-
1
-
-
84860580995
-
Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion
-
Allen N.M., O'hici B., Anderson G., Nestor T., Ann Lynch S., King M. Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion. Clin. Genet. 2012, 81:602-604.
-
(2012)
Clin. Genet.
, vol.81
, pp. 602-604
-
-
Allen, N.M.1
O'hici, B.2
Anderson, G.3
Nestor, T.4
Ann Lynch, S.5
King, M.6
-
2
-
-
34447100391
-
Decreased T2 signal in the thalami may be a sign of lysosomal storage disease
-
Autti T., Joensuu R., Aberg L. Decreased T2 signal in the thalami may be a sign of lysosomal storage disease. Neuroradiology 2007, 49:571-578.
-
(2007)
Neuroradiology
, vol.49
, pp. 571-578
-
-
Autti, T.1
Joensuu, R.2
Aberg, L.3
-
3
-
-
55049084760
-
The mystery and magic of glia: a perspective on their roles in health and disease
-
Barres B.A. The mystery and magic of glia: a perspective on their roles in health and disease. Neuron 2008, 60:430-440.
-
(2008)
Neuron
, vol.60
, pp. 430-440
-
-
Barres, B.A.1
-
4
-
-
0027465678
-
Synaptosomal glutamate uptake declines progressively in the spinal cord of a mutant mouse with motor neuron disease
-
Battaglioli G., Martin D.L., Plummer J., Messer A. Synaptosomal glutamate uptake declines progressively in the spinal cord of a mutant mouse with motor neuron disease. J. Neurochem. 1993, 60:1567-1569.
-
(1993)
J. Neurochem.
, vol.60
, pp. 1567-1569
-
-
Battaglioli, G.1
Martin, D.L.2
Plummer, J.3
Messer, A.4
-
5
-
-
0036929577
-
Mitochondrial oxidative metabolism in motor neuron degeneration (mnd) mouse central nervous system
-
Bertamini M., Marzani B., Guarneri R., Guarneri P., Bigini P., Mennini T., et al. Mitochondrial oxidative metabolism in motor neuron degeneration (mnd) mouse central nervous system. Eur. J. Neurosci. 2002, 16:2291-2296.
-
(2002)
Eur. J. Neurosci.
, vol.16
, pp. 2291-2296
-
-
Bertamini, M.1
Marzani, B.2
Guarneri, R.3
Guarneri, P.4
Bigini, P.5
Mennini, T.6
-
6
-
-
35748939409
-
Neuronal 'on' and 'off' signals control microglia
-
Biber K., Neumann H., Inoue K., Boddeke H.W. Neuronal 'on' and 'off' signals control microglia. Trends Neurosci. 2007, 30:596-602.
-
(2007)
Trends Neurosci.
, vol.30
, pp. 596-602
-
-
Biber, K.1
Neumann, H.2
Inoue, K.3
Boddeke, H.W.4
-
7
-
-
0037165915
-
The development of behavioral abnormalities in the motor neuron degeneration (mnd) mouse
-
Bolivar V.J., Scott Ganus J., Messer A. The development of behavioral abnormalities in the motor neuron degeneration (mnd) mouse. Brain Res. 2002, 937:74-82.
-
(2002)
Brain Res.
, vol.937
, pp. 74-82
-
-
Bolivar, V.J.1
Scott Ganus, J.2
Messer, A.3
-
8
-
-
0033044037
-
Onset and progression of motor deficits in motor neuron degeneration (mnd) mice are unaltered by the glycine/NMDA receptor antagonist L-701,324 or the MAO-B inhibitor R(-)-deprenyl
-
Boyce S., Webb J.K., Carlson E., Rupniak N.M., Hill R.G., Martin J.E. Onset and progression of motor deficits in motor neuron degeneration (mnd) mice are unaltered by the glycine/NMDA receptor antagonist L-701,324 or the MAO-B inhibitor R(-)-deprenyl. Exp. Neurol. 1999, 155:49-58.
-
(1999)
Exp. Neurol.
, vol.155
, pp. 49-58
-
-
Boyce, S.1
Webb, J.K.2
Carlson, E.3
Rupniak, N.M.4
Hill, R.G.5
Martin, J.E.6
-
9
-
-
84861723960
-
Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis
-
(Electronic publication ahead of print)
-
Bras J., Verloes A., Schneider S.A., Mole S.E., Guerreiro R.J. Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis. Hum. Mol. Genet. 2012, (Electronic publication ahead of print). 10.1093/hmg/dds089.
-
(2012)
Hum. Mol. Genet.
-
-
Bras, J.1
Verloes, A.2
Schneider, S.A.3
Mole, S.E.4
Guerreiro, R.J.5
-
10
-
-
0027453099
-
Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)
-
Bronson R.T., Lake B.D., Cook S., Taylor S., Davisson M.T. Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease). Ann. Neurol. 1993, 33:381-385.
-
(1993)
Ann. Neurol.
, vol.33
, pp. 381-385
-
-
Bronson, R.T.1
Lake, B.D.2
Cook, S.3
Taylor, S.4
Davisson, M.T.5
-
11
-
-
33646396485
-
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean
-
Cannelli N., Cassandrini D., Bertini E., Striano P., Fusco L., Gaggero R., et al. Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean. Neurogenetics 2006, 7:111-117.
-
(2006)
Neurogenetics
, vol.7
, pp. 111-117
-
-
Cannelli, N.1
Cassandrini, D.2
Bertini, E.3
Striano, P.4
Fusco, L.5
Gaggero, R.6
-
12
-
-
63849213783
-
Inflammation triggers synaptic alteration and degeneration in experimental autoimmune encephalomyelitis
-
Centonze D., Muzio L., Rossi S., Cavasinni F., De Chiara V., Bergami A., et al. Inflammation triggers synaptic alteration and degeneration in experimental autoimmune encephalomyelitis. J. Neurosci. 2009, 29:3442-3452.
-
(2009)
J. Neurosci.
, vol.29
, pp. 3442-3452
-
-
Centonze, D.1
Muzio, L.2
Rossi, S.3
Cavasinni, F.4
De Chiara, V.5
Bergami, A.6
-
13
-
-
0028216385
-
Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis
-
Chang B., Bronson R.T., Hawes N.L., Roderick T.H., Peng C., Hageman G.S., et al. Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis. Invest. Ophthalmol. Vis. Sci. 1994, 35:1071-1076.
-
(1994)
Invest. Ophthalmol. Vis. Sci.
, vol.35
, pp. 1071-1076
-
-
Chang, B.1
Bronson, R.T.2
Hawes, N.L.3
Roderick, T.H.4
Peng, C.5
Hageman, G.S.6
-
14
-
-
41149092265
-
Intraventricular enzyme replacement improves disease phenotypes in a mouse model of late infantile neuronal ceroid lipofuscinosis
-
Chang M., Cooper J.D., Sleat D.E., Cheng S.H., Dodge J.C., Passini M.A., et al. Intraventricular enzyme replacement improves disease phenotypes in a mouse model of late infantile neuronal ceroid lipofuscinosis. Mol. Ther. 2008, 16:649-656.
-
(2008)
Mol. Ther.
, vol.16
, pp. 649-656
-
-
Chang, M.1
Cooper, J.D.2
Sleat, D.E.3
Cheng, S.H.4
Dodge, J.C.5
Passini, M.A.6
-
15
-
-
78649747041
-
The neuronal ceroid lipofuscinoses: the same, but different?
-
Cooper J.D. The neuronal ceroid lipofuscinoses: the same, but different?. Biochem. Soc. Trans. 2010, 38:1448-1452.
-
(2010)
Biochem. Soc. Trans.
, vol.38
, pp. 1448-1452
-
-
Cooper, J.D.1
-
16
-
-
33750976371
-
Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis
-
Cooper J.D., Russell C., Mitchison H.M. Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis. Biochim. Biophys. Acta 2006, 1762:873-889.
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 873-889
-
-
Cooper, J.D.1
Russell, C.2
Mitchison, H.M.3
-
17
-
-
0033119124
-
Apparent loss and hypertrophy of interneurons in a mouse model of neuronal ceroid lipofuscinosis: evidence for partial response to insulin-like growth factor-1 treatment
-
Cooper J.D., Messer A., Feng A.K., Chua-Couzens J., Mobley W.C. Apparent loss and hypertrophy of interneurons in a mouse model of neuronal ceroid lipofuscinosis: evidence for partial response to insulin-like growth factor-1 treatment. J. Neurosci. 1999, 19:2556-2567.
-
(1999)
J. Neurosci.
, vol.19
, pp. 2556-2567
-
-
Cooper, J.D.1
Messer, A.2
Feng, A.K.3
Chua-Couzens, J.4
Mobley, W.C.5
-
18
-
-
78650817466
-
Different early ER-stress responses in the CLN8(mnd) mouse model of neuronal ceroid lipofuscinosis
-
Galizzi G., Russo D., Deidda I., Cascio C., Passantino R., Guarneri R., et al. Different early ER-stress responses in the CLN8(mnd) mouse model of neuronal ceroid lipofuscinosis. Neurosci. Lett. 2011, 488:258-262.
-
(2011)
Neurosci. Lett.
, vol.488
, pp. 258-262
-
-
Galizzi, G.1
Russo, D.2
Deidda, I.3
Cascio, C.4
Passantino, R.5
Guarneri, R.6
-
19
-
-
0036155235
-
Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse
-
Gao H., Boustany R.M., Espinola J.A., Cotman S.L., Srinidhi L., Antonellis K.A., et al. Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse. Am. J. Hum. Genet. 2002, 70:324-335.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 324-335
-
-
Gao, H.1
Boustany, R.M.2
Espinola, J.A.3
Cotman, S.L.4
Srinidhi, L.5
Antonellis, K.A.6
-
20
-
-
0031841018
-
Tumor necrosis factor is increased in the spinal cord of an animal model of motor neuron degeneration
-
Ghezzi P., Bernardini R., Giuffrida R., Bellomo M., Manzoni C., Comoletti D., et al. Tumor necrosis factor is increased in the spinal cord of an animal model of motor neuron degeneration. Eur. Cytokine Netw. 1998, 9:139-144.
-
(1998)
Eur. Cytokine Netw.
, vol.9
, pp. 139-144
-
-
Ghezzi, P.1
Bernardini, R.2
Giuffrida, R.3
Bellomo, M.4
Manzoni, C.5
Comoletti, D.6
-
21
-
-
0032846760
-
Long-term neuroprotective effects of glycosaminoglycans-IGF-I cotreatment in the motor neuron degeneration (mnd) mutant mouse
-
Gorio A., Germani E., Lesma E., Rossoni G., Muller E.E., Di Giulio A.M. Long-term neuroprotective effects of glycosaminoglycans-IGF-I cotreatment in the motor neuron degeneration (mnd) mutant mouse. Eur. J. Neurosci. 1999, 11:3395-3404.
-
(1999)
Eur. J. Neurosci.
, vol.11
, pp. 3395-3404
-
-
Gorio, A.1
Germani, E.2
Lesma, E.3
Rossoni, G.4
Muller, E.E.5
Di Giulio, A.M.6
-
22
-
-
2942699883
-
Retinal oxidation, apoptosis and age- and sex-differences in the mnd mutant mouse, a model of neuronal ceroid lipofuscinosis
-
Guarneri R., Russo D., Cascio C., D'Agostino S., Galizzi G., Bigini P., et al. Retinal oxidation, apoptosis and age- and sex-differences in the mnd mutant mouse, a model of neuronal ceroid lipofuscinosis. Brain Res. 2004, 1014:209-220.
-
(2004)
Brain Res.
, vol.1014
, pp. 209-220
-
-
Guarneri, R.1
Russo, D.2
Cascio, C.3
D'Agostino, S.4
Galizzi, G.5
Bigini, P.6
-
23
-
-
84985280160
-
The efficiency of systematic sampling in stereology and its prediction
-
Gundersen H.J., Jensen E.B. The efficiency of systematic sampling in stereology and its prediction. J. Microsc. 1987, 147:229-263.
-
(1987)
J. Microsc.
, vol.147
, pp. 229-263
-
-
Gundersen, H.J.1
Jensen, E.B.2
-
24
-
-
0037226939
-
The neuronal ceroid-lipofuscinoses
-
Haltia M. The neuronal ceroid-lipofuscinoses. J. Neuropathol. Exp. Neurol. 2003, 62:1-13.
-
(2003)
J. Neuropathol. Exp. Neurol.
, vol.62
, pp. 1-13
-
-
Haltia, M.1
-
25
-
-
0015815856
-
Infantile type of so-called neuronal ceroid-lipofuscinosis. histological and electron microscopic studies
-
Haltia M., Rapola J., Santavuori P. Infantile type of so-called neuronal ceroid-lipofuscinosis. histological and electron microscopic studies. Acta Neuropathol. 1973, 26:157-170.
-
(1973)
Acta Neuropathol.
, vol.26
, pp. 157-170
-
-
Haltia, M.1
Rapola, J.2
Santavuori, P.3
-
26
-
-
0035287432
-
GLIA: listening and talking to the synapse
-
Haydon P.G. GLIA: listening and talking to the synapse. Nat. Rev. Neurosci. 2001, 2:185-193.
-
(2001)
Nat. Rev. Neurosci.
, vol.2
, pp. 185-193
-
-
Haydon, P.G.1
-
27
-
-
0034112242
-
Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis
-
Herva R., Tyynela J., Hirvasniemi A., Syrjakallio-Ylitalo M., Haltia M. Northern epilepsy: a novel form of neuronal ceroid-lipofuscinosis. Brain Pathol. 2000, 10:215-222.
-
(2000)
Brain Pathol.
, vol.10
, pp. 215-222
-
-
Herva, R.1
Tyynela, J.2
Hirvasniemi, A.3
Syrjakallio-Ylitalo, M.4
Haltia, M.5
-
28
-
-
0029133189
-
Northern epilepsy syndrome: clinical course and the effect of medication on seizures
-
Hirvasniemi A., Herrala P., Leisti J. Northern epilepsy syndrome: clinical course and the effect of medication on seizures. Epilepsia 1995, 36:792-797.
-
(1995)
Epilepsia
, vol.36
, pp. 792-797
-
-
Hirvasniemi, A.1
Herrala, P.2
Leisti, J.3
-
29
-
-
0028345785
-
Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration
-
Hirvasniemi A., Lang H., Lehesjoki A.E., Leisti J. Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration. J. Med. Genet. 1994, 31:177-182.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 177-182
-
-
Hirvasniemi, A.1
Lang, H.2
Lehesjoki, A.E.3
Leisti, J.4
-
30
-
-
0029147298
-
The International Batten Disease Consortium Isolation of a novel gene underlying Batten disease, CLN3
-
The International Batten Disease Consortium Isolation of a novel gene underlying Batten disease, CLN3. Cell 1995, 82:949-957.
-
(1995)
Cell
, vol.82
, pp. 949-957
-
-
-
31
-
-
33745018230
-
Activation of non-neuronal cells within the prenatal developing brain of sheep with neuronal ceroid lipofuscinosis
-
Kay G.W., Palmer D.N., Rezaie P., Cooper J.D. Activation of non-neuronal cells within the prenatal developing brain of sheep with neuronal ceroid lipofuscinosis. Brain Pathol. 2006, 16:110-116.
-
(2006)
Brain Pathol.
, vol.16
, pp. 110-116
-
-
Kay, G.W.1
Palmer, D.N.2
Rezaie, P.3
Cooper, J.D.4
-
32
-
-
80052827401
-
Inflammation in the early stages of neurodegenerative pathology
-
Khandelwal P.J., Herman A.M., Moussa C.E. Inflammation in the early stages of neurodegenerative pathology. J. Neuroimmunol. 2011, 238:1-11.
-
(2011)
J. Neuroimmunol.
, vol.238
, pp. 1-11
-
-
Khandelwal, P.J.1
Herman, A.M.2
Moussa, C.E.3
-
33
-
-
70349997680
-
Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease
-
Kielar C., Wishart T.M., Palmer A., Dihanich S., Wong A.M., Macauley S.L., et al. Molecular correlates of axonal and synaptic pathology in mouse models of Batten disease. Hum. Mol. Genet. 2009, 18:4066-4080.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 4066-4080
-
-
Kielar, C.1
Wishart, T.M.2
Palmer, A.3
Dihanich, S.4
Wong, A.M.5
Macauley, S.L.6
-
34
-
-
33751349970
-
Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis
-
Kielar C., Maddox L., Bible E., Pontikis C.C., Macauley S.L., Griffey M.A., et al. Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis. Neurobiol. Dis. 2007, 25:150-162.
-
(2007)
Neurobiol. Dis.
, vol.25
, pp. 150-162
-
-
Kielar, C.1
Maddox, L.2
Bible, E.3
Pontikis, C.C.4
Macauley, S.L.5
Griffey, M.A.6
-
35
-
-
51349089035
-
Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice
-
Kim S.J., Zhang Z., Sarkar C., Tsai P.C., Lee Y.C., Dye L., et al. Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice. J. Clin. Invest. 2008, 118:3075-3086.
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 3075-3086
-
-
Kim, S.J.1
Zhang, Z.2
Sarkar, C.3
Tsai, P.C.4
Lee, Y.C.5
Dye, L.6
-
36
-
-
79251479743
-
Myoclonic disorders: a practical approach for diagnosis and treatment
-
Kojovic M., Cordivari C., Bhatia K. Myoclonic disorders: a practical approach for diagnosis and treatment. Ther. Adv. Neurol. Disord. 2011, 4:47-62.
-
(2011)
Ther. Adv. Neurol. Disord.
, vol.4
, pp. 47-62
-
-
Kojovic, M.1
Cordivari, C.2
Bhatia, K.3
-
37
-
-
82855165086
-
Deficient mitochondrial Ca(2+) buffering in the Cln8(mnd) mouse model of neuronal ceroid lipofuscinosis
-
Kolikova J., Afzalov R., Surin A., Lehesjoki A.E., Khiroug L. Deficient mitochondrial Ca(2+) buffering in the Cln8(mnd) mouse model of neuronal ceroid lipofuscinosis. Cell Calcium 2011, 50:491-501.
-
(2011)
Cell Calcium
, vol.50
, pp. 491-501
-
-
Kolikova, J.1
Afzalov, R.2
Surin, A.3
Lehesjoki, A.E.4
Khiroug, L.5
-
38
-
-
64849091209
-
Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis
-
Kousi M., Siintola E., Dvorakova L., Vlaskova H., Turnbull J., Topcu M., et al. Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis. Brain 2009, 132:810-819.
-
(2009)
Brain
, vol.132
, pp. 810-819
-
-
Kousi, M.1
Siintola, E.2
Dvorakova, L.3
Vlaskova, H.4
Turnbull, J.5
Topcu, M.6
-
39
-
-
84863469926
-
Galactolipid deficiency in the early pathogenesis of neuronal ceroid lipofuscinosis model Cln8(mnd): implications to delayed myelination and oligodendrocyte maturation
-
( 2011 Nov 2, Electronic publication ahead of print)
-
Kuronen M., Hermansson M., Manninen O., Zech I., Talvitie M., Laitinen T., et al. Galactolipid deficiency in the early pathogenesis of neuronal ceroid lipofuscinosis model Cln8(mnd): implications to delayed myelination and oligodendrocyte maturation. Neuropathol. Appl. Neurobiol. 2012, ( 2011 Nov 2, Electronic publication ahead of print). 10.1111/j.1365-2990.2011.01233.x.
-
(2012)
Neuropathol. Appl. Neurobiol.
-
-
Kuronen, M.1
Hermansson, M.2
Manninen, O.3
Zech, I.4
Talvitie, M.5
Laitinen, T.6
-
40
-
-
0031051650
-
Neurophysiological findings in the northern epilepsy syndrome
-
Lang A.H., Hirvasniemi A., Siivola J. Neurophysiological findings in the northern epilepsy syndrome. Acta Neurol. Scand. 1997, 95:1-8.
-
(1997)
Acta Neurol. Scand.
, vol.95
, pp. 1-8
-
-
Lang, A.H.1
Hirvasniemi, A.2
Siivola, J.3
-
41
-
-
0034916520
-
Northern epilepsy syndrome (NES, CLN8)-MRI and electrophysiological studies
-
Lauronen L., Santavuori P., Hirvasniemi A., Kirveskari E., Huttunen J., Autti T. Northern epilepsy syndrome (NES, CLN8)-MRI and electrophysiological studies. Eur. J. Paediatr. Neurol. 2001, 5(Suppl. A):167-173.
-
(2001)
Eur. J. Paediatr. Neurol.
, vol.5
, Issue.SUPPL. A
, pp. 167-173
-
-
Lauronen, L.1
Santavuori, P.2
Hirvasniemi, A.3
Kirveskari, E.4
Huttunen, J.5
Autti, T.6
-
42
-
-
0030968569
-
Somatosensory evoked magnetic fields from primary sensorimotor cortex in juvenile neuronal ceroid lipofuscinosis
-
Lauronen L., Heikkila E., Autti T., Sainio K., Huttunen J., Aronen H.J., et al. Somatosensory evoked magnetic fields from primary sensorimotor cortex in juvenile neuronal ceroid lipofuscinosis. J. Child. Neurol. 1997, 12:355-360.
-
(1997)
J. Child. Neurol.
, vol.12
, pp. 355-360
-
-
Lauronen, L.1
Heikkila, E.2
Autti, T.3
Sainio, K.4
Huttunen, J.5
Aronen, H.J.6
-
43
-
-
80051782344
-
Cross talk between activation of microglia and astrocytes in pathological conditions in the central nervous system
-
Liu W., Tang Y., Feng J. Cross talk between activation of microglia and astrocytes in pathological conditions in the central nervous system. Life Sci. 2011, 89:141-146.
-
(2011)
Life Sci.
, vol.89
, pp. 141-146
-
-
Liu, W.1
Tang, Y.2
Feng, J.3
-
44
-
-
26444449018
-
The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy
-
Lonka L., Aalto A., Kopra O., Kuronen M., Kokaia Z., Saarma M., et al. The neuronal ceroid lipofuscinosis Cln8 gene expression is developmentally regulated in mouse brain and up-regulated in the hippocampal kindling model of epilepsy. BMC Neurosci. 2005, 6:27.
-
(2005)
BMC Neurosci.
, vol.6
, pp. 27
-
-
Lonka, L.1
Aalto, A.2
Kopra, O.3
Kuronen, M.4
Kokaia, Z.5
Saarma, M.6
-
45
-
-
2642510804
-
Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells
-
Lonka L., Salonen T., Siintola E., Kopra O., Lehesjoki A.E., Jalanko A. Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells. J. Neurosci. Res. 2004, 76:862-871.
-
(2004)
J. Neurosci. Res.
, vol.76
, pp. 862-871
-
-
Lonka, L.1
Salonen, T.2
Siintola, E.3
Kopra, O.4
Lehesjoki, A.E.5
Jalanko, A.6
-
46
-
-
18844471093
-
The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum
-
Lonka L., Kyttala A., Ranta S., Jalanko A., Lehesjoki A.E. The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum. Hum. Mol. Genet. 2000, 9:1691-1697.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1691-1697
-
-
Lonka, L.1
Kyttala, A.2
Ranta, S.3
Jalanko, A.4
Lehesjoki, A.E.5
-
47
-
-
64549084081
-
Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse
-
Macauley S.L., Wozniak D.F., Kielar C., Tan Y., Cooper J.D., Sands M.S. Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouse. Exp. Neurol. 2009, 217:124-135.
-
(2009)
Exp. Neurol.
, vol.217
, pp. 124-135
-
-
Macauley, S.L.1
Wozniak, D.F.2
Kielar, C.3
Tan, Y.4
Cooper, J.D.5
Sands, M.S.6
-
48
-
-
78649995400
-
Neuronal hyperexcitability and seizures are associated with changes in glial-neuronal interactions in the hippocampus of a mouse model of epilepsy with mental retardation
-
Melo T., Bigini P., Sonnewald U., Balosso S., Cagnotto A., Barbera S., et al. Neuronal hyperexcitability and seizures are associated with changes in glial-neuronal interactions in the hippocampus of a mouse model of epilepsy with mental retardation. J. Neurochem. 2010, 115:1445-1454.
-
(2010)
J. Neurochem.
, vol.115
, pp. 1445-1454
-
-
Melo, T.1
Bigini, P.2
Sonnewald, U.3
Balosso, S.4
Cagnotto, A.5
Barbera, S.6
-
49
-
-
0347931850
-
Glial activation and TNFR-I upregulation precedes motor dysfunction in the spinal cord of mnd mice
-
Mennini T., Bigini P., Cagnotto A., Carvelli L., Di Nunno P., Fumagalli E., et al. Glial activation and TNFR-I upregulation precedes motor dysfunction in the spinal cord of mnd mice. Cytokine 2004, 25:127-135.
-
(2004)
Cytokine
, vol.25
, pp. 127-135
-
-
Mennini, T.1
Bigini, P.2
Cagnotto, A.3
Carvelli, L.4
Di Nunno, P.5
Fumagalli, E.6
-
50
-
-
0037110681
-
Expression of glutamate receptor subtypes in the spinal cord of control and mnd mice, a model of motor neuron disorder
-
Mennini T., Bigini P., Ravizza T., Vezzani A., Calvaresi N., Tortarolo M., et al. Expression of glutamate receptor subtypes in the spinal cord of control and mnd mice, a model of motor neuron disorder. J. Neurosci. Res. 2002, 70:553-560.
-
(2002)
J. Neurosci. Res.
, vol.70
, pp. 553-560
-
-
Mennini, T.1
Bigini, P.2
Ravizza, T.3
Vezzani, A.4
Calvaresi, N.5
Tortarolo, M.6
-
51
-
-
0032522699
-
Spinal cord GLT-1 glutamate transporter and blood glutamic acid alterations in motor neuron degeneration (mnd) mice
-
Mennini T., Bastone A., Crespi D., Comoletti D., Manzoni C. Spinal cord GLT-1 glutamate transporter and blood glutamic acid alterations in motor neuron degeneration (mnd) mice. J. Neurol. Sci. 1998, 157:31-36.
-
(1998)
J. Neurol. Sci.
, vol.157
, pp. 31-36
-
-
Mennini, T.1
Bastone, A.2
Crespi, D.3
Comoletti, D.4
Manzoni, C.5
-
52
-
-
0027384717
-
Retinal degeneration in motor neuron degeneration (mnd) mutant mice
-
Messer A., Plummer J., Wong V., Lavail M.M. Retinal degeneration in motor neuron degeneration (mnd) mutant mice. Exp. Eye Res. 1993, 57:637-641.
-
(1993)
Exp. Eye Res.
, vol.57
, pp. 637-641
-
-
Messer, A.1
Plummer, J.2
Wong, V.3
Lavail, M.M.4
-
53
-
-
0023212297
-
Histopathology of the late-onset motor neuron degeneration (mnd) mutant in the mouse
-
Messer A., Strominger N.L., Mazurkiewicz J.E. Histopathology of the late-onset motor neuron degeneration (mnd) mutant in the mouse. J. Neurogenet. 1987, 4:201-213.
-
(1987)
J. Neurogenet.
, vol.4
, pp. 201-213
-
-
Messer, A.1
Strominger, N.L.2
Mazurkiewicz, J.E.3
-
54
-
-
0022976796
-
Autosomal dominance in a late-onset motor neuron disease in the mouse
-
Messer A., Flaherty L. Autosomal dominance in a late-onset motor neuron disease in the mouse. J. Neurogenet. 1986, 3:345-355.
-
(1986)
J. Neurogenet.
, vol.3
, pp. 345-355
-
-
Messer, A.1
Flaherty, L.2
-
55
-
-
0031921360
-
Cortical myoclonus: sensorimotor hyperexcitability
-
Mima T., Nagamine T., Nishitani N., Mikuni N., Ikeda A., Fukuyama H., et al. Cortical myoclonus: sensorimotor hyperexcitability. Neurology 1998, 50:933-942.
-
(1998)
Neurology
, vol.50
, pp. 933-942
-
-
Mima, T.1
Nagamine, T.2
Nishitani, N.3
Mikuni, N.4
Ikeda, A.5
Fukuyama, H.6
-
56
-
-
80051672679
-
Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis
-
Noskova L., Stranecky V., Hartmannova H., Pristoupilova A., Baresova V., Ivanek R., et al. Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis. Am. J. Hum. Genet. 2011, 89:241-252.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 241-252
-
-
Noskova, L.1
Stranecky, V.2
Hartmannova, H.3
Pristoupilova, A.4
Baresova, V.5
Ivanek, R.6
-
57
-
-
24044496235
-
Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6)
-
Oswald M.J., Palmer D.N., Kay G.W., Shemilt S.J., Rezaie P., Cooper J.D. Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6). Neurobiol. Dis. 2005, 20:49-63.
-
(2005)
Neurobiol. Dis.
, vol.20
, pp. 49-63
-
-
Oswald, M.J.1
Palmer, D.N.2
Kay, G.W.3
Shemilt, S.J.4
Rezaie, P.5
Cooper, J.D.6
-
58
-
-
0028240480
-
Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis
-
Pardo C.A., Rabin B.A., Palmer D.N., Price D.L. Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis. Am. J. Pathol. 1994, 144:829-835.
-
(1994)
Am. J. Pathol.
, vol.144
, pp. 829-835
-
-
Pardo, C.A.1
Rabin, B.A.2
Palmer, D.N.3
Price, D.L.4
-
59
-
-
37549057968
-
Synaptic changes in the thalamocortical system of cathepsin D-deficient mice: a model of human congenital neuronal ceroid-lipofuscinosis
-
Partanen S., Haapanen A., Kielar C., Pontikis C., Alexander N., Inkinen T., et al. Synaptic changes in the thalamocortical system of cathepsin D-deficient mice: a model of human congenital neuronal ceroid-lipofuscinosis. J. Neuropathol. Exp. Neurol. 2008, 67:16-29.
-
(2008)
J. Neuropathol. Exp. Neurol.
, vol.67
, pp. 16-29
-
-
Partanen, S.1
Haapanen, A.2
Kielar, C.3
Pontikis, C.4
Alexander, N.5
Inkinen, T.6
-
61
-
-
0029557363
-
Accelerated and widespread neuronal loss occurs in motor neuron degeneration (mnd) mice expressing a neurofilament-disrupting transgene
-
Plummer J., Peterson A., Messer A. Accelerated and widespread neuronal loss occurs in motor neuron degeneration (mnd) mice expressing a neurofilament-disrupting transgene. Mol. Cell. Neurosci. 1995, 6:532-543.
-
(1995)
Mol. Cell. Neurosci.
, vol.6
, pp. 532-543
-
-
Plummer, J.1
Peterson, A.2
Messer, A.3
-
62
-
-
27744565604
-
Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten disease
-
Pontikis C.C., Cotman S.L., MacDonald M.E., Cooper J.D. Thalamocortical neuron loss and localized astrocytosis in the Cln3Deltaex7/8 knock-in mouse model of Batten disease. Neurobiol. Dis. 2005, 20:823-836.
-
(2005)
Neurobiol. Dis.
, vol.20
, pp. 823-836
-
-
Pontikis, C.C.1
Cotman, S.L.2
MacDonald, M.E.3
Cooper, J.D.4
-
64
-
-
11144353883
-
Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to northern epilepsy
-
Ranta S., Topcu M., Tegelberg S., Tan H., Ustubutun A., Saatci I., et al. Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to northern epilepsy. Hum. Mutat. 2004, 23:300-305.
-
(2004)
Hum. Mutat.
, vol.23
, pp. 300-305
-
-
Ranta, S.1
Topcu, M.2
Tegelberg, S.3
Tan, H.4
Ustubutun, A.5
Saatci, I.6
-
65
-
-
0032831071
-
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8
-
Ranta S., Zhang Y., Ross B., Lonka L., Takkunen E., Messer A., et al. The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nat. Genet. 1999, 23:233-236.
-
(1999)
Nat. Genet.
, vol.23
, pp. 233-236
-
-
Ranta, S.1
Zhang, Y.2
Ross, B.3
Lonka, L.4
Takkunen, E.5
Messer, A.6
-
66
-
-
73049116738
-
Novel CLN8 mutations confirm the clinical and ethnic diversity of late infantile neuronal ceroid lipofuscinosis
-
Reinhardt K., Grapp M., Schlachter K., Bruck W., Gartner J., Steinfeld R. Novel CLN8 mutations confirm the clinical and ethnic diversity of late infantile neuronal ceroid lipofuscinosis. Clin. Genet. 2010, 77:79-85.
-
(2010)
Clin. Genet.
, vol.77
, pp. 79-85
-
-
Reinhardt, K.1
Grapp, M.2
Schlachter, K.3
Bruck, W.4
Gartner, J.5
Steinfeld, R.6
-
67
-
-
0025736263
-
The spectrum of Jansky-Bielschowsky disease
-
Santavuori P., Rapola J., Nuutila A., Raininko R., Lappi M., Launes J., et al. The spectrum of Jansky-Bielschowsky disease. Neuropediatrics 1991, 22:92-96.
-
(1991)
Neuropediatrics
, vol.22
, pp. 92-96
-
-
Santavuori, P.1
Rapola, J.2
Nuutila, A.3
Raininko, R.4
Lappi, M.5
Launes, J.6
-
68
-
-
0031803649
-
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis
-
Savukoski M., Klockars T., Holmberg V., Santavuori P., Lander E.S., Peltonen L. CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis. Nat. Genet. 1998, 19:286-288.
-
(1998)
Nat. Genet.
, vol.19
, pp. 286-288
-
-
Savukoski, M.1
Klockars, T.2
Holmberg, V.3
Santavuori, P.4
Lander, E.S.5
Peltonen, L.6
-
69
-
-
84858158434
-
Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism
-
Schmiedt M.L., Blom T., Blom T., Kopra O., Wong A., von Schantz-Fant C., et al. Cln5-deficiency in mice leads to microglial activation, defective myelination and changes in lipid metabolism. Neurobiol. Dis. 2012, 46:19-29.
-
(2012)
Neurobiol. Dis.
, vol.46
, pp. 19-29
-
-
Schmiedt, M.L.1
Blom, T.2
Blom, T.3
Kopra, O.4
Wong, A.5
von Schantz-Fant, C.6
-
70
-
-
0028234965
-
Somatosensory evoked potentials with high cortical amplitudes: clinical data in 31 children
-
Schmitt B., Thun-Hohenstein L., Molinari L., Superti-Furga A., Boltshauser E. Somatosensory evoked potentials with high cortical amplitudes: clinical data in 31 children. Neuropediatrics 1994, 25:78-84.
-
(1994)
Neuropediatrics
, vol.25
, pp. 78-84
-
-
Schmitt, B.1
Thun-Hohenstein, L.2
Molinari, L.3
Superti-Furga, A.4
Boltshauser, E.5
-
71
-
-
31444445870
-
Progression of early postnatal retinal pathology in a mouse model of neuronal ceroid lipofuscinosis
-
Seigel G.M., Wagner J., Wronska A., Campbell L., Ju W., Zhong N. Progression of early postnatal retinal pathology in a mouse model of neuronal ceroid lipofuscinosis. Eye 2005, 19:1306-1312.
-
(2005)
Eye
, vol.19
, pp. 1306-1312
-
-
Seigel, G.M.1
Wagner, J.2
Wronska, A.3
Campbell, L.4
Ju, W.5
Zhong, N.6
-
72
-
-
34347253609
-
The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter
-
Siintola E., Topcu M., Aula N., Lohi H., Minassian B.A., Paterson A.D., et al. The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter. Am. J. Hum. Genet. 2007, 81:136-146.
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 136-146
-
-
Siintola, E.1
Topcu, M.2
Aula, N.3
Lohi, H.4
Minassian, B.A.5
Paterson, A.D.6
-
73
-
-
33745079623
-
Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis
-
Siintola E., Partanen S., Stromme P., Haapanen A., Haltia M., Maehlen J., et al. Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis. Brain 2006, 129:1438-1445.
-
(2006)
Brain
, vol.129
, pp. 1438-1445
-
-
Siintola, E.1
Partanen, S.2
Stromme, P.3
Haapanen, A.4
Haltia, M.5
Maehlen, J.6
-
74
-
-
0030866233
-
Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis
-
Sleat D.E., Donnelly R.J., Lackland H., Liu C.G., Sohar I., Pullarkat R.K., et al. Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis. Science 1997, 277:1802-1805.
-
(1997)
Science
, vol.277
, pp. 1802-1805
-
-
Sleat, D.E.1
Donnelly, R.J.2
Lackland, H.3
Liu, C.G.4
Sohar, I.5
Pullarkat, R.K.6
-
75
-
-
0018645886
-
Evoked potentials in neuronal ceroid lipofuscinosis
-
Tackmann W., Kuhlendahl D. Evoked potentials in neuronal ceroid lipofuscinosis. Eur. Neurol. 1979, 18:234-242.
-
(1979)
Eur. Neurol.
, vol.18
, pp. 234-242
-
-
Tackmann, W.1
Kuhlendahl, D.2
-
76
-
-
84655161991
-
-/- mouse model of progressive myoclonus epilepsy, EPM1
-
-/- mouse model of progressive myoclonus epilepsy, EPM1. J. Neuropathol. Exp. Neurol. 2012, 71:40-53.
-
(2012)
J. Neuropathol. Exp. Neurol.
, vol.71
, pp. 40-53
-
-
Tegelberg, S.1
Kopra, O.2
Joensuu, T.3
Cooper, J.D.4
Lehesjoki, A.E.5
-
77
-
-
12144288248
-
Evaluation of 36 patients from Turkey with neuronal ceroid lipofuscinosis: clinical, neurophysiological, neuroradiological and histopathologic studies
-
Topcu M., Tan H., Yalnizoglu D., Usubutun A., Saatci I., Aynaci M., et al. Evaluation of 36 patients from Turkey with neuronal ceroid lipofuscinosis: clinical, neurophysiological, neuroradiological and histopathologic studies. Turk. J. Pediatr. 2004, 46:1-10.
-
(2004)
Turk. J. Pediatr.
, vol.46
, pp. 1-10
-
-
Topcu, M.1
Tan, H.2
Yalnizoglu, D.3
Usubutun, A.4
Saatci, I.5
Aynaci, M.6
-
78
-
-
8744251345
-
Hippocampal pathology in the human neuronal ceroid-lipofuscinoses: distinct patterns of storage deposition, neurodegeneration and glial activation
-
Tyynela J., Cooper J.D., Khan M.N., Shemilts S.J., Haltia M. Hippocampal pathology in the human neuronal ceroid-lipofuscinoses: distinct patterns of storage deposition, neurodegeneration and glial activation. Brain Pathol. 2004, 14:349-357.
-
(2004)
Brain Pathol.
, vol.14
, pp. 349-357
-
-
Tyynela, J.1
Cooper, J.D.2
Khan, M.N.3
Shemilts, S.J.4
Haltia, M.5
-
79
-
-
0030876737
-
EEG and evoked potentials in infantile neuronal ceroid-lipofuscinosis
-
Vanhanen S.L., Sainio K., Lappi M., Santavuori P. EEG and evoked potentials in infantile neuronal ceroid-lipofuscinosis. Dev. Med. Child Neurol. 1997, 39:456-463.
-
(1997)
Dev. Med. Child Neurol.
, vol.39
, pp. 456-463
-
-
Vanhanen, S.L.1
Sainio, K.2
Lappi, M.3
Santavuori, P.4
-
80
-
-
67649672147
-
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function
-
Vantaggiato C., Redaelli F., Falcone S., Perrotta C., Tonelli A., Bondioni S., et al. A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function. Hum. Mutat. 2009, 30:1104-1116.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 1104-1116
-
-
Vantaggiato, C.1
Redaelli, F.2
Falcone, S.3
Perrotta, C.4
Tonelli, A.5
Bondioni, S.6
-
81
-
-
63249117336
-
Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis
-
Weimer J.M., Benedict J.W., Getty A.L., Pontikis C.C., Lim M.J., Cooper J.D., et al. Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis. Brain Res. 2009, 1266:93-107.
-
(2009)
Brain Res.
, vol.1266
, pp. 93-107
-
-
Weimer, J.M.1
Benedict, J.W.2
Getty, A.L.3
Pontikis, C.C.4
Lim, M.J.5
Cooper, J.D.6
-
82
-
-
33646486569
-
Visual deficits in a mouse model of batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons
-
Weimer J.M., Custer A.W., Benedict J.W., Alexander N.A., Kingsley E., Federoff H.J., et al. Visual deficits in a mouse model of batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons. Neurobiol. Dis. 2006, 22:284-293.
-
(2006)
Neurobiol. Dis.
, vol.22
, pp. 284-293
-
-
Weimer, J.M.1
Custer, A.W.2
Benedict, J.W.3
Alexander, N.A.4
Kingsley, E.5
Federoff, H.J.6
-
83
-
-
0020376232
-
Adult ceroid-lipofuscinosis: diagnostic value of biopsies and of neurophysiological investigations
-
Vercruyssen A., Martin J.J., Ceuterick C., Jacobs K., Swerts L. Adult ceroid-lipofuscinosis: diagnostic value of biopsies and of neurophysiological investigations. J. Neurol. Neurosurg. Psychiatry 1982, 45:1056-1059.
-
(1982)
J. Neurol. Neurosurg. Psychiatry
, vol.45
, pp. 1056-1059
-
-
Vercruyssen, A.1
Martin, J.J.2
Ceuterick, C.3
Jacobs, K.4
Swerts, L.5
-
84
-
-
0029153109
-
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
-
Vesa J., Hellsten E., Verkruyse L.A., Camp L.A., Rapola J., Santavuori P., et al. Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis. Nature 1995, 376:584-587.
-
(1995)
Nature
, vol.376
, pp. 584-587
-
-
Vesa, J.1
Hellsten, E.2
Verkruyse, L.A.3
Camp, L.A.4
Rapola, J.5
Santavuori, P.6
-
85
-
-
64649097377
-
Progressive thalamocortical neuron loss in Cln5 deficient mice: distinct effects in Finnish variant late infantile NCL
-
von Schantz C., Kielar C., Hansen S.N., Pontikis C.C., Alexander N.A., Kopra O., et al. Progressive thalamocortical neuron loss in Cln5 deficient mice: distinct effects in Finnish variant late infantile NCL. Neurobiol. Dis. 2009, 34:308-319.
-
(2009)
Neurobiol. Dis.
, vol.34
, pp. 308-319
-
-
von Schantz, C.1
Kielar, C.2
Hansen, S.N.3
Pontikis, C.C.4
Alexander, N.A.5
Kopra, O.6
-
86
-
-
34249877686
-
A novel mutation of the CLN8 gene: is there a Mediterranean phenotype?
-
Zelnik N., Mahajna M., Iancu T.C., Sharony R., Zeigler M. A novel mutation of the CLN8 gene: is there a Mediterranean phenotype?. Pediatr. Neurol. 2007, 36:411-413.
-
(2007)
Pediatr. Neurol.
, vol.36
, pp. 411-413
-
-
Zelnik, N.1
Mahajna, M.2
Iancu, T.C.3
Sharony, R.4
Zeigler, M.5
-
87
-
-
33747890559
-
The brain as a target of inflammation: common pathways link inflammatory and neurodegenerative diseases
-
Zipp F., Aktas O. The brain as a target of inflammation: common pathways link inflammatory and neurodegenerative diseases. Trends Neurosci. 2006, 29:518-527.
-
(2006)
Trends Neurosci.
, vol.29
, pp. 518-527
-
-
Zipp, F.1
Aktas, O.2
|