-
1
-
-
0027771377
-
Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset
-
Barth PG (1993) Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset. Brain Dev 15:411-422
-
(1993)
Brain Dev
, vol.15
, pp. 411-422
-
-
Barth, P.G.1
-
2
-
-
34848902266
-
Pontocerebellar hypoplasia type 2: A neuropathological update
-
doi: 10.1007/s00401-007-0263-0
-
Barth PG, Aronica E, de Vries L, Nikkels PGJ, Scheper W, Hoozemans JJ, Poll-The B-T, Troost D (2007) Pontocerebellar hypoplasia type 2: A neuropathological update. Acta Neuropathol. doi: 10.1007/ s00401-007-0263-0
-
(2007)
Acta Neuropathol
-
-
Barth, P.G.1
Aronica, E.2
de Vries, L.3
Nikkels, P.G.J.4
Scheper, W.5
Hoozemans, J.J.6
Poll-The, B.-T.7
Troost, D.8
-
3
-
-
33750984197
-
Olivopontocerebellar atrophy: Toward a better nosological definition
-
Berciano J, Boesch S, Pérez-Ramos JM, Wenning GK (2006) Olivopontocerebellar atrophy: Toward a better nosological definition. Mov Disord 21:1607-1613
-
(2006)
Mov Disord
, vol.21
, pp. 1607-1613
-
-
Berciano, J.1
Boesch, S.2
Pérez-Ramos, J.M.3
Wenning, G.K.4
-
4
-
-
34848872189
-
Congenital pontocerebellar atrophy and telencephalic defects in three siblings: A new subtype
-
doi: 10.1007/s00401-007-0248-z
-
Leroy JG, Lyon G, Fallet C, Amiel J, De Praeter C, Van Den Broecke C, Vanhaesebrouck P (2007) Congenital pontocerebellar atrophy and telencephalic defects in three siblings: A new subtype. Acta Neuropathol doi: 10.1007/s00401-007-0248-z
-
(2007)
Acta Neuropathol
-
-
Leroy, J.G.1
Lyon, G.2
Fallet, C.3
Amiel, J.4
De Praeter, C.5
Van Den Broecke, C.6
Vanhaesebrouck, P.7
-
6
-
-
0004042407
-
-
Oxford University Press, New York
-
Norman MG, McGillivray BC, Kalousek DK, Hill A, Poskitt KJ (1995) Congenital malformations of the brain. Oxford University Press, New York
-
(1995)
Congenital Malformations of the Brain
-
-
Norman, M.G.1
McGillivray, B.C.2
Kalousek, D.K.3
Hill, A.4
Poskitt, K.J.5
-
7
-
-
33749676438
-
Pathology and genetics of multiple system atrophy: An approach to determining genetic susceptibility spectrum
-
Ozawa T (2006) Pathology and genetics of multiple system atrophy: An approach to determining genetic susceptibility spectrum. Acta Neuropathol 112:531-538
-
(2006)
Acta Neuropathol
, vol.112
, pp. 531-538
-
-
Ozawa, T.1
-
8
-
-
33644861122
-
Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5?
-
Patel MS, Becker LE, Toi A, Armstrong DA, Chitayat D (2006) Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5? Am J Med Genet 140A:594-603
-
(2006)
Am J Med Genet
, vol.140 A
, pp. 594-603
-
-
Patel, M.S.1
Becker, L.E.2
Toi, A.3
Armstrong, D.A.4
Chitayat, D.5
-
9
-
-
0038137184
-
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21
-
Rajab A, Mochida GH, Hill A, Ganesh V, Bodell A, Riaz A, Grant PE, Shugart YY, Walsh CA (2003) A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Neurology 60:1664-1667
-
(2003)
Neurology
, vol.60
, pp. 1664-1667
-
-
Rajab, A.1
Mochida, G.H.2
Hill, A.3
Ganesh, V.4
Bodell, A.5
Riaz, A.6
Grant, P.E.7
Shugart, Y.Y.8
Walsh, C.A.9
-
10
-
-
0141627447
-
Development and developmental disorders of the human cerebellum
-
ten Donkelaar HJ, Lammens M, Wesseling P, Thijssen HOM, Reiner WO (2003) Development and developmental disorders of the human cerebellum. J Neurol 250:1025-1036
-
(2003)
J Neurol
, vol.250
, pp. 1025-1036
-
-
ten Donkelaar, H.J.1
Lammens, M.2
Wesseling, P.3
Thijssen, H.O.M.4
Reiner, W.O.5
-
11
-
-
0035253120
-
The rhombic lip and early cerebellar development
-
Wingate RJ (2001) The rhombic lip and early cerebellar development. Curr Opin Neurobiol 11:82-88
-
(2001)
Curr Opin Neurobiol
, vol.11
, pp. 82-88
-
-
Wingate, R.J.1
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