메뉴 건너뛰기




Volumn 15, Issue 6, 1993, Pages 411-422

Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset

Author keywords

Cerebellar hypoplasia; Cerebellum; Neurodegenerative disorder; Olivopontocerebellar atrophy; Pontocerebellar hypoplasia

Indexed keywords

CEREBELLUM HYPOPLASIA; CHOREA; CLINICAL FEATURE; CONTRACTURE; DYSTONIA; FETUS; HUMAN; MICROCEPHALY; MOTOR NEUROPATHY; NERVE DEGENERATION; NEUROPATHOLOGY; NEWBORN; ONSET AGE; PONS ANGLE; RESPIRATORY FAILURE; REVIEW; SPINAL CORD ATROPHY; SPINAL CORD VENTRAL HORN;

EID: 0027771377     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/0387-7604(93)90080-R     Document Type: Article
Times cited : (222)

References (67)
  • 3
    • 0022594340 scopus 로고
    • 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 scopus 로고
    • Some quantitative morphological aspects of postnatal human cerebellar growth
    • (1976) J Neurol Sci , vol.29 , pp. 137-148
    • Gadsdon1    Emery2
  • 5
    • 0014835132 scopus 로고
    • Histogenesis of cortical layers in human cerebellum, particularly the lamina dissecans
    • (1970) J Comp Neurol , vol.139 , pp. 473-500
    • Rakic1    Sidman2
  • 6
  • 8
    • 0021331375 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • The cellular basis of segmentation in the developing hindbrain
    • (1990) Trends Neurosci , vol.13 , pp. 329-335
    • Lumsden1
  • 16
    • 0026544277 scopus 로고
    • Lethal cytomegalovirus infection in preterm infants: clinical, radiological, and neuropathological findings
    • (1992) Ann Neurol , vol.31 , pp. 64-68
    • Perlman1    Argyle2
  • 19
    • 0001676883 scopus 로고
    • 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
  • 26
    • 0021714694 scopus 로고
    • Cerebral calcifications and cerebellar hypoplasia in two children: clinical, radiologic and neuropathological studies — A separate neurodevelopmental entity
    • (1984) Neuropediatrics , vol.15 , pp. 102-109
    • Troost1    van Rossum2    Veiga Pires3    Willemse4
  • 27
    • 0027516363 scopus 로고
    • 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 scopus 로고
    • An infantile autistic syndrome characterised by the presence of succinylpurines in body fluids
    • (1984) Lancet , vol.2 , pp. 1058-1061
    • Jaeken1    van den Berghe2
  • 36
    • 0026062885 scopus 로고
    • Oto-palatal-digital syndrome type II with X-linked cerebellar hypoplasia/hydrocephalus
    • (1991) Am J Med Genet , vol.41 , pp. 169-172
    • Stratton1    Bluestone2
  • 37
    • 0026471582 scopus 로고
    • 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 scopus 로고
    • Olivopontocerebellar atrophy: a review of 117 cases
    • (1982) J Neurol Sci , vol.53 , pp. 253-272
    • Berciano1
  • 42
    • 15444343578 scopus 로고
    • 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
  • 48
    • 0013640686 scopus 로고
    • Hereditäres, der OPCA (olivo-ponto-zerebellaren Atrophie)ähnliches Syndrom bei zwei Geschwisterkindern
    • F Hanefeld, D Rating, H-J Christen, Springer, Berlin, 1989
    • (1990) Aktuelle Neuropädiatrie , pp. 78-80
    • Richardt1    Gullotta2    Hanefeld3
  • 50
    • 0002513078 scopus 로고
    • Cerebellar hypoplasia in Werdnig-Hoffmann disease
    • (1961) Arch Dis Child , vol.36 , pp. 96-101
    • Norman1
  • 56
    • 0018948433 scopus 로고
    • Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease
    • (1980) Ann Neurol , vol.8 , pp. 317-324
    • Steiman1    Rorke2    Brown3
  • 57
    • 0023122838 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.