-
1
-
-
0014400378
-
A light and electron microscopy study of an unusual widespread nuclear inclusion body disease. A possible residuum of an old herpesvirus infection
-
Lindenberg R, Rubinstein LJ, Herman MM, Haydon GB. A light and electron microscopy study of an unusual widespread nuclear inclusion body disease. A possible residuum of an old herpesvirus infection. Acta Neuropathol (Berl) 1968;10:54-73.
-
(1968)
Acta Neuropathol. (Berl.)
, vol.10
, pp. 54-73
-
-
Lindenberg, R.1
Rubinstein, L.J.2
Herman, M.M.3
Haydon, G.B.4
-
2
-
-
0025391287
-
Neuronal intranuclear hyaline inclusion disease: Report of a case and review of the literature
-
Funata N, Maeda Y, Koike M, et al. Neuronal intranuclear hyaline inclusion disease: report of a case and review of the literature. Clin Neuropathol 1990;9:89-96.
-
(1990)
Clin. Neuropathol.
, vol.9
, pp. 89-96
-
-
Funata, N.1
Maeda, Y.2
Koike, M.3
-
4
-
-
0025141647
-
Neuronal intranuclear inclusion disease in a child: Diagnosis by rectal biopsy
-
Goutieres F, Mikol J, Aicardi J. Neuronal intranuclear inclusion disease in a child: diagnosis by rectal biopsy. Ann Neurol 1990; 27:103-106.
-
(1990)
Ann. Neurol.
, vol.27
, pp. 103-106
-
-
Goutieres, F.1
Mikol, J.2
Aicardi, J.3
-
5
-
-
0022872440
-
Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology
-
Haltia M, Tarkkanen A, Somer H, Palo J, Karli H. Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology. Acta Ophthalmol (Copenh) 1986;64: 637-643.
-
(1986)
Acta Ophthalmol. (Copenh.)
, vol.64
, pp. 637-643
-
-
Haltia, M.1
Tarkkanen, A.2
Somer, H.3
Palo, J.4
Karli, H.5
-
6
-
-
0032544414
-
Familial neuronal intranuclear inclusion disease with ubiquitin positive inclusions
-
Kimber TE, Blumbergs PC, Rice JP, et al. Familial neuronal intranuclear inclusion disease with ubiquitin positive inclusions. J Neurol Sci 1998;160:33-40.
-
(1998)
J. Neurol. Sci.
, vol.160
, pp. 33-40
-
-
Kimber, T.E.1
Blumbergs, P.C.2
Rice, J.P.3
-
7
-
-
0021809025
-
Brain neurotransmitter abnormalities in neuronal intranuclear inclusion body disorder
-
Kish SJ, Gilbert JJ, Chang LJ, Mirchandani L, Shannak K, Hornykiewicz O. Brain neurotransmitter abnormalities in neuronal intranuclear inclusion body disorder. Ann Neurol 1985;17:405-407.
-
(1985)
Ann. Neurol.
, vol.17
, pp. 405-407
-
-
Kish, S.J.1
Gilbert, J.J.2
Chang, L.J.3
Mirchandani, L.4
Shannak, K.5
Hornykiewicz, O.6
-
8
-
-
0022454794
-
Adult-onset neuronal intranuclear hyaline inclusion disease
-
Munoz-Garcia D, Ludwin SK. Adult-onset neuronal intranuclear hyaline inclusion disease. Neurology 1986;36:785-790.
-
(1986)
Neurology
, vol.36
, pp. 785-790
-
-
Munoz-Garcia, D.1
Ludwin, S.K.2
-
9
-
-
0034088724
-
Neuronal intranuclear hyaline inclusion disease with polyglutamine-immunoreactive inclusions
-
Takahashi J, Fukuda T, Tanaka J, Minamitani M, Fujigasaki H, Uchihara T. Neuronal intranuclear hyaline inclusion disease with polyglutamine-immunoreactive inclusions. Acta Neuropathol (Berl) 2000;99:589-594.
-
(2000)
Acta Neuropathol. (Berl.)
, vol.99
, pp. 589-594
-
-
Takahashi, J.1
Fukuda, T.2
Tanaka, J.3
Minamitani, M.4
Fujigasaki, H.5
Uchihara, T.6
-
10
-
-
0018835157
-
An unusual degenerative disorder of neurons associated with a novel intranuclear hyaline inclusion (neuronal intranuclear hyaline inclusion disease). A clinicopathological study of a case
-
Sung JH, Ramirez-Lassepas M, Mastri AR, Larkin SM. An unusual degenerative disorder of neurons associated with a novel intranuclear hyaline inclusion (neuronal intranuclear hyaline inclusion disease). A clinicopathological study of a case. J Neuropathol Exp Neurol 1980;39:107-130.
-
(1980)
J. Neuropathol. Exp. Neurol.
, vol.39
, pp. 107-130
-
-
Sung, J.H.1
Ramirez-Lassepas, M.2
Mastri, A.R.3
Larkin, S.M.4
-
11
-
-
0028267340
-
Neuronal intranuclear hyaline inclusion disease with progressive cerebellar ataxia
-
Sloane AE, Becker LE, Ang LC, Wark J, Haslam RH Neuronal intranuclear hyaline inclusion disease with progressive cerebellar ataxia. Pediatr Neurol 1994;10:61-66.
-
(1994)
Pediatr. Neurol.
, vol.10
, pp. 61-66
-
-
Sloane, A.E.1
Becker, L.E.2
Ang, L.C.3
Wark, J.4
Haslam, R.H.5
-
12
-
-
0025743598
-
Cardiomyopathy and myocyte intranuclear inclusions in Deuronal intranuclear inclusion disease: A case report
-
Oyer CE, Cortez S, O'Shea P, Popovic M. Cardiomyopathy and myocyte intranuclear inclusions in Deuronal intranuclear inclusion disease: a case report. Hum Pathol 1991;22:722-724.
-
(1991)
Hum. Pathol.
, vol.22
, pp. 722-724
-
-
Oyer, C.E.1
Cortez, S.2
O'Shea, P.3
Popovic, M.4
-
13
-
-
0021931663
-
Multiple system atrophy with neuronal intranuclear hyaline inclusions. Report of a case and review of the literature
-
Patel H, Norman MG, Perry TL, Berry KE. Multiple system atrophy with neuronal intranuclear hyaline inclusions. Report of a case and review of the literature. J Neurol Sci 1985;67:57-65.
-
(1985)
J. Neurol. Sci.
, vol.67
, pp. 57-65
-
-
Patel, H.1
Norman, M.G.2
Perry, T.L.3
Berry, K.E.4
-
14
-
-
0021966804
-
Neuronal intranuclear hyaline inclusion disease presenting as Friedreich's ataxia
-
Softer D. Neuronal intranuclear hyaline inclusion disease presenting as Friedreich's ataxia. Acta Neuropathol (Berl) 1985;65:322-329.
-
(1985)
Acta Neuropathol. (Berl.)
, vol.65
, pp. 322-329
-
-
Softer, D.1
-
15
-
-
0019514180
-
Multiple system atrophy with neuronal intranuclear hyaline inclusions. Report of a new case with light and electron microscopic studies
-
Michaud J, Gilbert JJ. Multiple system atrophy with neuronal intranuclear hyaline inclusions. Report of a new case with light and electron microscopic studies. Acta Neuropathol (Berl) 1981;54: 113-119.
-
(1981)
Acta Neuropathol. (Berl.)
, vol.54
, pp. 113-119
-
-
Michaud, J.1
Gilbert, J.J.2
-
16
-
-
0030040502
-
Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case
-
Malandrini A, Fabrizi GM, Cavallaro T, et al. Neuronal intranuclear inclusion disease: polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case. Acta Neuropathol (Berl) 1996;91:215-218.
-
(1996)
Acta Neuropathol. (Berl.)
, vol.91
, pp. 215-218
-
-
Malandrini, A.1
Fabrizi, G.M.2
Cavallaro, T.3
-
17
-
-
0023518669
-
Neuronal intranuclear hyaline inclusion disease associated with premature coronary atherosclerosis
-
Parker JC Jr, Dyer ML, Paulsen WA. Neuronal intranuclear hyaline inclusion disease associated with premature coronary atherosclerosis. J Clin Neuroophthalmol 1987;7:244-249.
-
(1987)
J. Clin. Neuroophthalmol.
, vol.7
, pp. 244-249
-
-
Parker Jr., J.C.1
Dyer, M.L.2
Paulsen, W.A.3
-
18
-
-
0018142835
-
A familial neuronal disease presenting as intestinal pseudoobstruction
-
Schuffler MD, Bird TD, Sumi SM, Cook A. A familial neuronal disease presenting as intestinal pseudoobstruction. Gastroenterology 1978;75:889-898.
-
(1978)
Gastroenterology
, vol.75
, pp. 889-898
-
-
Schuffler, M.D.1
Bird, T.D.2
Sumi, S.M.3
Cook, A.4
-
19
-
-
0021319550
-
Intranuclear inclusions in muscle, nervous tissue, and adrenal gland
-
Tateishi J, Nagara H, Ohta M, Matsumoto T, Fukunaga H, Shida K. Intranuclear inclusions in muscle, nervous tissue, and adrenal gland. Acta Neuropathol (Berl) 1984;63:24-32.
-
(1984)
Acta Neuropathol. (Berl.)
, vol.63
, pp. 24-32
-
-
Tateishi, J.1
Nagara, H.2
Ohta, M.3
Matsumoto, T.4
Fukunaga, H.5
Shida, K.6
-
20
-
-
0028919786
-
Intranuclear inclusion bodies in an elderly demented woman: A form of intranuclear inclusion body disease
-
Weidenheim KM, Dickson DW. Intranuclear inclusion bodies in an elderly demented woman: a form of intranuclear inclusion body disease. Clin Neuropathol 1995;14:93-99.
-
(1995)
Clin. Neuropathol.
, vol.14
, pp. 93-99
-
-
Weidenheim, K.M.1
Dickson, D.W.2
-
21
-
-
0026566877
-
Familial visceral neuropathy with neuronal intranuclear inclusions: Diagnosis by rectal biopsy
-
Barnett JL, McDonnell WM, Appelman HD, Dobbins WO. Familial visceral neuropathy with neuronal intranuclear inclusions: diagnosis by rectal biopsy. Gastroenterology 1992;102:684-691.
-
(1992)
Gastroenterology
, vol.102
, pp. 684-691
-
-
Barnett, J.L.1
McDonnell, W.M.2
Appelman, H.D.3
Dobbins, W.O.4
-
22
-
-
0023898945
-
The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
-
Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988;51:745-752.
-
(1988)
J. Neurol. Neurosurg. Psychiatry
, vol.51
, pp. 745-752
-
-
Gibb, W.R.1
Lees, A.J.2
-
23
-
-
0033809402
-
Neuronal intranuclear inclusion disease and juvenile parkinsonism
-
O'Sullivan JD, Hanagasi HA, Daniel SE, Tidswell P, Davies SW, Lees AJ. Neuronal intranuclear inclusion disease and juvenile parkinsonism. Mov Disord 2000;15:990-995.
-
(2000)
Mov. Disord.
, vol.15
, pp. 990-995
-
-
O'Sullivan, J.D.1
Hanagasi, H.A.2
Daniel, S.E.3
Tidswell, P.4
Davies, S.W.5
Lees, A.J.6
-
24
-
-
0346216846
-
Neuronal intranuclear hyaline inclusion disease
-
Takahashi-Fujigasaki J. Neuronal intranuclear hyaline inclusion disease. Neuropathology 2003;23:351-359.
-
(2003)
Neuropathology
, vol.23
, pp. 351-359
-
-
Takahashi-Fujigasaki, J.1
-
25
-
-
0023784368
-
A comparison of clinical and pathological features of young- and old-onset Parkinson's disease
-
Gibb WR, Lees AJ. A comparison of clinical and pathological features of young- and old-onset Parkinson's disease. Neurology 1988;38:1402-1406.
-
(1988)
Neurology
, vol.38
, pp. 1402-1406
-
-
Gibb, W.R.1
Lees, A.J.2
-
26
-
-
0342368772
-
Association between early-onset Parkinson's disease and mutations in the parkin gene
-
French Parkinson's Disease Genetics Study Group
-
Lucking CB, Durr A, Bonifati V, et at. Association between early-onset Parkinson's disease and mutations in the parkin gene. French Parkinson's Disease Genetics Study Group. N Engl J Med 2000;342:1560-1567.
-
(2000)
N. Engl. J. Med.
, vol.342
, pp. 1560-1567
-
-
Lucking, C.B.1
Durr, A.2
Bonifati, V.3
-
27
-
-
1542300954
-
Diagnostic considerations in juvenile parkinsonism
-
Paviour DC, Surtees RA, Lees AJ. Diagnostic considerations in juvenile parkinsonism. Mov Disord 2004;19:123-135.
-
(2004)
Mov. Disord.
, vol.19
, pp. 123-135
-
-
Paviour, D.C.1
Surtees, R.A.2
Lees, A.J.3
-
28
-
-
0026456574
-
Dopa-responsive dystonia with depigmentation of the substantia nigra and formation of Lewy bodies
-
Olsson JE, Brunk U, Lindvall B, Eeg-Olofsson O. Dopa-responsive dystonia with depigmentation of the substantia nigra and formation of Lewy bodies. J Neurol Sci 1992; 112:90 -95.
-
(1992)
J. Neurol. Sci.
, vol.112
, pp. 90-95
-
-
Olsson, J.E.1
Brunk, U.2
Lindvall, B.3
Eeg-Olofsson, O.4
-
30
-
-
0345206165
-
Dopa responsive dystonia (DRD) presenting in the first year of life
-
Bebin EM, Fryburg JS, Trugman JM. Dopa responsive dystonia (DRD) presenting in the first year of life. Neurology 1995; 45(Suppl):184.
-
(1995)
Neurology
, vol.45
, Issue.SUPPL.
, pp. 184
-
-
Bebin, E.M.1
Fryburg, J.S.2
Trugman, J.M.3
-
31
-
-
0023518669
-
Neuronal intranuclear hyaline inclusion disease associated with premature coronary atherosclerosis
-
Parker JC Jr, Dyer ML, Paulsen WA. Neuronal intranuclear hyaline inclusion disease associated with premature coronary atherosclerosis. J Clin Neuroophthalmol 1987;7:244-249.
-
(1987)
J. Clin. Neuroophthalmol.
, vol.7
, pp. 244-249
-
-
Parker Jr., J.C.1
Dyer, M.L.2
Paulsen, W.A.3
-
33
-
-
0027354029
-
Dopa-responsive dystonia. Delineation of the clinical syndrome and clues to pathogenesis
-
Nygaard TG. Dopa-responsive dystonia. Delineation of the clinical syndrome and clues to pathogenesis. Adv Neurol 1993;60:577-585.
-
(1993)
Adv. Neurol.
, vol.60
, pp. 577-585
-
-
Nygaard, T.G.1
-
34
-
-
0028221755
-
Dopa-responsive dystonia: Pathological and biochemical observations in a case
-
Rajput AH, Gibb WR, Zhong XH, et al. Dopa-responsive dystonia: pathological and biochemical observations in a case. Ann Neurol 1994;35:396-402.
-
(1994)
Ann. Neurol.
, vol.35
, pp. 396-402
-
-
Rajput, A.H.1
Gibb, W.R.2
Zhong, X.H.3
-
35
-
-
0037172668
-
Neuropathology of a case of dopa-responsive dystonia associated with a new genetic locus, DYT14
-
Grotzsch H, Pizzolato GP, Ghika J, et al. Neuropathology of a case of dopa-responsive dystonia associated with a new genetic locus, DYT14. Neurology 2002;58:1839-1842.
-
(2002)
Neurology
, vol.58
, pp. 1839-1842
-
-
Grotzsch, H.1
Pizzolato, G.P.2
Ghika, J.3
-
36
-
-
0036225503
-
Brain biopterin and tyrosine hydroxylase in asymptomatic dopa-responsive dystonia
-
Furukawa Y, Kapatos G, Haycock JW, et al. Brain biopterin and tyrosine hydroxylase in asymptomatic dopa-responsive dystonia. Ann Neurol 2002;51:637-641.
-
(2002)
Ann. Neurol.
, vol.51
, pp. 637-641
-
-
Furukawa, Y.1
Kapatos, G.2
Haycock, J.W.3
-
37
-
-
0036345801
-
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
-
Greco CM, Hagerman RJ, Tassone F, et al. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain 2002;125:1760-1771.
-
(2002)
Brain
, vol.125
, pp. 1760-1771
-
-
Greco, C.M.1
Hagerman, R.J.2
Tassone, F.3
-
38
-
-
0037102710
-
Intranuclear inclusions, neuronal loss and CAG mosaicism in two patients with Machado-Joseph disease
-
Munoz E, Rey MJ, Mila M, et al. Intranuclear inclusions, neuronal loss and CAG mosaicism in two patients with Machado-Joseph disease. J Neurol Sci 2002;200:19-25.
-
(2002)
J. Neurol. Sci.
, vol.200
, pp. 19-25
-
-
Munoz, E.1
Rey, M.J.2
Mila, M.3
-
39
-
-
7144229376
-
Spinocerebellar ataxia type 7 (SCA7): A neurodegenerative disorder with neuronal intranuclear inclusions
-
Holmberg M, Duyckaerts C, Durr A, et al. Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions. Hum Mot Genet 1998;7:913-918.
-
(1998)
Hum. Mot. Genet.
, vol.7
, pp. 913-918
-
-
Holmberg, M.1
Duyckaerts, C.2
Durr, A.3
-
40
-
-
0030040304
-
Spinocerebellar ataxia type I with multiple system degeneration and glial cytoplasmic inclusions
-
Gilman S, Sima AA, Junck L, et al. Spinocerebellar ataxia type I with multiple system degeneration and glial cytoplasmic inclusions. Ann Neurol 1996;39:241-255.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 241-255
-
-
Gilman, S.1
Sima, A.A.2
Junck, L.3
-
41
-
-
0036185711
-
Neuronal intranuclear inclusions in SCA2: A genetic, morphological and immunohistochemical study of two cases
-
Pang JT, Giund P, Chamberlain S, et al. Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases, Brain 2002;125:656-663.
-
(2002)
Brain
, vol.125
, pp. 656-663
-
-
Pang, J.T.1
Giund, P.2
Chamberlain, S.3
-
42
-
-
0031655821
-
Intranuclear neuronal inclusions in DR-PLA
-
Becher MW, Ross CA. Intranuclear neuronal inclusions in DR-PLA. Mov Disord 1998;13:852-853.
-
(1998)
Mov. Disord.
, vol.13
, pp. 852-853
-
-
Becher, M.W.1
Ross, C.A.2
-
43
-
-
0031918640
-
Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: Correlation between the density of inclusions and IT15 CAG triplet repeat length
-
Becher MW, Kotzuk JA, Sharp AH et al. Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length. Neurobiol Dis 1998; 4:387-397.
-
(1998)
Neurobiol. Dis.
, vol.4
, pp. 387-397
-
-
Becher, M.W.1
Kotzuk, J.A.2
Sharp, A.H.3
-
44
-
-
0037046199
-
Autosomal dominant chorea-acanthocytosis with polyglutamine-containing neuronal inclusions
-
Walker RH, Morgello S, Davidoff-Feldman B, et al. Autosomal dominant chorea-acanthocytosis with polyglutamine-containing neuronal inclusions. Neurology 2002;58:1031-1037.
-
(2002)
Neurology
, vol.58
, pp. 1031-1037
-
-
Walker, R.H.1
Morgello, S.2
Davidoff-Feldman, B.3
-
45
-
-
0032837943
-
Ataxin I and ataxin 3 in neuronal intranuclear inclusion disease
-
Lieberman AP, Trojanowski JQ Leonard DG, et al. Ataxin I and ataxin 3 in neuronal intranuclear inclusion disease. Ann Neurol 1999;46:271-273.
-
(1999)
Ann. Neurol.
, vol.46
, pp. 271-273
-
-
Lieberman, A.P.1
Trojanowski, J.Q.2
Leonard, D.G.3
-
46
-
-
0028972448
-
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
-
Trottier Y, Lutz Y, Stevanin G, et al. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature 1995;378:403-406.
-
(1995)
Nature
, vol.378
, pp. 403-406
-
-
Trottier, Y.1
Lutz, Y.2
Stevanin, G.3
-
47
-
-
0032554551
-
Polyglutamine-containing aggregates in neuronal intranuclear inclusion disease
-
Lieberman AP, Robitaille Y, Trojanowski JQ Dickson DW, Fischbeck KH. Polyglutamine-containing aggregates in neuronal intranuclear inclusion disease. Lancet 1998;351:884.
-
(1998)
Lancet
, vol.351
, pp. 884
-
-
Lieberman, A.P.1
Robitaille, Y.2
Trojanowski, J.Q.3
Dickson, D.W.4
Fischbeck, K.H.5
-
48
-
-
0035060505
-
Recruitment of nonexpanded polyglutamine proteins to intranuclear aggregates in neuronal intranuclear hyaline inclusion disease
-
Takahashi J, Tanaka J, Arai K, et al. Recruitment of nonexpanded polyglutamine proteins to intranuclear aggregates in neuronal intranuclear hyaline inclusion disease. J Neuropathol Exp Neurol 2001;60:369-376.
-
(2001)
J. Neuropathol. Exp. Neurol.
, vol.60
, pp. 369-376
-
-
Takahashi, J.1
Tanaka, J.2
Arai, K.3
|