruyn, Ed. Amsterdam. 1975;22(13):281-338.
239. Bonduelle MM, Bouygues P, Delahousse J, Faveret C. Évolution simultanée chez un même malade d'une maladie de Parkinson et d'une sclérose latérale amyotrophique. Discussion. Soc Fr Neurol, séance du 4 Juin, 1959, 63-66.
240. R. Vitaliani, T. Scaravilli, and E. Egarter-Vigl The pathology of the spinal cord in progressive supranuclear palsy J Neuropathol Exp Neurol 61 2002 268 274
241. O.J.M. Vogels, W.J.G. Oyen, and B.G.M. van Engelen Decreased striatal dopamine-receptor binding in sporadic ALS: glutamate hyperactivity? Neurology 12 1999 1275 1277
242. N. Wakamatsu, T. Yuasa, Y. Souma, T. Watanabe, and T. Miyatake A case of amyotrophic lateral sclerosis associated with clinical features of progressive supranuclear palsy Rinsho Shinkeigaku 29 1989 1173 1175
243. I.S. Wechsler, and C. Davison Amyotrophic lateral sclerosis with mental symptoms Arch Neurol Psychiatr 27 1932 857 880
244. K.C. Wilhelmsen, T. Lynch, E. Pavlou, M. Higgins, and T.G. Nygaard Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22 Am J Hum Genet 55 1994 1159 1165
245. K.C. Wilhelsem, M.S. Forman, and H.J. Rosen 17-q linked frontotemporal dementia-amyotrophic lateral sclerosis without tau mutations with tau and alpha-synuclein inclusions Arch Neurol 61 2004 398 406
246. T.L. Williams, P.J. Shaw, J. Lowe, D. Bates, and P.G. Ince Parkinsonism in motor neuron disease: case report and literature review Acta Neuropathol (Berl) 89 1995 275 283
247. N.W. Winkelman, and M.H. Book Asymptomatic extrapyramidal involvement in Pick's disease Arch Neurol Psychiatr 8 1944 30 42
248. H.K. Wolf, B.J. Crain, and T. Siddique Degeneration of the substantia nigra in familial amyotrophic lateral sclerosis Clin Neuropathol 10 1991 292 296
249. S. Xiao, C. Sato, and T. Kawarai Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis Neurobiol Aging 22 2007 [Epub ahead of print]
250. M. Yamazaki, Y. Arai, and M. Baba Alpha-synuclein inclusions in amygdala in the brains of patients with the parkinsonism-dementia complex of Guam J Neuropathol Exp Neurol 59 2000 585 591
251. Y. Yang, A. Hentati, and H.X. Deng The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis Nat Genet 29 2001 160 165
252. W. Yang, M.M. Sopper, G. Leystra-Lantz, and M.J. Strong Microtubule-associated tau protein positive neuronal and glial inclusions in amyotrophic lateral sclerosis Neurology 61 2003 1766 1773
253. W. Yang, L.C. Ang, and M.J. Strong Tau protein aggregation in the frontal and entorhinal cortices as a function of aging Dev Brain Res 156 2005 127 138
254. M. Yoshida Amyotrophic lateral sclerosis with dementia: the clinicopathological spectrum Neuropathology 24 2004 87 102 (Pubitemid 38391500)
255. J.J. Zarranz, I. Ferrer, and E. Lezcano A novel mutation (K317) in the MAPT gene causes FTDP and motor neuron disease Neurology 64 2005 1587 1595
256. Z.X. Zhang, D.W. Anderson, and N. Mantel Geographic patterns of parkinsonism-dementia complex on Guam. 1956 through 1985 Arch Neurol 47 1990 1069 1074 (Pubitemid 20326662)
257. L.H. Ziegler Psychotic and emotional phenomena associated with amyotrophic lateral sclerosis Arch Neurol Psychiatr 24 1930 930 936
258. M. Zuber, and A. Alpérovitch Maladie de Parkinson et facteurs environnementaux Rev Epidemiol Sante Publique 39 1991 373 387