-
1
-
-
0027180961
-
Leber's hereditary optic neuropathy: New genetic considerations
-
Newman NJ: Leber's hereditary optic neuropathy: New genetic considerations. Arch Neurol 1993;50:540-548.
-
(1993)
Arch Neurol
, vol.50
, pp. 540-548
-
-
Newman, N.J.1
-
2
-
-
0020602931
-
Ophthalmological findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members
-
Nikoskelainen E, Hyot WF, Nummelin K: Ophthalmological findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members. Arch Ophthalmol 1983;101:1059-1068.
-
(1983)
Arch Ophthalmol
, vol.101
, pp. 1059-1068
-
-
Nikoskelainen, E.1
Hyot, W.F.2
Nummelin, K.3
-
3
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AMS, Elsas IJ II, Nikoskelainen EK: Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 1988;242:1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.S.6
Elsas I.J. II7
Nikoskelainen, E.K.8
-
4
-
-
0025944560
-
Leber hereditary optic neuropathy: Identification of the same mitochondrial ND1 mutation in six pedigrees
-
Howell N, Bindoff LA, McCullough DA, Kubacka I, Poulton J, Mackey DA, Taylor L, Turnbull DM: Leber hereditary optic neuropathy: Identification of the same mitochondrial ND1 mutation in six pedigrees. Am J Hum Genet 1991;49:939-950.
-
(1991)
Am J Hum Genet
, vol.49
, pp. 939-950
-
-
Howell, N.1
Bindoff, L.A.2
McCullough, D.A.3
Kubacka, I.4
Poulton, J.5
Mackey, D.A.6
Taylor, L.7
Turnbull, D.M.8
-
5
-
-
0025910614
-
A new mtDNA mutation associated with Leber's hereditary optic neuropathy
-
Huoponen K, Vilkki J, Aula P, Nikoskelainen E, Savontaus ML: A new mtDNA mutation associated with Leber's hereditary optic neuropathy. Am J Hum Genet 1991;48:1147-1153.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 1147-1153
-
-
Huoponen, K.1
Vilkki, J.2
Aula, P.3
Nikoskelainen, E.4
Savontaus, M.L.5
-
6
-
-
0026746739
-
A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by unusual mitochondrial genetic etiology
-
Mackey DA, Howell N: A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by unusual mitochondrial genetic etiology. Am J Hum Genet 1992; 51:1218-1228.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1218-1228
-
-
Mackey, D.A.1
Howell, N.2
-
8
-
-
0029816017
-
Primary pathogenic mtDNA mutations in multigeneration pedigree with Leber hereditary optic neuropathy
-
Mackey DA, Oostra RJ, Rosenberg T, Nikoskelainen E, Bronte-Stewart J, Poulton J, Harding AE, Govan G, Bolhuis PA, Norby S: Primary pathogenic mtDNA mutations in multigeneration pedigree with Leber hereditary optic neuropathy. Am J Hum Genet 1996;59:481-485.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 481-485
-
-
Mackey, D.A.1
Oostra, R.J.2
Rosenberg, T.3
Nikoskelainen, E.4
Bronte-Stewart, J.5
Poulton, J.6
Harding, A.E.7
Govan, G.8
Bolhuis, P.A.9
Norby, S.10
-
9
-
-
0001174007
-
Leber's optic atrophy and its relationship with heredo-familial ataxias
-
Ferguson FR, Critchley M: Leber's optic atrophy and its relationship with heredo-familial ataxias. J Neurol Psychopathol 1928;9:120-132.
-
(1928)
J Neurol Psychopathol
, vol.9
, pp. 120-132
-
-
Ferguson, F.R.1
Critchley, M.2
-
10
-
-
0002387271
-
Leber's disease: A genealogic, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families
-
Lundsgaard R: Leber's disease: A genealogic, genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families. Acta Ophthalmol 1944;21(suppl):37-157.
-
(1944)
Acta Ophthalmol
, vol.21
, Issue.SUPPL.
, pp. 37-157
-
-
Lundsgaard, R.1
-
12
-
-
0026782507
-
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial mutation
-
Harding AE, Sweeney MG, Miller DH, Mumford CJ, Kellar-Wood H, Menard D, McDonald WI, Compston DAS: Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial mutation. Brain 1992;115:979-989.
-
(1992)
Brain
, vol.115
, pp. 979-989
-
-
Harding, A.E.1
Sweeney, M.G.2
Miller, D.H.3
Mumford, C.J.4
Kellar-Wood, H.5
Menard, D.6
McDonald, W.I.7
Compston, D.A.S.8
-
13
-
-
0001072895
-
The use of confidence or fiducial limits illustrated in the case of the binominal
-
Clopper CJ, Pearson ES: The use of confidence or fiducial limits illustrated in the case of the binominal. Biometrika 1934;26:404.
-
(1934)
Biometrika
, vol.26
, pp. 404
-
-
Clopper, C.J.1
Pearson, E.S.2
-
14
-
-
0027731794
-
Association of the 11778 mitochondrial DNA mutations and demyelinating disease
-
Flanigan KM, Johns DR: Association of the 11778 mitochondrial DNA mutations and demyelinating disease. Neurology 1993;43:2720-2722.
-
(1993)
Neurology
, vol.43
, pp. 2720-2722
-
-
Flanigan, K.M.1
Johns, D.R.2
-
15
-
-
0028337837
-
Leber's hereditary optic neuropathy mitochondrial mutations in multiple sclerosis
-
Kellar-Wood H, Robertson N, Govan GG, Compston DAS. Harding AE: Leber's hereditary optic neuropathy mitochondrial mutations in multiple sclerosis. Ann Neurol 1994;36:109-112.
-
(1994)
Ann Neurol
, vol.36
, pp. 109-112
-
-
Kellar-Wood, H.1
Robertson, N.2
Govan, G.G.3
Compston, D.A.S.4
Harding, A.E.5
-
16
-
-
0028595987
-
Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis
-
Hanefeld FA, Ernst BP, Wilichowski E, Christen H-J: Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis. Neuropediatrics 1994;25: 331.
-
(1994)
Neuropediatrics
, vol.25
, pp. 331
-
-
Hanefeld, F.A.1
Ernst, B.P.2
Wilichowski, E.3
Christen, H.-J.4
-
17
-
-
0029153643
-
No association of the 11778 mitochondrial DNA mutations and multiple sclerosis in Japan
-
Nishimura M, Obayashi H, Ohta M, Uchiyama T, Hao Q. Saida T: No association of the 11778 mitochondrial DNA mutations and multiple sclerosis in Japan. Neurology 1995;45:1333-1334.
-
(1995)
Neurology
, vol.45
, pp. 1333-1334
-
-
Nishimura, M.1
Obayashi, H.2
Ohta, M.3
Uchiyama, T.4
Hao, Q.5
Saida, T.6
-
18
-
-
0029759665
-
Mitochondrial DNA mutations in mutliple sclerosis patients with severe optic involvement
-
Mayr-Wohlfart U, Paulus C, Henneberg A, Rödel G: Mitochondrial DNA mutations in mutliple sclerosis patients with severe optic involvement. Acta Neurol Scand 1996;94:167-171.
-
(1996)
Acta Neurol Scand
, vol.94
, pp. 167-171
-
-
Mayr-Wohlfart, U.1
Paulus, C.2
Henneberg, A.3
Rödel, G.4
-
19
-
-
0029279163
-
Mitochondrial DNA mutations in multiple sclerosis
-
Kalman , Lublin FD, Alder H: Mitochondrial DNA mutations in multiple sclerosis. Multiple Sclerosis 1995;1:32-36.
-
(1995)
Multiple Sclerosis
, vol.1
, pp. 32-36
-
-
Kalman1
Lublin, F.D.2
Alder, H.3
-
21
-
-
0019406639
-
The incidence and prevalence of reported multiple sclerosis
-
Baum HM, Rothschild BB: The incidence and prevalence of reported multiple sclerosis. Ann-Neurol 1981;10:420-428.
-
(1981)
Ann-Neurol
, vol.10
, pp. 420-428
-
-
Baum, H.M.1
Rothschild, B.B.2
-
22
-
-
0026989344
-
Leber hereditary optic neuropathy in Australia
-
Mackey DA, Buttery RG: Leber hereditary optic neuropathy in Australia. Aust NZ J Ophthalmol 1992;20:177-184.
-
(1992)
Aust NZ J Ophthalmol
, vol.20
, pp. 177-184
-
-
Mackey, D.A.1
Buttery, R.G.2
|