-
1
-
-
84865839732
-
Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management
-
Seltman R.E., Matthews B.R. Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management. CNS Drug 2012, 26:841-870.
-
(2012)
CNS Drug
, vol.26
, pp. 841-870
-
-
Seltman, R.E.1
Matthews, B.R.2
-
2
-
-
0036205905
-
Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene
-
Pickering-Brown S.M., et al. Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. Brain 2002, 125:732-751.
-
(2002)
Brain
, vol.125
, pp. 732-751
-
-
Pickering-Brown, S.M.1
-
3
-
-
34547663747
-
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions
-
Cairns N.J., et al. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am. J. Pathol. 2007, 171:227-240.
-
(2007)
Am. J. Pathol.
, vol.171
, pp. 227-240
-
-
Cairns, N.J.1
-
4
-
-
79451472241
-
Distinct pathological subtypes of FTLD-FUS
-
Mackenzie I.R., et al. Distinct pathological subtypes of FTLD-FUS. Acta Neuropathol. 2011, 121:207-218.
-
(2011)
Acta Neuropathol.
, vol.121
, pp. 207-218
-
-
Mackenzie, I.R.1
-
5
-
-
79958098783
-
TDP-43 in aging and Alzheimer's disease - a review
-
Wilson A.C., et al. TDP-43 in aging and Alzheimer's disease - a review. Int. J. Clin. Exp. Pathol. 2011, 4:147-155.
-
(2011)
Int. J. Clin. Exp. Pathol.
, vol.4
, pp. 147-155
-
-
Wilson, A.C.1
-
6
-
-
70350673956
-
A new subtype of frontotemporal lobar degeneration with FUS pathology
-
Neumann M., et al. A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain 2009, 132:2922-2931.
-
(2009)
Brain
, vol.132
, pp. 2922-2931
-
-
Neumann, M.1
-
7
-
-
84865862939
-
The genetics and neuropathology of frontotemporal lobar degeneration
-
Sieben A., et al. The genetics and neuropathology of frontotemporal lobar degeneration. Acta Neuropathol. 2012, 124:353-372.
-
(2012)
Acta Neuropathol.
, vol.124
, pp. 353-372
-
-
Sieben, A.1
-
8
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
Baker M., et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 2006, 442:916-919.
-
(2006)
Nature
, vol.442
, pp. 916-919
-
-
Baker, M.1
-
9
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
-
Cruts M., et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 2006, 442:920-924.
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
-
10
-
-
76149123541
-
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration
-
Yu C.E., et al. The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. Arch. Neurol. 2010, 67:161-170.
-
(2010)
Arch. Neurol.
, vol.67
, pp. 161-170
-
-
Yu, C.E.1
-
11
-
-
55549141535
-
Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family
-
Chiang H.H., et al. Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family. Alzheimers Dement. 2008, 4:414-420.
-
(2008)
Alzheimers Dement.
, vol.4
, pp. 414-420
-
-
Chiang, H.H.1
-
12
-
-
42049108445
-
Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
-
Mukherjee O., et al. Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia. Hum. Mutat. 2008, 29:512-521.
-
(2008)
Hum. Mutat.
, vol.29
, pp. 512-521
-
-
Mukherjee, O.1
-
13
-
-
84862134180
-
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage
-
Smith K.R., et al. Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage. Am. J. Hum. Genet. 2012, 90:1102-1107.
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 1102-1107
-
-
Smith, K.R.1
-
14
-
-
79953883507
-
Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
-
Seelaar H., et al. Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review. J. Neurol. Neurosurg. Psychiatry 2011, 82:476-486.
-
(2011)
J. Neurol. Neurosurg. Psychiatry
, vol.82
, pp. 476-486
-
-
Seelaar, H.1
-
15
-
-
84863461863
-
Clinical phenotypes and genetic biomarkers of FTLD
-
Galimberti D., Scarpini E. Clinical phenotypes and genetic biomarkers of FTLD. J. Neural Transm. 2012, 119:851-860.
-
(2012)
J. Neural Transm.
, vol.119
, pp. 851-860
-
-
Galimberti, D.1
Scarpini, E.2
-
16
-
-
84870535861
-
Recent advances in the imaging of frontotemporal dementia
-
Whitwell J.L., Josephs K.A. Recent advances in the imaging of frontotemporal dementia. Curr. Neurol. Neurosci. Rep. 2012, 12:715-723.
-
(2012)
Curr. Neurol. Neurosci. Rep.
, vol.12
, pp. 715-723
-
-
Whitwell, J.L.1
Josephs, K.A.2
-
17
-
-
84872467136
-
Structural brain signature of FTLD driven by Granulin mutation
-
Bozzali M., et al. Structural brain signature of FTLD driven by Granulin mutation. J. Alzheimers Dis. 2013, 33:483-494.
-
(2013)
J. Alzheimers Dis.
, vol.33
, pp. 483-494
-
-
Bozzali, M.1
-
18
-
-
62849095858
-
Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN
-
Whitwell J.L., et al. Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN. Neurology 2009, 72:813-820.
-
(2009)
Neurology
, vol.72
, pp. 813-820
-
-
Whitwell, J.L.1
-
19
-
-
79959599081
-
A harmonized classification system for FTLD-TDP pathology
-
Mackenzie I.R., et al. A harmonized classification system for FTLD-TDP pathology. Acta Neuropathol. 2011, 122:111-113.
-
(2011)
Acta Neuropathol.
, vol.122
, pp. 111-113
-
-
Mackenzie, I.R.1
-
20
-
-
33846794448
-
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations
-
Josephs K.A., et al. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations. J. Neuropathol. Exp. Neurol. 2007, 66:142-151.
-
(2007)
J. Neuropathol. Exp. Neurol.
, vol.66
, pp. 142-151
-
-
Josephs, K.A.1
-
21
-
-
41949132982
-
TAR DNA-binding protein 43 immunohistochemistry reveals extensive neuritic pathology in FTLD-U: a midwest-southwest consortium for FTLD study
-
Hatanpaa K.J., et al. TAR DNA-binding protein 43 immunohistochemistry reveals extensive neuritic pathology in FTLD-U: a midwest-southwest consortium for FTLD study. J. Neuropathol. Exp. Neurol. 2008, 67:271-279.
-
(2008)
J. Neuropathol. Exp. Neurol.
, vol.67
, pp. 271-279
-
-
Hatanpaa, K.J.1
-
22
-
-
78651268247
-
A morphometric study of the spatial patterns of TDP-43 immunoreactive neuronal inclusions in frontotemporal lobar degeneration (FTLD) with progranulin (GRN) mutation
-
Armstrong R.A., Cairns N.J. A morphometric study of the spatial patterns of TDP-43 immunoreactive neuronal inclusions in frontotemporal lobar degeneration (FTLD) with progranulin (GRN) mutation. Histol. Histopathol. 2011, 26:185-190.
-
(2011)
Histol. Histopathol.
, vol.26
, pp. 185-190
-
-
Armstrong, R.A.1
Cairns, N.J.2
-
23
-
-
77952496156
-
Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation
-
Gliebus G., et al. Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation. Neurology 2010, 74:1607-1610.
-
(2010)
Neurology
, vol.74
, pp. 1607-1610
-
-
Gliebus, G.1
-
24
-
-
84980053522
-
Circulating progranulin as a biomarker for neurodegenerative diseases
-
Ghidoni R., et al. Circulating progranulin as a biomarker for neurodegenerative diseases. Am. J. Neurodegener. Dis. 2012, 1:180-190.
-
(2012)
Am. J. Neurodegener. Dis.
, vol.1
, pp. 180-190
-
-
Ghidoni, R.1
-
25
-
-
79551543554
-
Rescue of progranulin deficiency associated with frontotemporal lobar degeneration by alkalizing reagents and inhibition of vacuolar ATPase
-
Capell A., et al. Rescue of progranulin deficiency associated with frontotemporal lobar degeneration by alkalizing reagents and inhibition of vacuolar ATPase. J. Neurosci. 2011, 31:1885-1894.
-
(2011)
J. Neurosci.
, vol.31
, pp. 1885-1894
-
-
Capell, A.1
-
26
-
-
79955534069
-
Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia
-
Cenik B., et al. Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia. J. Biol. Chem. 2011, 286:16101-16108.
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 16101-16108
-
-
Cenik, B.1
-
27
-
-
84875367680
-
Frontotemporal degeneration, the next therapeutic frontier: molecules and animal models for frontotemporal degeneration drug development
-
Boxer A.L., et al. Frontotemporal degeneration, the next therapeutic frontier: molecules and animal models for frontotemporal degeneration drug development. Alzheimers Dement. 2013, 9:176-188.
-
(2013)
Alzheimers Dement.
, vol.9
, pp. 176-188
-
-
Boxer, A.L.1
-
28
-
-
33749568019
-
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
-
Gass J., et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum. Mol. Genet. 2006, 15:2988-3001.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 2988-3001
-
-
Gass, J.1
-
29
-
-
34548633862
-
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative
-
Rademakers R., et al. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Lancet Neurol. 2007, 6:857-868.
-
(2007)
Lancet Neurol.
, vol.6
, pp. 857-868
-
-
Rademakers, R.1
-
30
-
-
84860719745
-
Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin
-
McDade E., et al. Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin. Neurology 2012, 78:1245-1249.
-
(2012)
Neurology
, vol.78
, pp. 1245-1249
-
-
McDade, E.1
-
31
-
-
77649136250
-
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
-
Van Deerlin V.M., et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat. Genet. 2010, 42:234-239.
-
(2010)
Nat. Genet.
, vol.42
, pp. 234-239
-
-
Van Deerlin, V.M.1
-
32
-
-
84861722031
-
Membrane orientation and subcellular localization of transmembrane protein 106B (TMEM106B), a major risk factor for frontotemporal lobar degeneration
-
Lang C.M., et al. Membrane orientation and subcellular localization of transmembrane protein 106B (TMEM106B), a major risk factor for frontotemporal lobar degeneration. J. Biol. Chem. 2012, 287:19355-19365.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 19355-19365
-
-
Lang, C.M.1
-
33
-
-
84865008239
-
TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways
-
Chen-Plotkin A.S., et al. TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways. J. Neurosci. 2012, 32:11213-11227.
-
(2012)
J. Neurosci.
, vol.32
, pp. 11213-11227
-
-
Chen-Plotkin, A.S.1
-
34
-
-
79951494607
-
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
-
Finch N., et al. TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers. Neurology 2010, 76:467-474.
-
(2010)
Neurology
, vol.76
, pp. 467-474
-
-
Finch, N.1
-
35
-
-
79952148055
-
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
-
van der Zee J., et al. TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. Brain 2011, 134:808-815.
-
(2011)
Brain
, vol.134
, pp. 808-815
-
-
van der Zee, J.1
-
36
-
-
79955748378
-
Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels
-
Cruchaga C., et al. Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels. Arch. Neurol. 2011, 68:581-586.
-
(2011)
Arch. Neurol.
, vol.68
, pp. 581-586
-
-
Cruchaga, C.1
-
37
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
DeJesus-Hernandez M., et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011, 72:245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
-
38
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
Renton A.E., et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011, 72:257-268.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
-
39
-
-
84888235194
-
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
-
van Blitterswijk M., et al. C9ORF72 repeat expansions in cases with previously identified pathogenic mutations. Neurology 2013, 81:1332-1341.
-
(2013)
Neurology
, vol.81
, pp. 1332-1341
-
-
van Blitterswijk, M.1
-
40
-
-
84896708010
-
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia
-
Lashley T., et al. A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia. Neuropathol. Appl. Neurobiol. 2013, 10.1111/nan.12100.
-
(2013)
Neuropathol. Appl. Neurobiol.
-
-
Lashley, T.1
-
41
-
-
79955952980
-
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort
-
Del Bo R., et al. No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Neurobiol. Aging 2011, 32:1157-1158.
-
(2011)
Neurobiol. Aging
, vol.32
, pp. 1157-1158
-
-
Del Bo, R.1
-
42
-
-
34347245619
-
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes
-
Schymick J.C., et al. Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes. J. Neurol. Neurosurg. Psychiatry 2007, 78:754-756.
-
(2007)
J. Neurol. Neurosurg. Psychiatry
, vol.78
, pp. 754-756
-
-
Schymick, J.C.1
-
43
-
-
55249086715
-
Progranulin variability has no major role in Parkinson disease genetic etiology
-
Nuytemans K., et al. Progranulin variability has no major role in Parkinson disease genetic etiology. Neurology 2008, 71:1147-1151.
-
(2008)
Neurology
, vol.71
, pp. 1147-1151
-
-
Nuytemans, K.1
-
44
-
-
52449110477
-
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
-
Brouwers N., et al. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology 2008, 71:656-664.
-
(2008)
Neurology
, vol.71
, pp. 656-664
-
-
Brouwers, N.1
-
45
-
-
84980052138
-
C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic
-
Wojtas A., et al. C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic. Am. J. Neurodegener. Dis. 2012, 1:107-118.
-
(2012)
Am. J. Neurodegener. Dis.
, vol.1
, pp. 107-118
-
-
Wojtas, A.1
-
46
-
-
35348872039
-
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
-
Brouwers N., et al. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. Arch. Neurol. 2007, 64:1436-1446.
-
(2007)
Arch. Neurol.
, vol.64
, pp. 1436-1446
-
-
Brouwers, N.1
-
47
-
-
76149131323
-
Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin
-
Kelley B.J., et al. Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin. Arch. Neurol. 2010, 67:171-177.
-
(2010)
Arch. Neurol.
, vol.67
, pp. 171-177
-
-
Kelley, B.J.1
-
48
-
-
84879092067
-
Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis
-
Cannon A., et al. Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis. Neurology 2013, 80:1771-1777.
-
(2013)
Neurology
, vol.80
, pp. 1771-1777
-
-
Cannon, A.1
-
49
-
-
84878797585
-
Progranulin mutations as risk factors for Alzheimer disease
-
Perry D.C., et al. Progranulin mutations as risk factors for Alzheimer disease. JAMA Neurol. 2013, 70:1-5.
-
(2013)
JAMA Neurol.
, vol.70
, pp. 1-5
-
-
Perry, D.C.1
-
50
-
-
75149197665
-
GRN variability contributes to sporadic frontotemporal lobar degeneration
-
Galimberti D., et al. GRN variability contributes to sporadic frontotemporal lobar degeneration. J. Alzheimers Dis. 2010, 19:171-177.
-
(2010)
J. Alzheimers Dis.
, vol.19
, pp. 171-177
-
-
Galimberti, D.1
-
51
-
-
84879114551
-
Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration
-
Galimberti D., et al. Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration. Neurol. Sci. 2012, 34:899-903.
-
(2012)
Neurol. Sci.
, vol.34
, pp. 899-903
-
-
Galimberti, D.1
-
52
-
-
56049083010
-
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
-
Rademakers R., et al. Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia. Hum. Mol. Genet. 2008, 17:3631-3642.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3631-3642
-
-
Rademakers, R.1
-
53
-
-
79953058497
-
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration
-
Rollinson S., et al. No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration. Neurobiol. Aging 2011, 32:754-755.
-
(2011)
Neurobiol. Aging
, vol.32
, pp. 754-755
-
-
Rollinson, S.1
-
54
-
-
78650511054
-
Rs5848 polymorphism and serum progranulin level
-
Hsiung G.Y., et al. rs5848 polymorphism and serum progranulin level. J. Neurol. Sci. 2011, 300(1-2):28-32.
-
(2011)
J. Neurol. Sci.
, vol.300
, Issue.1-2
, pp. 28-32
-
-
Hsiung, G.Y.1
-
55
-
-
84872442945
-
GRN variant rs5848 reduces plasma and brain levels of granulin in Alzheimer's disease patients
-
Kamalainen A., et al. GRN variant rs5848 reduces plasma and brain levels of granulin in Alzheimer's disease patients. J. Alzheimers Dis. 2013, 33:23-27.
-
(2013)
J. Alzheimers Dis.
, vol.33
, pp. 23-27
-
-
Kamalainen, A.1
-
56
-
-
77449111778
-
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly
-
Dickson D.W., et al. Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. Neurodegener. Dis. 2010, 7(1-3):170-174.
-
(2010)
Neurodegener. Dis.
, vol.7
, Issue.1-3
, pp. 170-174
-
-
Dickson, D.W.1
-
57
-
-
81855175349
-
Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically
-
Pao W.C., et al. Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically. Alzheimer Dis. Assoc. Disord. 2011, 25:364-368.
-
(2011)
Alzheimer Dis. Assoc. Disord.
, vol.25
, pp. 364-368
-
-
Pao, W.C.1
-
58
-
-
42049120518
-
Progranulin genetic variability contributes to amyotrophic lateral sclerosis
-
Sleegers K., et al. Progranulin genetic variability contributes to amyotrophic lateral sclerosis. Neurology 2008, 71:253-259.
-
(2008)
Neurology
, vol.71
, pp. 253-259
-
-
Sleegers, K.1
-
59
-
-
75149192605
-
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease
-
Fenoglio C., et al. Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease. J. Alzheimers Dis. 2009, 18:603-612.
-
(2009)
J. Alzheimers Dis.
, vol.18
, pp. 603-612
-
-
Fenoglio, C.1
-
60
-
-
79955830791
-
Rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population
-
Lee M.J., et al. rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population. Neurodegener. Dis. 2011, 8:216-220.
-
(2011)
Neurodegener. Dis.
, vol.8
, pp. 216-220
-
-
Lee, M.J.1
-
61
-
-
77956342941
-
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males
-
Fenoglio C., et al. Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males. Genes Immun. 2010, 11:497-503.
-
(2010)
Genes Immun.
, vol.11
, pp. 497-503
-
-
Fenoglio, C.1
-
62
-
-
77952921864
-
Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia
-
Momeni P., et al. Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia. Neurocase 2010, 16:273-279.
-
(2010)
Neurocase
, vol.16
, pp. 273-279
-
-
Momeni, P.1
-
63
-
-
77955707871
-
Progranulin expression in the developing and adult murine brain
-
Petkau T.L., et al. Progranulin expression in the developing and adult murine brain. J. Comp. Neurol. 2010, 518:3931-3947.
-
(2010)
J. Comp. Neurol.
, vol.518
, pp. 3931-3947
-
-
Petkau, T.L.1
-
64
-
-
79952909682
-
Age-dependent changes in progranulin expression in the mouse brain
-
Matsuwaki T., et al. Age-dependent changes in progranulin expression in the mouse brain. J. Reprod. Dev. 2010, 57:113-119.
-
(2010)
J. Reprod. Dev.
, vol.57
, pp. 113-119
-
-
Matsuwaki, T.1
-
65
-
-
77954578417
-
Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful aging
-
Ahmed Z., et al. Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful aging. Am. J. Pathol. 2010, 177:311-324.
-
(2010)
Am. J. Pathol.
, vol.177
, pp. 311-324
-
-
Ahmed, Z.1
-
66
-
-
80053540582
-
Delayed inflammatory mRNA and protein expression after spinal cord injury
-
Byrnes K.R., et al. Delayed inflammatory mRNA and protein expression after spinal cord injury. J. Neuroinflammation 2011, 8:130.
-
(2011)
J. Neuroinflammation
, vol.8
, pp. 130
-
-
Byrnes, K.R.1
-
67
-
-
77649192710
-
Progranulin expression is upregulated after spinal contusion in mice
-
Naphade S.B., et al. Progranulin expression is upregulated after spinal contusion in mice. Acta Neuropathol. 2010, 119:123-133.
-
(2010)
Acta Neuropathol.
, vol.119
, pp. 123-133
-
-
Naphade, S.B.1
-
68
-
-
58049221032
-
Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: implications for TDP-43 in the physiological response to neuronal injury
-
Moisse K., et al. Divergent patterns of cytosolic TDP-43 and neuronal progranulin expression following axotomy: implications for TDP-43 in the physiological response to neuronal injury. Brain Res. 2009, 1249:202-211.
-
(2009)
Brain Res.
, vol.1249
, pp. 202-211
-
-
Moisse, K.1
-
69
-
-
84871778200
-
Exacerbated inflammatory responses related to activated microglia after traumatic brain injury in progranulin-deficient mice
-
Tanaka Y., et al. Exacerbated inflammatory responses related to activated microglia after traumatic brain injury in progranulin-deficient mice. Neuroscience 2013, 231:49-60.
-
(2013)
Neuroscience
, vol.231
, pp. 49-60
-
-
Tanaka, Y.1
-
70
-
-
58149147341
-
Progranulin (PGRN) expression in ALS: an immunohistochemical study
-
Irwin D., et al. Progranulin (PGRN) expression in ALS: an immunohistochemical study. J. Neurol. Sci. 2009, 276(1-2):9-13.
-
(2009)
J. Neurol. Sci.
, vol.276
, Issue.1-2
, pp. 9-13
-
-
Irwin, D.1
-
71
-
-
0035085455
-
Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays
-
Malaspina A., et al. Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays. J. Neurochem. 2001, 77:132-145.
-
(2001)
J. Neurochem.
, vol.77
, pp. 132-145
-
-
Malaspina, A.1
-
72
-
-
78650178041
-
Microglial upregulation of progranulin as a marker of motor neuron degeneration
-
Philips T., et al. Microglial upregulation of progranulin as a marker of motor neuron degeneration. J. Neuropathol. Exp. Neurol. 2010, 69:1191-1200.
-
(2010)
J. Neuropathol. Exp. Neurol.
, vol.69
, pp. 1191-1200
-
-
Philips, T.1
-
73
-
-
54049135189
-
Association between progranulin and beta-amyloid in dementia with Lewy bodies
-
Revuelta G.J., et al. Association between progranulin and beta-amyloid in dementia with Lewy bodies. Am. J. Alzheimers Dis. Other Demen. 2008, 23:488-493.
-
(2008)
Am. J. Alzheimers Dis. Other Demen.
, vol.23
, pp. 488-493
-
-
Revuelta, G.J.1
-
74
-
-
70450284414
-
Progranulin and beta-amyloid distribution: a case report of the brain from preclinical PS-1 mutation carrier
-
Gliebus G., et al. Progranulin and beta-amyloid distribution: a case report of the brain from preclinical PS-1 mutation carrier. Am. J. Alzheimers Dis. Other Demen. 2009, 24:456-460.
-
(2009)
Am. J. Alzheimers Dis. Other Demen.
, vol.24
, pp. 456-460
-
-
Gliebus, G.1
-
75
-
-
70349091081
-
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models
-
Pereson S., et al. Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models. J. Pathol. 2009, 219:173-181.
-
(2009)
J. Pathol.
, vol.219
, pp. 173-181
-
-
Pereson, S.1
-
76
-
-
80053226483
-
Progranulin expression in brain tissue and cerebrospinal fluid levels in multiple sclerosis
-
Vercellino M., et al. Progranulin expression in brain tissue and cerebrospinal fluid levels in multiple sclerosis. Mult. Scler. 2011, 17:1194-1201.
-
(2011)
Mult. Scler.
, vol.17
, pp. 1194-1201
-
-
Vercellino, M.1
-
77
-
-
77649192195
-
Brain progranulin expression in GRN-associated frontotemporal lobar degeneration
-
Chen-Plotkin A.S., et al. Brain progranulin expression in GRN-associated frontotemporal lobar degeneration. Acta Neuropathol. 2010, 119:111-122.
-
(2010)
Acta Neuropathol.
, vol.119
, pp. 111-122
-
-
Chen-Plotkin, A.S.1
-
78
-
-
84867996771
-
Progranulin overexpression predicts overall survival in patients with glioblastoma
-
Wang M., et al. Progranulin overexpression predicts overall survival in patients with glioblastoma. Med. Oncol. 2012, 29:2423-2431.
-
(2012)
Med. Oncol.
, vol.29
, pp. 2423-2431
-
-
Wang, M.1
-
79
-
-
80855131487
-
Structure, function, and mechanism of progranulin; the brain and beyond
-
Toh H., et al. Structure, function, and mechanism of progranulin; the brain and beyond. J. Mol. Neurosci. 2011, 45:538-548.
-
(2011)
J. Mol. Neurosci.
, vol.45
, pp. 538-548
-
-
Toh, H.1
-
80
-
-
84859590507
-
Regulation of progranulin expression in human microglia and proteolysis of progranulin by matrix metalloproteinase-12 (MMP-12)
-
Suh H.S., et al. Regulation of progranulin expression in human microglia and proteolysis of progranulin by matrix metalloproteinase-12 (MMP-12). PLoS ONE 2012, 7:e35115. 10.1371/journal.pone.0035115.
-
(2012)
PLoS ONE
, vol.7
-
-
Suh, H.S.1
-
81
-
-
77957818067
-
Progranulin modulates zebrafish motoneuron development in vivo and rescues truncation defects associated with knockdown of Survival motor neuron 1
-
Chitramuthu B.P., et al. Progranulin modulates zebrafish motoneuron development in vivo and rescues truncation defects associated with knockdown of Survival motor neuron 1. Mol. Neurodegener. 2010, 5:41.
-
(2010)
Mol. Neurodegener.
, vol.5
, pp. 41
-
-
Chitramuthu, B.P.1
-
82
-
-
78149429744
-
Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy
-
Laird A.S., et al. Progranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathy. PLoS ONE 2010, 5:e13368. 10.1371/journal.pone.0013368.
-
(2010)
PLoS ONE
, vol.5
-
-
Laird, A.S.1
-
83
-
-
70749120467
-
Progranulin is expressed within motor neurons and promotes neuronal cell survival
-
Ryan C.L., et al. Progranulin is expressed within motor neurons and promotes neuronal cell survival. BMC Neurosci. 2009, 10:130.
-
(2009)
BMC Neurosci.
, vol.10
, pp. 130
-
-
Ryan, C.L.1
-
84
-
-
42049087853
-
Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
-
jcb.200712039 [pii]
-
Van Damme P., et al. Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival. J. Cell Biol. 2008, 181:37-41. jcb.200712039 [pii]. 10.1083/jcb.200712039.
-
(2008)
J. Cell Biol.
, vol.181
, pp. 37-41
-
-
Van Damme, P.1
-
85
-
-
79953221473
-
Progranulin promotes neurite outgrowth and neuronal differentiation by regulating GSK-3beta
-
Gao X., et al. Progranulin promotes neurite outgrowth and neuronal differentiation by regulating GSK-3beta. Protein Cell 2010, 1:552-562.
-
(2010)
Protein Cell
, vol.1
, pp. 552-562
-
-
Gao, X.1
-
86
-
-
79961232361
-
Progranulin deficiency decreases gross neural connectivity but enhances transmission at individual synapses
-
31/31/11126 [pii]
-
Tapia L., et al. Progranulin deficiency decreases gross neural connectivity but enhances transmission at individual synapses. J. Neurosci. 2011, 31:11126-11132. 31/31/11126 [pii]. 10.1523/JNEUROSCI.6244-10.2011.
-
(2011)
J. Neurosci.
, vol.31
, pp. 11126-11132
-
-
Tapia, L.1
-
87
-
-
84863602114
-
Progranulin regulates neuronal outgrowth independent of sortilin
-
Gass J., et al. Progranulin regulates neuronal outgrowth independent of sortilin. Mol. Neurodegener. 2012, 7:33.
-
(2012)
Mol. Neurodegener.
, vol.7
, pp. 33
-
-
Gass, J.1
-
88
-
-
84855791444
-
Synaptic dysfunction in progranulin-deficient mice
-
Petkau T.L., et al. Synaptic dysfunction in progranulin-deficient mice. Neurobiol. Dis. 2012, 45:711-722.
-
(2012)
Neurobiol. Dis.
, vol.45
, pp. 711-722
-
-
Petkau, T.L.1
-
89
-
-
33749632259
-
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
-
Neumann M., et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006, 314:130-133.
-
(2006)
Science
, vol.314
, pp. 130-133
-
-
Neumann, M.1
-
90
-
-
79251648286
-
Progranulin deficiency leads to enhanced cell vulnerability and TDP-43 translocation in primary neuronal cultures
-
Guo A., et al. Progranulin deficiency leads to enhanced cell vulnerability and TDP-43 translocation in primary neuronal cultures. Brain Res. 2010, 1366:1-8.
-
(2010)
Brain Res.
, vol.1366
, pp. 1-8
-
-
Guo, A.1
-
91
-
-
78651299905
-
Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures
-
Kleinberger G., et al. Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures. J. Neurochem. 2010, 115:735-747.
-
(2010)
J. Neurochem.
, vol.115
, pp. 735-747
-
-
Kleinberger, G.1
-
92
-
-
34848921202
-
Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43
-
Zhang Y.J., et al. Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43. J. Neurosci. 2007, 27:10530-10534.
-
(2007)
J. Neurosci.
, vol.27
, pp. 10530-10534
-
-
Zhang, Y.J.1
-
93
-
-
67650432367
-
Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin
-
Dormann D., et al. Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin. J. Neurochem. 2009, 110:1082-1094.
-
(2009)
J. Neurochem.
, vol.110
, pp. 1082-1094
-
-
Dormann, D.1
-
94
-
-
38349173569
-
Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion
-
Shankaran S.S., et al. Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. J. Biol. Chem. 2008, 283:1744-1753.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 1744-1753
-
-
Shankaran, S.S.1
-
95
-
-
78149296002
-
Behavioral deficits and progressive neuropathology in progranulin-deficient mice: a mouse model of frontotemporal dementia
-
Yin F., et al. Behavioral deficits and progressive neuropathology in progranulin-deficient mice: a mouse model of frontotemporal dementia. FASEB J. 2010, 24:4639-4647.
-
(2010)
FASEB J.
, vol.24
, pp. 4639-4647
-
-
Yin, F.1
-
96
-
-
84864744790
-
Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice
-
Wils H., et al. Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice. J. Pathol. 2012, 228:67-76.
-
(2012)
J. Pathol.
, vol.228
, pp. 67-76
-
-
Wils, H.1
-
97
-
-
84860863883
-
TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells
-
Colombrita C., et al. TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells. J. Biol. Chem. 2012, 287:15635-15647.
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 15635-15647
-
-
Colombrita, C.1
-
98
-
-
78449286213
-
Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin
-
Hu F., et al. Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin. Neuron 2010, 68:654-667.
-
(2010)
Neuron
, vol.68
, pp. 654-667
-
-
Hu, F.1
-
99
-
-
79958831842
-
C-terminus of progranulin interacts with the beta-propeller region of sortilin to regulate progranulin trafficking
-
Zheng Y., et al. C-terminus of progranulin interacts with the beta-propeller region of sortilin to regulate progranulin trafficking. PLoS ONE 2011, 6:e21023. 10.1371/journal.pone.0021023.
-
(2011)
PLoS ONE
, vol.6
-
-
Zheng, Y.1
-
100
-
-
84881553329
-
The neurotrophic properties of progranulin depend on the granulin E domain but do not require sortilin binding
-
De Muynck L., et al. The neurotrophic properties of progranulin depend on the granulin E domain but do not require sortilin binding. Neurobiol. Aging 2013, 34:2541-2547.
-
(2013)
Neurobiol. Aging
, vol.34
, pp. 2541-2547
-
-
De Muynck, L.1
-
101
-
-
84890237444
-
Activity-dependent secretion of progranulin from synapses
-
Petoukhov E., et al. Activity-dependent secretion of progranulin from synapses. J. Cell Sci. 2013, 126:5412-5421.
-
(2013)
J. Cell Sci.
, vol.126
, pp. 5412-5421
-
-
Petoukhov, E.1
-
102
-
-
80054962182
-
Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations
-
Kocerha J., et al. Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations. BMC Genomics 2011, 12:527.
-
(2011)
BMC Genomics
, vol.12
, pp. 527
-
-
Kocerha, J.1
-
103
-
-
84886679297
-
Umbilical cord blood mesenchymal stem cells protect amyloid-beta42 neurotoxicity via paracrine
-
Kim J.Y., et al. Umbilical cord blood mesenchymal stem cells protect amyloid-beta42 neurotoxicity via paracrine. World J. Stem Cells 2012, 4:110-116. 10.4252/wjsc.v4.i11.110.
-
(2012)
World J. Stem Cells
, vol.4
, pp. 110-116
-
-
Kim, J.Y.1
-
104
-
-
84870401656
-
Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects
-
Almeida S., et al. Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects. Cell Rep. 2012, 2:789-798.
-
(2012)
Cell Rep.
, vol.2
, pp. 789-798
-
-
Almeida, S.1
-
105
-
-
84856014831
-
Neuroprotective effects of progranulin in ischemic mice
-
Tao J., et al. Neuroprotective effects of progranulin in ischemic mice. Brain Res. 2012, 1436:130-136.
-
(2012)
Brain Res.
, vol.1436
, pp. 130-136
-
-
Tao, J.1
-
106
-
-
84868623124
-
Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury
-
Martens L.H., et al. Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury. J. Clin. Invest. 2012, 122:3955-3959.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 3955-3959
-
-
Martens, L.H.1
-
107
-
-
84881555971
-
Sensitivity to neurotoxic stress is not increased in progranulin-deficient mice
-
Petkau T.L., et al. Sensitivity to neurotoxic stress is not increased in progranulin-deficient mice. Neurobiol. Aging 2013, 34:2548-2550.
-
(2013)
Neurobiol. Aging
, vol.34
, pp. 2548-2550
-
-
Petkau, T.L.1
-
108
-
-
76149118401
-
Exaggerated inflammation, impaired host defense, and neuropathology in progranulin-deficient mice
-
Yin F., et al. Exaggerated inflammation, impaired host defense, and neuropathology in progranulin-deficient mice. J. Exp. Med. 2010, 207:117-128.
-
(2010)
J. Exp. Med.
, vol.207
, pp. 117-128
-
-
Yin, F.1
-
109
-
-
79251482777
-
Progranulin is a chemoattractant for microglia and stimulates their endocytic activity
-
Pickford F., et al. Progranulin is a chemoattractant for microglia and stimulates their endocytic activity. Am. J. Pathol. 2011, 178:284-295.
-
(2011)
Am. J. Pathol.
, vol.178
, pp. 284-295
-
-
Pickford, F.1
-
110
-
-
84883207887
-
Progranulin promotes activation of microglia/macrophage after pilocarpine-induced status epilepticus
-
Zhu S., et al. Progranulin promotes activation of microglia/macrophage after pilocarpine-induced status epilepticus. Brain Res. 2013, 1530:54-65.
-
(2013)
Brain Res.
, vol.1530
, pp. 54-65
-
-
Zhu, S.1
-
111
-
-
79952712455
-
A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells
-
Kao A.W., et al. A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells. Proc. Natl. Acad. Sci. U.S.A. 2011, 108:4441-4446.
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 4441-4446
-
-
Kao, A.W.1
-
112
-
-
84877099960
-
Dissociation of frontotemporal dementia-related deficits and neuroinflammation in progranulin haploinsufficient mice
-
Filiano A.J., et al. Dissociation of frontotemporal dementia-related deficits and neuroinflammation in progranulin haploinsufficient mice. J. Neurosci. 2013, 33:5352-5361.
-
(2013)
J. Neurosci.
, vol.33
, pp. 5352-5361
-
-
Filiano, A.J.1
-
113
-
-
81955160693
-
Core features of frontotemporal dementia recapitulated in progranulin knockout mice
-
Ghoshal N., et al. Core features of frontotemporal dementia recapitulated in progranulin knockout mice. Neurobiol. Dis. 2012, 45:395-408.
-
(2012)
Neurobiol. Dis.
, vol.45
, pp. 395-408
-
-
Ghoshal, N.1
-
114
-
-
35448929818
-
Alteration of behavioural phenotype in mice by targeted disruption of the progranulin gene
-
Kayasuga Y., et al. Alteration of behavioural phenotype in mice by targeted disruption of the progranulin gene. Behav. Brain Res. 2007, 185:110-118.
-
(2007)
Behav. Brain Res.
, vol.185
, pp. 110-118
-
-
Kayasuga, Y.1
-
115
-
-
40849132907
-
Behavioral phenotyping strategies for mutant mice
-
Crawley J.N. Behavioral phenotyping strategies for mutant mice. Neuron 2008, 57:809-818.
-
(2008)
Neuron
, vol.57
, pp. 809-818
-
-
Crawley, J.N.1
-
116
-
-
84860441181
-
Mouse models of neuronal ceroid lipofuscinoses: useful pre-clinical tools to delineate disease pathophysiology and validate therapeutics
-
Shacka J.J. Mouse models of neuronal ceroid lipofuscinoses: useful pre-clinical tools to delineate disease pathophysiology and validate therapeutics. Brain Res. Bull. 2012, 88:43-57.
-
(2012)
Brain Res. Bull.
, vol.88
, pp. 43-57
-
-
Shacka, J.J.1
-
117
-
-
84881541393
-
Cell biology and function of neuronal ceroid lipofuscinosis-related proteins
-
Kollmann K., et al. Cell biology and function of neuronal ceroid lipofuscinosis-related proteins. Biochim. Biophys. Acta 2013, 1832:1866-1881.
-
(2013)
Biochim. Biophys. Acta
, vol.1832
, pp. 1866-1881
-
-
Kollmann, K.1
-
118
-
-
80455178749
-
Transcriptional gene network inference from a massive dataset elucidates transcriptome organization and gene function
-
Belcastro V., et al. Transcriptional gene network inference from a massive dataset elucidates transcriptome organization and gene function. Nucleic Acids Res. 2011, 39:8677-8688.
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. 8677-8688
-
-
Belcastro, V.1
-
119
-
-
41649092759
-
Structure dissection of human progranulin identifies well-folded granulin/epithelin modules with unique functional activities
-
Tolkatchev D., et al. Structure dissection of human progranulin identifies well-folded granulin/epithelin modules with unique functional activities. Protein Sci. 2008, 17:711-724.
-
(2008)
Protein Sci.
, vol.17
, pp. 711-724
-
-
Tolkatchev, D.1
|