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References
- Embryology of the craniocervical junction and posterior cranial fossa, part II: embryogenesis of the hindbrain.Clin Anat. 2018; 31: 488-500
- Basic genetic principles applied to posterior fossa malformations.Top Magn Reson Imaging. 2011; 22: 261-270
- The fetal posterior fossa on prenatal ultrasound imaging: normal longitudinal development and posterior fossa anomalies.Eur J Ultrasound. 2019; 40: 692-721
- Congenital basis of posterior fossa anomalies.Neuroradiology J. 2015; 28: 238-253
- Posterior fossa malformations.Semin Ultrasound CT MR. 2011; 32: 228-241
- Assessment of fetal midbrain and hindbrain in mid-sagittal cranial plane by three-dimensional multiplanar sonography. part 1: comparison of new and established nomograms.Ultrasound Obstet Gynecol. 2014; 44: 575-580
- Diagnostic imaging of posterior fossa anomalies in the fetus and neonate: Part 1, normal anatomy and classification of anomalies.Clin Imaging. 2015; 39: 1-8
- Congenital abnormalities of the posterior fossa.RadioGraphics. 2015; 35: 200-220
- Prenatal imaging of posterior fossa disorders. a review.Eur J Paediatric Neurol. 2018; 22: 972-988
- A developmental and genetic classification for midbrain-hindbrain malformations.Brain. 2009; 132: 3199-3230
- Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics.Lancet Neurol. 2013; 12: 381-393
- Pre- and postnatal neuroimaging of congenital cerebellar abnormalities.Cerebellum. 2015; 15: 5-9
- Multiple developmental programs are altered by loss of zic1 and ZIC4 to cause Dandy-Walker malformation cerebellar pathogenesis.Development. 2011; 138: 1207-1216
- Ultrasound and CT of the posterior fossa in neonates.From Embryology to Diagnostic Investigations, Cerebellum2018: 205-217
- Hydrocephalus in Dandy-Walker malformation.Childs Nerv Syst. 2011; 27 (Epub 2011 Sep 17): 1665-1681
- Stereotactic endoscopic interventions in cystic brain lesions.Adv Stereotactic Funct Neurosurg. 1995; 11: 59-63
- Intracranial arachnoid cyst family with autosomal recessive trait mapped to chromosome 6q22.31-23.2.Acta Neurochir. 2012; 154: 1287-1292
- Diagnostic imaging of posterior fossa anomalies in the fetus.Semin Fetal Neonatal Med. 2016; 21: 312-320
- Congenital malformations of the posterior cranial fossa.Rivista Di Neuroradiologia. 2000; 13: 41-44
- Blake's pouch cyst: an entity within the Dandy-Walker Continuum.Neuroradiology. 2000; 42: 290-295
- Macrocerebellum: significance and pathogenic considerations.Cerebellum. 2012; 11: 1026-1036
- Rhombencephalosynapsis: fused cerebellum, confused geneticists.Am J Med Genet C: Semin Med Genet. 2018; 178: 432-439
- Partial rhombencephalosynapsis.Am J Neuroradiol. 2004; 25: 29-31
- Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity.Brain. 2012; 135: 1370-1386
- Transformation of the cerebellum into more ventral brainstem fates causes cerebellar agenesis in the absence of ptf1a function.Proc Natl Acad Sci. 2014; 111: E1777-E1786
- Magnetic resonance imaging of malformations of midbrain-hindbrain.J Computer Assisted Tomography. 2016; 40: 14-25
- Neuronal migration disorders.Neurobiol Dis. 2010; 38: 154-166
- Mutations in VLDLR as a cause for autosomal recessive cerebellar ataxia with mental retardation (DYSEQUILIBRIUM syndrome).J Child Neurol. 2009; 24: 1310-1315
- Cerebellar hypoplasia: Differential diagnosis and diagnostic approach.Am J Med Genet C: Semin Med Genet. 2014; 166: 211-226
- Cerebellar cleft: confirmation of the neuroimaging pattern.Neuropediatrics. 2009; 40: 228-233
- Cerebellar dysplasia.in: Boltshauser E. Schmahmann J.D. Cerebellar disorders in children. Mac Keith, London, England2012: 172-176
- Abnormalities of cerebellar foliation and fissuration: classification, neurogenetics and clinicoradiological correlations.Neuroradiology. 2002; 44: 639-646
- Louis vallee, and jean pierre pruvo cerebellar cortical dysplasia: MR findings in a complex entity.AJNR Am J Neuroradiol. 2000; 21: 1511-1519
- Cerebellum of the premature infant: rapidly developing, vulnerable, clinically important.J Child Neurol. 2009; 24: 1085-1104
- Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients.Neuropediatrics. 2011; 42https://doi.org/10.1055/s-0031-1274082
- Joubert syndrome: Insights into Brain Development, cilium biology, and complex disease.Semin Pediatr Neurol. 2009; 16: 143-154
- Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasia.Orphanet J Rare Dis. 2011; 6: 50
- CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.Cell. 2014; 157: 651-663
- Brain involvement in muscular dystrophies with defective dystroglycan glycosylation.Ann Neurol. 2008; 64: 573-582
- Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies.Brain. 2012; 135 (Epub 2012 Feb 9): 469-482
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Published online: August 19, 2022
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