-
1
-
-
0030962978
-
MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type
-
Autti T., Raininko R., Santavuori P., Vanhanen S.L., Poutanen V.P., and Haltia M. MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type. Neuroradiology 39 (1997) 371-377
-
(1997)
Neuroradiology
, vol.39
, pp. 371-377
-
-
Autti, T.1
Raininko, R.2
Santavuori, P.3
Vanhanen, S.L.4
Poutanen, V.P.5
Haltia, M.6
-
2
-
-
34447100391
-
Decreased T2 signal in the thalami may be a sign of lysosomal storage disease
-
Autti T., Joensuu R., and Aberg L. Decreased T2 signal in the thalami may be a sign of lysosomal storage disease. Neuroradiology 49 (2007) 571-578
-
(2007)
Neuroradiology
, vol.49
, pp. 571-578
-
-
Autti, T.1
Joensuu, R.2
Aberg, L.3
-
3
-
-
2942597781
-
Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 (PPT1) null mutant mouse model of infantile neuronal ceroid lipofuscinosis
-
Bible E., Gupta P., Hofmann S.L., and Cooper J.D. Regional and cellular neuropathology in the palmitoyl protein thioesterase-1 (PPT1) null mutant mouse model of infantile neuronal ceroid lipofuscinosis. Neurobiol. Dis. 16 (2004) 346-359
-
(2004)
Neurobiol. Dis.
, vol.16
, pp. 346-359
-
-
Bible, E.1
Gupta, P.2
Hofmann, S.L.3
Cooper, J.D.4
-
5
-
-
0037399422
-
Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosis
-
Cooper J.D. Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosis. Curr. Opin. Neurol. 16 (2003) 121-128
-
(2003)
Curr. Opin. Neurol.
, vol.16
, pp. 121-128
-
-
Cooper, J.D.1
-
6
-
-
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., and 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. 19 (1999) 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
-
7
-
-
33750976371
-
Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis
-
Cooper J.D., Russell C., and Mitchison H.M. Progress towards understanding disease mechanisms in small vertebrate models of neuronal ceroid lipofuscinosis. Biochim. Biophys. Acta 1762 (2006) 873-889
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 873-889
-
-
Cooper, J.D.1
Russell, C.2
Mitchison, H.M.3
-
8
-
-
0037107348
-
Cln3Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth
-
Cotman S.L., Vrbanac V., Lebel L.A., Lee R.L., Johnson K.A., Donahue L.R., Teed A.M., Antonellis K., Bronson R.T., Lerner T.J., and MacDonald M.E. Cln3Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth. Hum. Mol. Genet. 11 (2002) 2709-2721
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2709-2721
-
-
Cotman, S.L.1
Vrbanac, V.2
Lebel, L.A.3
Lee, R.L.4
Johnson, K.A.5
Donahue, L.R.6
Teed, A.M.7
Antonellis, K.8
Bronson, R.T.9
Lerner, T.J.10
MacDonald, M.E.11
-
9
-
-
38149082550
-
A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3
-
Frugier T., Mitchell N.L., Tammen I., Houweling P.J., Arthur D.G., Kay G.W., van Diggelen O.P., Jolly R.D., and Palmer D.N. A new large animal model of CLN5 neuronal ceroid lipofuscinosis in Borderdale sheep is caused by a nucleotide substitution at a consensus splice site (c.571+1G>A) leading to excision of exon 3. Neurobiol. Dis. 29 (2008) 306-315
-
(2008)
Neurobiol. Dis.
, vol.29
, pp. 306-315
-
-
Frugier, T.1
Mitchell, N.L.2
Tammen, I.3
Houweling, P.J.4
Arthur, D.G.5
Kay, G.W.6
van Diggelen, O.P.7
Jolly, R.D.8
Palmer, D.N.9
-
10
-
-
84985280160
-
The efficiency of systematic sampling in stereology and its prediction
-
Gundersen H.J., and Jensen E.B. The efficiency of systematic sampling in stereology and its prediction. J. Microsc. 147 (1987) 229-263
-
(1987)
J. Microsc.
, vol.147
, pp. 229-263
-
-
Gundersen, H.J.1
Jensen, E.B.2
-
11
-
-
0035923662
-
Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice
-
Gupta P., Soyombo A.A., Atashband A., Wisniewski K.E., Shelton J.M., Richardson J.A., Hammer R.E., and Hofmann S.L. Disruption of PPT1 or PPT2 causes neuronal ceroid lipofuscinosis in knockout mice. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 13566-13571
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 13566-13571
-
-
Gupta, P.1
Soyombo, A.A.2
Atashband, A.3
Wisniewski, K.E.4
Shelton, J.M.5
Richardson, J.A.6
Hammer, R.E.7
Hofmann, S.L.8
-
12
-
-
0037226939
-
The neuronal ceroid-lipofuscinoses
-
Haltia M. The neuronal ceroid-lipofuscinoses. J. Neuropathol. Exp. Neurol. 62 (2003) 1-13
-
(2003)
J. Neuropathol. Exp. Neurol.
, vol.62
, pp. 1-13
-
-
Haltia, M.1
-
13
-
-
0033774798
-
CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain
-
Heinonen O., Salonen T., Jalanko A., Peltonen L., and Copp A. CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain. J. Comp. Neurol. 426 (2000) 406-412
-
(2000)
J. Comp. Neurol.
, vol.426
, pp. 406-412
-
-
Heinonen, O.1
Salonen, T.2
Jalanko, A.3
Peltonen, L.4
Copp, A.5
-
14
-
-
2342599787
-
The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain.
-
Holmberg V., Jalanko A., Isosomppi J., Fabritius A.L., Peltonen L., and Kopra O. The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain. Neurobiol. Dis. 16 (2004) 29-40
-
(2004)
Neurobiol. Dis.
, vol.16
, pp. 29-40
-
-
Holmberg, V.1
Jalanko, A.2
Isosomppi, J.3
Fabritius, A.L.4
Peltonen, L.5
Kopra, O.6
-
15
-
-
0037091074
-
Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein
-
Isosomppi J., Vesa J., Jalanko A., and Peltonen L. Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein. Hum. Mol. Genet. 11 (2002) 885-891
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 885-891
-
-
Isosomppi, J.1
Vesa, J.2
Jalanko, A.3
Peltonen, L.4
-
16
-
-
11844286979
-
Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons
-
Δex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons. Neurobiol. Dis. 18 (2005) 226-241
-
(2005)
Neurobiol. Dis.
, vol.18
, pp. 226-241
-
-
Jalanko, A.1
Vesa, J.2
Manninen, T.3
von Schantz, C.4
Minye, H.5
Fabritius, A.L.6
Salonen, T.7
Rapola, J.8
Gentile, M.9
Kopra, O.10
Peltonen, L.11
-
17
-
-
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., McCauley S.L., Griffey M.A., Wong M., Sands M.S., and Cooper J.D. Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosis. Neurobiol. Dis. 25 (2007) 150-162
-
(2007)
Neurobiol. Dis.
, vol.25
, pp. 150-162
-
-
Kielar, C.1
Maddox, L.2
Bible, E.3
Pontikis, C.C.4
McCauley, S.L.5
Griffey, M.A.6
Wong, M.7
Sands, M.S.8
Cooper, J.D.9
-
18
-
-
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., and Mukherjee A.B. Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice. J. Clin. Invest. 118 (2008) 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
Mukherjee, A.B.7
-
19
-
-
9744278990
-
A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging
-
Kopra O., Vesa J., von Schantz C., Manninen T., Minye H., Fabritius A.L., Rapola J., van Diggelen O.P., Saarela J., Jalanko A., and Peltonen L. A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging. Hum. Mol. Genet. 13 (2004) 2893-2906
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2893-2906
-
-
Kopra, O.1
Vesa, J.2
von Schantz, C.3
Manninen, T.4
Minye, H.5
Fabritius, A.L.6
Rapola, J.7
van Diggelen, O.P.8
Saarela, J.9
Jalanko, A.10
Peltonen, L.11
-
20
-
-
25844517550
-
Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses
-
Mole S.E., Williams R.E., and Goebel H.H. Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses. Neurogenetics 6 (2005) 107-126
-
(2005)
Neurogenetics
, vol.6
, pp. 107-126
-
-
Mole, S.E.1
Williams, R.E.2
Goebel, H.H.3
-
21
-
-
0032744277
-
Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten mouse model consortium
-
Mitchison H.M., Bernard D.J., Greene N.D.E., Cooper J.D., Junaid M.A., Pullarkat R.K., Vos N., Breuning M.H., Owens J.W., Mobley W.C., Gardiner R.M., Lake B.D., Taschner P.E.M., and Nussbaum R.L. Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten mouse model consortium. Neurobiol. Dis. 6 (1999) 321-334
-
(1999)
Neurobiol. Dis.
, vol.6
, pp. 321-334
-
-
Mitchison, H.M.1
Bernard, D.J.2
Greene, N.D.E.3
Cooper, J.D.4
Junaid, M.A.5
Pullarkat, R.K.6
Vos, N.7
Breuning, M.H.8
Owens, J.W.9
Mobley, W.C.10
Gardiner, R.M.11
Lake, B.D.12
Taschner, P.E.M.13
Nussbaum, R.L.14
-
22
-
-
1042276701
-
Selectivity and types of cell death in the neuronal ceroid lipofuscinoses.
-
Mitchison H.M., Lim M.J., and Cooper J.D. Selectivity and types of cell death in the neuronal ceroid lipofuscinoses. Brain Pathol. 14 (2004) 86-96
-
(2004)
Brain Pathol.
, vol.14
, pp. 86-96
-
-
Mitchison, H.M.1
Lim, M.J.2
Cooper, J.D.3
-
23
-
-
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.A., Rezaie P., and Cooper J.D. Glial activation spreads from specific cerebral foci and precedes neurodegeneration in presymptomatic ovine neuronal ceroid lipofuscinosis (CLN6). Neurobiol. Dis. 20 (2005) 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.A.4
Rezaie, P.5
Cooper, J.D.6
-
24
-
-
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., Saftig P., Gillingwater T.H., Cooper J.D., and Tyynelä J. Synaptic changes in the thalamocortical system of cathepsin D-deficient mice: a model of human congenital neuronal ceroid-lipofuscinosis. J. Neuropathol. Exp. Neurol. 67 (2008) 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
Saftig, P.7
Gillingwater, T.H.8
Cooper, J.D.9
Tyynelä, J.10
-
26
-
-
4544285361
-
-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation
-
-/- mouse model of juvenile neuronal ceroid lipofuscinosis is preceded by low level glial activation. Brain Res. 1023 (2004) 231-242
-
(2004)
Brain Res.
, vol.1023
, pp. 231-242
-
-
Pontikis, C.C.1
Cella, C.V.2
Parihar, N.3
Lim, M.J.4
Chakrabarti, S.5
Mitchison, H.M.6
Mobley, W.C.7
Rezaie, P.8
Pearce, D.A.9
Cooper, J.D.10
-
28
-
-
0032814562
-
Neuroglial activation repertoire in the injured brain: graded response, molecular mechanisms and cues to physiological function
-
Raivich G., Bohatschek M., Kloss C.U., Werner A., Jones L.L., and Kreutzberg G.W. Neuroglial activation repertoire in the injured brain: graded response, molecular mechanisms and cues to physiological function. Brain Res. 30 (1999) 77-105
-
(1999)
Brain Res.
, vol.30
, pp. 77-105
-
-
Raivich, G.1
Bohatschek, M.2
Kloss, C.U.3
Werner, A.4
Jones, L.L.5
Kreutzberg, G.W.6
-
29
-
-
0023917534
-
Neuronal ceroid-lipofuscinoses in childhood
-
Santavuori P. Neuronal ceroid-lipofuscinoses in childhood. Brain Dev. 10 (1988) 80-83
-
(1988)
Brain Dev.
, vol.10
, pp. 80-83
-
-
Santavuori, P.1
-
31
-
-
0027279119
-
Early juvenile neuronal ceroid-lipofuscinosis or variant Jansky-Bielschowsky disease: diagnostic criteria and nomenclature
-
Santavuori P., Rapola J., Raininko R., Autti T., Lappi M., Nuutila A., Launes J., and Sainio K. Early juvenile neuronal ceroid-lipofuscinosis or variant Jansky-Bielschowsky disease: diagnostic criteria and nomenclature. J. Inherit. Metab. Dis. 16 (1993) 230-232
-
(1993)
J. Inherit. Metab. Dis.
, vol.16
, pp. 230-232
-
-
Santavuori, P.1
Rapola, J.2
Raininko, R.3
Autti, T.4
Lappi, M.5
Nuutila, A.6
Launes, J.7
Sainio, K.8
-
32
-
-
33750984767
-
Molecular genetics of the NCLs - status and perspectives
-
Siintola E., Lehesjoki A.E., and Mole S.E. Molecular genetics of the NCLs - status and perspectives. Biochim. Biophys. Acta 1762 (2006) 857-864
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 857-864
-
-
Siintola, E.1
Lehesjoki, A.E.2
Mole, S.E.3
-
33
-
-
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., Liu X.Q., Wilson C., Lahtinen U., Anttonen A.K., and Lehesjoki A.E. The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter. Am. J. Hum. Genet. 81 (2007) 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
Liu, X.Q.7
Wilson, C.8
Lahtinen, U.9
Anttonen, A.K.10
Lehesjoki, A.E.11
-
34
-
-
5644241723
-
A mouse model of classical late-infantile neuronal ceroid lipofuscinosis based on targeted disruption of the CLN2 gene results in a loss of tripeptidyl-peptidase I activity and progressive neurodegeneration
-
Sleat D.E., Wiseman J.A., El-Banna M., Kim K.H., Mao Q., Price S., Macauley S.L., Sidman R.L., Shen M.M., Zhao Q., Passini M.A., Davidson B.L., Stewart G.R., and Lobel P. A mouse model of classical late-infantile neuronal ceroid lipofuscinosis based on targeted disruption of the CLN2 gene results in a loss of tripeptidyl-peptidase I activity and progressive neurodegeneration. J. Neurosci. 24 (2004) 9117-9126
-
(2004)
J. Neurosci.
, vol.24
, pp. 9117-9126
-
-
Sleat, D.E.1
Wiseman, J.A.2
El-Banna, M.3
Kim, K.H.4
Mao, Q.5
Price, S.6
Macauley, S.L.7
Sidman, R.L.8
Shen, M.M.9
Zhao, Q.10
Passini, M.A.11
Davidson, B.L.12
Stewart, G.R.13
Lobel, P.14
-
35
-
-
17844387148
-
The human brain mannose 6-phosphate glycoproteome: a complex mixture composed of multiple isoforms of many soluble lysosomal proteins
-
Sleat D.E., Lackland H., Wang Y., Sohar I., Xiao G., Li H., and Lobel P. The human brain mannose 6-phosphate glycoproteome: a complex mixture composed of multiple isoforms of many soluble lysosomal proteins. Proteomics 5 (2005) 1520-1532
-
(2005)
Proteomics
, vol.5
, pp. 1520-1532
-
-
Sleat, D.E.1
Lackland, H.2
Wang, Y.3
Sohar, I.4
Xiao, G.5
Li, H.6
Lobel, P.7
-
36
-
-
8744251345
-
Specific patterns of storage deposition, neurodegeneration, and glial activation in the hippocampus of patients with neuronal ceroid-lipofuscinoses
-
Tyynelä J., Cooper J.D., Khan M.N., Shemilt S.J.A., and Haltia M. Specific patterns of storage deposition, neurodegeneration, and glial activation in the hippocampus of patients with neuronal ceroid-lipofuscinoses. Brain Pathol. 14 (2004) 349-357
-
(2004)
Brain Pathol.
, vol.14
, pp. 349-357
-
-
Tyynelä, J.1
Cooper, J.D.2
Khan, M.N.3
Shemilt, S.J.A.4
Haltia, M.5
-
37
-
-
0036326358
-
Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3
-
Vesa J., Chin M.H., Oelgeschlager K., Isosomppi J., DellAngelica E.C., Jalanko A., and Peltonen L. Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3. Mol. Biol. Cell 13 (2002) 2410-2420
-
(2002)
Mol. Biol. Cell
, vol.13
, pp. 2410-2420
-
-
Vesa, J.1
Chin, M.H.2
Oelgeschlager, K.3
Isosomppi, J.4
DellAngelica, E.C.5
Jalanko, A.6
Peltonen, L.7
-
38
-
-
0031942743
-
Microglia and the development of spongiform change in Creutzfeldt-Jakob disease
-
von Eitzen U., Egensperger R., Kosel S., Grasbon-Frodl E.M., Imai Y., Bise K., Kohsaka S., Mehraein P., and Graeber M.B. Microglia and the development of spongiform change in Creutzfeldt-Jakob disease. J. Neuropathol. Exp. Neurol. 57 (1998) 246-256
-
(1998)
J. Neuropathol. Exp. Neurol.
, vol.57
, pp. 246-256
-
-
von Eitzen, U.1
Egensperger, R.2
Kosel, S.3
Grasbon-Frodl, E.M.4
Imai, Y.5
Bise, K.6
Kohsaka, S.7
Mehraein, P.8
Graeber, M.B.9
-
39
-
-
43449115394
-
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases
-
von Schantz C., Saharinen J., Kopra O., Cooper J.D., Gentile M., Hovatta I., Peltonen L., and Jalanko A. Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases. BMC Genomics 9 (2008) 146
-
(2008)
BMC Genomics
, vol.9
, pp. 146
-
-
von Schantz, C.1
Saharinen, J.2
Kopra, O.3
Cooper, J.D.4
Gentile, M.5
Hovatta, I.6
Peltonen, L.7
Jalanko, A.8
-
40
-
-
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., Cooper J.D., and Pearce D.A. 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. 22 (2006) 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
Cooper, J.D.7
Pearce, D.A.8
|