-
1
-
-
0032865035
-
Clinical nosologic and genetic aspects of Joubert and related syndromes
-
Chance PF, Cavalier L, Satran D, et al: Clinical nosologic and genetic aspects of Joubert and related syndromes. J Child Neurol 1999;14:660-666.
-
(1999)
J. Child Neurol.
, vol.14
, pp. 660-666
-
-
Chance, P.F.1
Cavalier, L.2
Satran, D.3
-
3
-
-
0033615477
-
Cerebello-oculo-renal syndromes including Arima, Senior-Loken and COACH syndromes: More than just variants of Joubert syndrome
-
Satran D, Pierpont ME, Dobyns WB: Cerebello-oculo-renal syndromes including Arima, Senior-Loken and COACH syndromes: More than just variants of Joubert syndrome. Am J Med Genet 1999;86:459-469.
-
(1999)
Am. J. Med. Genet.
, vol.86
, pp. 459-469
-
-
Satran, D.1
Pierpont, M.E.2
Dobyns, W.B.3
-
4
-
-
0031438402
-
"Joubert syndrome" revisited: Key ocular motor signs with magnetic resonance imaging correlation
-
Maria BL, Hoang KB, Tusa RJ, et al: "Joubert syndrome" revisited: Key ocular motor signs with magnetic resonance imaging correlation. J Child Neurol 1997;12:423-430.
-
(1997)
J. Child Neurol.
, vol.12
, pp. 423-430
-
-
Maria, B.L.1
Hoang, K.B.2
Tusa, R.J.3
-
5
-
-
0032989288
-
Molar tooth sign in Joubert syndrome: Clinical, radiologic, and pathologic significance
-
Maria BL, Quisling RG, Rosainz LC, et al: Molar tooth sign in Joubert syndrome: Clinical, radiologic, and pathologic significance. J Child Neurol 1999;14:368-376.
-
(1999)
J. Child Neurol.
, vol.14
, pp. 368-376
-
-
Maria, B.L.1
Quisling, R.G.2
Rosainz, L.C.3
-
6
-
-
0033358738
-
Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity
-
Saar K, Al-Gazali L, Sztriha L, et al: Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity. Am J Hum Genet 1999; 65:1666-1671.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1666-1671
-
-
Saar, K.1
Al-Gazali, L.2
Sztriha, L.3
-
7
-
-
0018079385
-
Uncommon syndromes of cerebellar vermis aplasia. I: Joubert syndrome
-
Friede RL, Boltshauser E: Uncommon syndromes of cerebellar vermis aplasia. I: Joubert syndrome. Dev Med Child Neurol 1978;20: 758-763.
-
(1978)
Dev. Med. Child Neurol.
, vol.20
, pp. 758-763
-
-
Friede, R.L.1
Boltshauser, E.2
-
8
-
-
0032833614
-
Neuropathology of Joubert syndrome
-
Yachnis AT, Rorke LB: Neuropathology of Joubert syndrome. J Child Neurol 1999;14:655-659.
-
(1999)
J. Child Neurol.
, vol.14
, pp. 655-659
-
-
Yachnis, A.T.1
Rorke, L.B.2
-
10
-
-
0029410597
-
MR imaging of Joubert's syndrome
-
Sener RN: MR imaging of Joubert's syndrome. Comput Med Imaging Graph 1995;19:481-486.
-
(1995)
Comput. Med. Imaging Graph
, vol.19
, pp. 481-486
-
-
Sener, R.N.1
-
11
-
-
0037003049
-
Ex vivo high-resolution magnetic resonance imaging of the brain in Joubert's syndrome
-
Padgett KR, Maria BL, Yachnis AT, Blackband SJ: Ex vivo high-resolution magnetic resonance imaging of the brain in Joubert's syndrome. J Child Neurol 2002;17:911-913.
-
(2002)
J. Child Neurol.
, vol.17
, pp. 911-913
-
-
Padgett, K.R.1
Maria, B.L.2
Yachnis, A.T.3
Blackband, S.J.4
-
12
-
-
0033028321
-
Activation of distinct motor cortex regions during ipsilateral and contralateral finger movements
-
Cramer SC, Finklestein SP, Schaechter JD, et al: Activation of distinct motor cortex regions during ipsilateral and contralateral finger movements. J Neurophysiol 1999;81:383-387.
-
(1999)
J. Neurophysiol.
, vol.81
, pp. 383-387
-
-
Cramer, S.C.1
Finklestein, S.P.2
Schaechter, J.D.3
-
13
-
-
12344294700
-
Assessing the significance of focal activations using their spatial extent
-
Friston KJ, Worsley KJ, Frackowiak RSJ, et al: Assessing the significance of focal activations using their spatial extent. Hum Brain Mapp 1994;1:214-220.
-
(1994)
Hum. Brain Mapp.
, vol.1
, pp. 214-220
-
-
Friston, K.J.1
Worsley, K.J.2
Frackowiak, R.S.J.3
-
14
-
-
0037930794
-
Motor cortex organization after stroke is related to side of stroke and level of recovery
-
Zemke AC, Heagerty PJ, Lee C, Cramer SC: Motor cortex organization after stroke is related to side of stroke and level of recovery. Stroke 2003;34:e23-e28.
-
(2003)
Stroke
, vol.34
-
-
Zemke, A.C.1
Heagerty, P.J.2
Lee, C.3
Cramer, S.C.4
-
16
-
-
0027518327
-
Individual patterns of functional reorganization in the human cerebral cortex after capsular infarction
-
Weiller C, Ramsay SC, Wise RJ, et al: Individual patterns of functional reorganization in the human cerebral cortex after capsular infarction. Ann Neurol 1993;33:181-189.
-
(1993)
Ann. Neurol.
, vol.33
, pp. 181-189
-
-
Weiller, C.1
Ramsay, S.C.2
Wise, R.J.3
-
17
-
-
0031467529
-
A functional MRI study of subjects recovered from hemiparetic stroke
-
Cramer SC, Nelles G, Benson RR, et al: A functional MRI study of subjects recovered from hemiparetic stroke. Stroke 1997;28:2518-2527.
-
(1997)
Stroke
, vol.28
, pp. 2518-2527
-
-
Cramer, S.C.1
Nelles, G.2
Benson, R.R.3
-
18
-
-
0031974190
-
Pilot study of functional MRI to assess cerebral activation of motor function after poststroke hemiparesis
-
Cao Y, D'Olhaberriague L, Vikingstad EM, et al: Pilot study of functional MRI to assess cerebral activation of motor function after poststroke hemiparesis. Stroke 1998;29:112-122.
-
(1998)
Stroke
, vol.29
, pp. 112-122
-
-
Cao, Y.1
D'Olhaberriague, L.2
Vikingstad, E.M.3
-
19
-
-
0037302196
-
Clinical and genetic aspects of the Joubert syndrome: A disorder characterised by cerebellar vermian hypoplasta and accompanying brainstem malformations
-
Bennett CL, Meuleman J, Chance PF, Glass IA: Clinical and genetic aspects of the Joubert syndrome: A disorder characterised by cerebellar vermian hypoplasta and accompanying brainstem malformations. Curr Genom 2003;4:123-129.
-
(2003)
Curr. Genom.
, vol.4
, pp. 123-129
-
-
Bennett, C.L.1
Meuleman, J.2
Chance, P.F.3
Glass, I.A.4
-
20
-
-
0037154038
-
A search for genes involved in Joubert syndrome: Evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8 and BARHL1
-
Blair IP, Gibson RR, Bennett CL, Chance PF: A search for genes involved in Joubert syndrome: Evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8 and BARHL1. Am J Med Genet 2002;107:190-196.
-
(2002)
Am. J. Med. Genet.
, vol.107
, pp. 190-196
-
-
Blair, I.P.1
Gibson, R.R.2
Bennett, C.L.3
Chance, P.F.4
-
21
-
-
0027183543
-
Functional magnetic resonance imaging of motor cortex: Hemispheric asymmetry and handedness
-
Kim S-G, Ashe J, Hendrich K, et al: Functional magnetic resonance imaging of motor cortex: Hemispheric asymmetry and handedness. Science 1993;261:615-617.
-
(1993)
Science
, vol.261
, pp. 615-617
-
-
Kim, S.-G.1
Ashe, J.2
Hendrich, K.3
-
22
-
-
0033571852
-
Gaze direction modulates finger movement activation patterns in human cerebral cortex
-
Baker JT, Donoghue JP, Sanes JN: Gaze direction modulates finger movement activation patterns in human cerebral cortex. J Neurosci 1999;19:10044-10052.
-
(1999)
J. Neurosci.
, vol.19
, pp. 10044-10052
-
-
Baker, J.T.1
Donoghue, J.P.2
Sanes, J.N.3
-
23
-
-
0029992350
-
Cerebral activation covaries with movement rate
-
Schlaug G, Sanes JN, Thangaraj V, et al: Cerebral activation covaries with movement rate. Neuroreport 1996;7:879-883.
-
(1996)
Neuroreport
, vol.7
, pp. 879-883
-
-
Schlaug, G.1
Sanes, J.N.2
Thangaraj, V.3
-
24
-
-
0036109573
-
Holoprosencephaly in children: Diffusion tensor MR imaging of white matter tracts of the brainstem - Initial experience
-
Albayram S, Melhem ER, Mori S, et al: Holoprosencephaly in children: Diffusion tensor MR imaging of white matter tracts of the brainstem - Initial experience. Radiology 2002;223:645-651.
-
(2002)
Radiology
, vol.223
, pp. 645-651
-
-
Albayram, S.1
Melhem, E.R.2
Mori, S.3
|