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Morphological neuroimaging of malformations of cortical development Volume 5, numéro 2, June 2003

1. Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. Classification system for malformation of cortical development: update 2001. Neurology 2001; 57: 2168-78.

2. Barkovich AJ, Ferrero DM, Barr RM, et al. Microlissencephaly, a heterogeneous malformation of cortical development. Neuropediatrics 1998; 29: 113-9.

3. Harris RM, Carter NP, Griffiths B, et al. Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34. Genomics 1993; 15: 265-74.

4. Consortium ECTS. Identification and characterization of the tuberous sclerosis gene on chromosome 16. Cell 1993; 75: 1305-15.

5. Kingsley D, Kendall B, Fitz C. Tuberous sclerosis: a clinico-radiological evaluation of 110 cases with particular reference to atypical presentation. Neuroradiology 1986; 28: 171-90.

6. Christophe C, Bartholome J, Blum D, et al. Neonatal tuberous sclerosis. US, CT, and MR diagnosis of brain and cardiac lesions. Pediatr Radiol 1989; 19 (6-7): 446-8.

7. Gomez M. Tuberous sclerosis. 2nd ed. New York: Raven Press, 1988.

8. Braffmann B, Bilaniuk L, Naidich T, et al. MR imaging of tuberous sclerosis: pathogenesis of this phakomatosis, use of gadopentate dimeglumine, and literature review. Radiology 1992; 183: 227-38.

9. Barkovich AJ, Gressens P, Evrard P. Formation, maturation and disorders of brain neocortex. Am J Neuroradiol 1992; 13: 423-46.

10. Barkovich AJ, Kuzniecky RI, Bollen AW, Grant PE. Focal transmantle dysplasia: a specific malformation of cortical development. Neurology 1997; 49: 1148-52.

11. Palmini A, Andermann F, Olivier A, Tampieri D, Robitaille Y. Focal neuronal migration, disorders and intractable partial epilepsy: result of surgical treatment. Ann Neurol 1991; 30: 750-7.

12. Barkovich AJ. Pediatric Neuroimaging. 3rd ed. Philadelphia: Lippincott Williams and Wilkins, 2000.

13. Barkovich AJ, Chuang SH. Unilateral megalencephaly: correlation of MR imaging and pathologic characteristics. Am J Neuroradiol 1990; 11: 523-31.

14. Paione L, Curatolo P, Rizzo R, et al. Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures and facial hemiatrophy. Neurology 1991; 41: 266-71.

15. Griffiths PD, Welch R, Gardner-Medwin D, et al. The radiological features of hemimegalencephaly including three cases associated with proteus syndrome. Neuropediatrics 1994; 25: 140-4.

16. Peserico A, Battistella PA, Bertoli P, et al. Unilateral hypomelanosis of Ito with megalencephaly. Acta Paediatr Scand 1988; 77: 446-7.

17. Wolpert SM, Cohen A, Libenson M. Hemimegalencephaly: a longitudinal MR study. Am J Neuroradiol 1994; 15: 1479-82.

18. Villemure JG. Hemispherectomy techniques. A critical review. In: Tuxhorn I, Holthausen H, Boenigk H eds. Paediatric epilepsy syndromes and their surgical treatment. London: John Libbey, 1997: 729-38.

19. Tampieri D, Moundjian H, Melanson D, Ethier R. Intracerebral gangliogliomas in patients with partial complex seizures: CT and MR imaging findings. Am J Neuroradiol 1991; 12: 749-55.

20. Lipper MH, Eberhard DA. Pleomorphic xanthoastrocytoma, a distinctive astroglial tumor: neuroradiologic and pathologic features. Am J Neuroradiol 1993; 141: 1397-404.

21. Stanescu Cosson R, Varlet P, Beuvon F, et al. Dysembryoplastic neuroepithelial tumors: CT, MR findings and imaging follow-up: a study of 53 cases. J Neuroradiol 2001 ; 28: 230-40.

22. Dobyns WB, Truwit CL. Lissencephaly and other malformations of cortical development. Neuropediatrics 1995; 26: 132-47.

23. Dobyns WB, Truwit CL, Ross ME, et al. Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly. Neurology 1999; 53: 270-7.

24. Raybaud C, Girard N, Canto-Moreira F, et al. High-definition magnetic resonance imaging of cortical dysplasias: micropolygyria versus lissencephaly. In: Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin BG, Pfaner P, eds. Dysplasias of cerebral cortex and epilepsy. Philadelphia: Lippincott-Raven Publisher, 1996: 131-43.

25. Rosa ME, Swanson K, Dobyns WB. Lissencephaly with cerebellar hypoplasia (LCH). A heterogeneous group of cortical malformations. Neuropediatrics 2001; 32: 256-63.

26. Barkovich AJ. Neuroimaging manifestations and classification of congenital muscular dystrophies. Am J Neuroradiol 1998; 19: 1389-96.

27. Pilz D, Stoodley N, Jeffrey A, Golden J. Neuronal migration, cerebral cortical development and cerebral cortical anomalies. J Neuropathol Exp Neurol 2002; 61: 1-11.

28. Squier MV. Development of the cortical dysplasia of type II lissencephaly. Neuropathol Appl Neurobiol 1993; 19: 209-13.

29. Barkovich AJ. Morphological characteristics of subcortical heterotopia: MR imaging study. Am J Neuroradiol 2000; 21: 290-5.

30. Eksioglu YZ, Scheffer IE, Cardenas P, et al. Periventricular heterotopia: an X-linked dominant epilepsy causing aberrant cerebral cortical development. Neuron 1996; 16: 77-87.

31. Dobyns WB, Guerrini R, Czapans H, Beilman D. Bilateral periventricular nodular heterotopia with mental retardation and with syndactily in boys: a new X-linked mental retardation syndrome. Neurology 1997; 49: 1042-7.

32. Barkovich AJ, Guerrini R, Battaglia G, et al. Band heterotopia: correlation of outcome with MR imaging parameters. Ann Neurol 1994; 36: 609-17.

33. Gleeson JG, Allen KA, Fox JW, et al. Double cortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 1998; 92: 63-72.

34. Barkovich AJ, Rowley HA, Bollen A. Correlation of prenatal events with the development of polymicrogyria. Am J Neuroradiol 1995; 16: 822-7.

35. Kuzniecky R, Andermann F, Guerrini R. Congenital bilateral perisylvian syndrome: study of 31 patients. The congenital bilateral perisylvian syndrome multicenter collaborative study. Lancet 1993; 341: 608-12.

36. Yakovlev PI, Wadsworth RC. Schizencephalies. A study of the congenital clefts in the cerebral mantle. 1. Clefts with fused lips. J Neuropathol Exp Neurol 1946; 5: 116-30.

37. Yakovlev PI, Wadsworth RC. Schizencephalies. A study of the congenital clefts in the cerebral mantle. 2. Clefts with hydrocephalus and lips separated. J Neuropathol Exp Neurol 1946; 5: 169-206.

38. Barkovich AJ, Hevner R, Guerrini R. Syndromes of bilateral symmetrical polymicrogyria. Am J Neuroradiol 1999; 20: 1814-21.

39. Barkovich AJ, Kjos BO. Schizencephaly, correlation of clinical findings with MR characteristics. Am J Neuroradiol 1992; 13: 85-94.

40. Barkovich AJ, Fram EK, Norman D. Septo-optic dysplasia: MR imaging. Radiology 1989; 171: 189-92.

41. Brunelli S, Faiella A, Capra V, et al. Germline mutations in the homeobox gene EMX 2 in patients with severe schizencephaly. Nat Genet 1996; 12: 94-6.

42. Granata T, Farina L, Faiella A, et al. Familial schizencephaly associated with EMX2 mutation. Neurology 1997; 48: 1403-6.