-
3
-
-
0022594340
-
Volumetric development of the fetal telencephalon, cerebral cortex, diencephalon, and rhombencephalon including the cerebellum in man
-
H-J Kretschmann, 2nd end., Bibliotheca Anatomica no 28, Karger, Basel
-
(1986)
Brain growth
, pp. 53-78
-
-
Koop1
Rilling2
Herrmann3
Kretschmann4
-
4
-
-
0017145028
-
Some quantitative morphological aspects of postnatal human cerebellar growth
-
(1976)
J Neurol Sci
, vol.29
, pp. 137-148
-
-
Gadsdon1
Emery2
-
5
-
-
0014835132
-
Histogenesis of cortical layers in human cerebellum, particularly the lamina dissecans
-
(1970)
J Comp Neurol
, vol.139
, pp. 473-500
-
-
Rakic1
Sidman2
-
6
-
-
0018936531
-
Human cerebellar hypoplasia: a syndrome or diverse causes
-
(1980)
Arch Neurol
, vol.37
, pp. 300-305
-
-
Sarnat1
Alcalá2
-
8
-
-
0021331375
-
Defects in specific associations between astroglia and neurons occur in microcultures of weaver mouse cerebellar cells
-
(1984)
J Neurosci
, vol.4
, pp. 1163-1172
-
-
Hatten1
Liem2
Mason3
-
9
-
-
0025239422
-
Riding the glial monorail: a common mechanism for glial-guided neuronal migration in different regions of the developing mammalian brain
-
(1990)
Trends Neurosci
, vol.13
, pp. 179-184
-
-
Hatten1
-
13
-
-
0025341315
-
The cellular basis of segmentation in the developing hindbrain
-
(1990)
Trends Neurosci
, vol.13
, pp. 329-335
-
-
Lumsden1
-
16
-
-
0026544277
-
Lethal cytomegalovirus infection in preterm infants: clinical, radiological, and neuropathological findings
-
(1992)
Ann Neurol
, vol.31
, pp. 64-68
-
-
Perlman1
Argyle2
-
19
-
-
0001676883
-
Primary degeneration of the granular layer of the cerebellum: an unusual form of familial cerebellar atrophy occurring in early life
-
(1940)
Brain
, vol.63
, pp. 365-379
-
-
Norman1
-
27
-
-
0027516363
-
Infantile cerebello-optic atrophy: neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome)
-
(1993)
Acta Neuropathol
, vol.85
, pp. 241-247
-
-
Haltia1
Somer2
-
30
-
-
0021645906
-
An infantile autistic syndrome characterised by the presence of succinylpurines in body fluids
-
(1984)
Lancet
, vol.2
, pp. 1058-1061
-
-
Jaeken1
van den Berghe2
-
37
-
-
0026471582
-
Autosomal recessive oralfacial-digital syndrome with resemblance to OFD types II, III, IV and VI: a new OFD syndrome?
-
(1992)
Am J Med Genet
, vol.44
, pp. 567-572
-
-
Chitayat1
Stalker2
Azouz3
-
38
-
-
0020076144
-
Olivopontocerebellar atrophy: a review of 117 cases
-
(1982)
J Neurol Sci
, vol.53
, pp. 253-272
-
-
Berciano1
-
42
-
-
15444343578
-
Zur Kenntnis der Bildungsfehler des Kleinhirns. Epikritische Bemerkungen zur Entwicklungspathologie, Morphologie und Klinik der umschriebenen Entwicklungshemmungen des Neozerebellums
-
(1917)
Schweiz Arch Neurol Psychiatr
, vol.1
, pp. 48-105
-
-
Brun1
-
50
-
-
0002513078
-
Cerebellar hypoplasia in Werdnig-Hoffmann disease
-
(1961)
Arch Dis Child
, vol.36
, pp. 96-101
-
-
Norman1
-
57
-
-
0023122838
-
Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset
-
(1987)
Virchows Arch A
, vol.410
, pp. 339-345
-
-
Moerman1
Barth2
-
58
-
-
0002239501
-
Inherited disorders of the fetal brain: a field in need of recognition
-
Y Fukuyama, Y Suzuki, S Kamoshita, P Casaer, Karger, Basel
-
(1992)
Fetal and perinatal neurology
, pp. 299-313
-
-
Barth1
-
59
-
-
0021147521
-
Pontoneocerebellar hypoplasia: a probable consequence of prenatal destruction of the pontine nuclei and a possible role of phenytoin intoxication
-
(1984)
Clin Neuropathol
, vol.3
, pp. 160-167
-
-
Gadisseux1
Rodriguez2
Lyon3
-
60
-
-
0022787575
-
Neocerebellar hypoplasia with systemic combined olivo-ponto-dentatal degeneration in a 9-day-old baby: contribution to the problem of relations between malformation and systemic degeneration in early life
-
(1986)
Clin Neuropathol
, vol.5
, pp. 203-208
-
-
Kawagoe1
Jacob2
-
63
-
-
0017325923
-
Congenital spongy degeneration of the brain (Van Bogaert-Bertrand) associated with micrencephaly and ponto-cerebellar atrophy (contributions to the pathology of glial dystrophy of intrauterine origin)
-
(1977)
Neuropädiatrie
, vol.8
, pp. 73-87
-
-
Vuia1
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