-
1
-
-
0033678145
-
Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease
-
Cailloux F, Gauthier-Barichard F, Mimault C, et al. Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease. Eur J Hum Genet 2000; 8: 837–45.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 837-845
-
-
Cailloux, F.1
Gauthier-Barichard, F.2
Mimault, C.3
-
2
-
-
77957688535
-
Magnetic resonance imaging pattern recognition in hypomyelinating disorders
-
Steenweg ME, Vanderver A, Blaser S, et al. Magnetic resonance imaging pattern recognition in hypomyelinating disorders. Brain 2010; 133: 2971–82.
-
(2010)
Brain
, vol.133
, pp. 2971-2982
-
-
Steenweg, M.E.1
Vanderver, A.2
Blaser, S.3
-
3
-
-
0001790128
-
Myelination and retarded myelination
-
In, van der Knaap MS, Valk J, editors., Berlin, Springer-Verlag
-
van der Knaap MS, Valk J. Myelination and retarded myelination. In: van der Knaap MS, Valk J, editors. Magnetic Resonance of Myelin, Myelination, and Myelin Disorders. Berlin: Springer-Verlag, 1995: 31–52.
-
(1995)
Magnetic Resonance of Myelin, Myelination, and Myelin Disorders
, pp. 31-52
-
-
van der Knaap, M.S.1
Valk, J.2
-
4
-
-
0031953422
-
An MRI and MRS study of Pelizaeus-Merzbacher disease
-
Nezu A, Kimura S, Takeshita S, et al. An MRI and MRS study of Pelizaeus-Merzbacher disease. Pediatr Neurol 1998; 18: 334–37.
-
(1998)
Pediatr Neurol
, vol.18
, pp. 334-337
-
-
Nezu, A.1
Kimura, S.2
Takeshita, S.3
-
5
-
-
0032692761
-
MR-revealed myelination in the cerebral corticospinal tract as a marker for Pelizaeus-Merzbacher's disease with proteolipid protein gene duplication
-
Takanashi J, Sugita K, Tanabe Y, et al. MR-revealed myelination in the cerebral corticospinal tract as a marker for Pelizaeus-Merzbacher's disease with proteolipid protein gene duplication. Am J Neuroradiol 1999; 20: 1822–28.
-
(1999)
Am J Neuroradiol
, vol.20
, pp. 1822-1828
-
-
Takanashi, J.1
Sugita, K.2
Tanabe, Y.3
-
6
-
-
0042233990
-
Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus-Merzbacher phenotype
-
Plecko B, Stöckler-Ipsiroglu S, Gruber S, et al. Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus-Merzbacher phenotype. Neuropediatrics 2003; 34: 127–36.
-
(2003)
Neuropediatrics
, vol.34
, pp. 127-136
-
-
Plecko, B.1
Stöckler-Ipsiroglu, S.2
Gruber, S.3
-
7
-
-
84867472678
-
Neural stem cell engraftment and myelination in the human brain
-
Gupta N, Henry RG, Strober J, et al. Neural stem cell engraftment and myelination in the human brain. Sci Transl Med 2012; 4: 155ra137.
-
(2012)
Sci Transl Med
, vol.4
, pp. 155ra137
-
-
Gupta, N.1
Henry, R.G.2
Strober, J.3
-
9
-
-
84888137920
-
Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher disease
-
Laukka JJ, Stanley JA, Garbern JY, et al. Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher disease. J Neurol Sci 2013; 335: 75–81.
-
(2013)
J Neurol Sci
, vol.335
, pp. 75-81
-
-
Laukka, J.J.1
Stanley, J.A.2
Garbern, J.Y.3
-
10
-
-
15444363703
-
PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2
-
Inoue K. PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Neurogenetics 2005; 6: 1–16.
-
(2005)
Neurogenetics
, vol.6
, pp. 1-16
-
-
Inoue, K.1
-
11
-
-
0025031812
-
No adjustments are needed for multiple comparisons
-
Rothman KJ. No adjustments are needed for multiple comparisons. Epidemiology 1990; 1: 43–46.
-
(1990)
Epidemiology
, vol.1
, pp. 43-46
-
-
Rothman, K.J.1
-
12
-
-
3342943178
-
Do multiple outcome measures require p-value adjustment?
-
Feise RJ. Do multiple outcome measures require p-value adjustment? BMC Med Res Methodol 2002; 2: 8.
-
(2002)
BMC Med Res Methodol
, vol.2
, pp. 8
-
-
Feise, R.J.1
-
13
-
-
0028926516
-
Neurophysiologic studies and MRI in Pelizaeus-Merzbacher disease: comparison of classic and connatal forms
-
Wang PJ, Young C, Liu HM, et al. Neurophysiologic studies and MRI in Pelizaeus-Merzbacher disease: comparison of classic and connatal forms. Pediatr Neurol 1995; 12: 47–53.
-
(1995)
Pediatr Neurol
, vol.12
, pp. 47-53
-
-
Wang, P.J.1
Young, C.2
Liu, H.M.3
-
14
-
-
84893003219
-
Further genotype-phenotype correlation emerging from two families with PLP1 exon 4 skipping
-
Biancheri R, Grossi S, Regis S, et al. Further genotype-phenotype correlation emerging from two families with PLP1 exon 4 skipping. Clin Genet 2014; 85: 267–72.
-
(2014)
Clin Genet
, vol.85
, pp. 267-272
-
-
Biancheri, R.1
Grossi, S.2
Regis, S.3
-
15
-
-
69949177941
-
Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1
-
Sima AA, Pierson CR, Woltjer RL, et al. Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1. Acta Neuropathol 2009; 118: 531–39.
-
(2009)
Acta Neuropathol
, vol.118
, pp. 531-539
-
-
Sima, A.A.1
Pierson, C.R.2
Woltjer, R.L.3
-
16
-
-
0036189424
-
Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation
-
Garbern JY, Yool DA, Moore GJ, et al. Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. Brain 2002; 125: 551–61.
-
(2002)
Brain
, vol.125
, pp. 551-561
-
-
Garbern, J.Y.1
Yool, D.A.2
Moore, G.J.3
-
17
-
-
0037444675
-
Proteolipid protein gene mutation induces altered ventilatory response to hypoxia in the myelin-deficient rat
-
Miller MJ, Haxhiu MA, Georgiadis P, et al. Proteolipid protein gene mutation induces altered ventilatory response to hypoxia in the myelin-deficient rat. J Neurosci 2003; 23: 2265–73.
-
(2003)
J Neurosci
, vol.23
, pp. 2265-2273
-
-
Miller, M.J.1
Haxhiu, M.A.2
Georgiadis, P.3
-
18
-
-
33646267186
-
Processing of PLP in a model of Pelizaeus-Merzbacher disease/SPG2 due to the rumpshaker mutation
-
McLaughlin M, Barrie JA, Karim S, et al. Processing of PLP in a model of Pelizaeus-Merzbacher disease/SPG2 due to the rumpshaker mutation. Glia 2006; 53: 715–22.
-
(2006)
Glia
, vol.53
, pp. 715-722
-
-
McLaughlin, M.1
Barrie, J.A.2
Karim, S.3
-
19
-
-
0032543261
-
Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene
-
Anderson TJ, Schneider A, Barrie JA, et al. Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene. J Comp Neurol 1998; 394: 506–19.
-
(1998)
J Comp Neurol
, vol.394
, pp. 506-519
-
-
Anderson, T.J.1
Schneider, A.2
Barrie, J.A.3
-
20
-
-
0033216282
-
Identification of a new exon in the myelin proteolipid protein gene encoding novel protein isoforms that are restricted to the somata of oligodendrocytes and neurons
-
Bongarzone ER, Campagnoni CW, Kampf K, et al. Identification of a new exon in the myelin proteolipid protein gene encoding novel protein isoforms that are restricted to the somata of oligodendrocytes and neurons. J Neurosci 1999; 19: 8349–57.
-
(1999)
J Neurosci
, vol.19
, pp. 8349-8357
-
-
Bongarzone, E.R.1
Campagnoni, C.W.2
Kampf, K.3
-
21
-
-
77951929119
-
Novel neuronal proteolipid protein isoforms encoded by the human myelin proteolipid protein 1 gene
-
Sarret C, Combes P, Micheau P, et al. Novel neuronal proteolipid protein isoforms encoded by the human myelin proteolipid protein 1 gene. Neuroscience 2010; 166: 522–38.
-
(2010)
Neuroscience
, vol.166
, pp. 522-538
-
-
Sarret, C.1
Combes, P.2
Micheau, P.3
-
22
-
-
84865224816
-
Determination of cerebellar volume in children and adolescents with magnetic resonance images
-
Kosar MI, Karacan K, Otag I, et al. Determination of cerebellar volume in children and adolescents with magnetic resonance images. Folia Morphol 2012; 71: 65–70.
-
(2012)
Folia Morphol
, vol.71
, pp. 65-70
-
-
Kosar, M.I.1
Karacan, K.2
Otag, I.3
|