Dizygotic Twins with Schizencephaly and Focal Cortical Dysplasia

References

1. ↵
   Barkovich AJ, Kjos BO. Schizencephaly: correlation of clinical findings with MR characteristics. AJNR Am J Neuroradiol 1992;13:85-94

   Abstract/FREE Full Text
2. ↵
   Komarniski CA, Cyr DR, Mack LA, Weinberger E. Prenatal diagnosis of schizencephaly. J Ultrasound Med 1990;9:305-307

   PubMed
3. ↵
   Ueda M, Kamiya T, Ohyama M, Katayama Y, Terashi A. Two siblings with familial schizencephaly: report of a family and review in relation to clinical features and neuroradiological findings [in Japanese]. Rinsho Shinkeigaku 1996;36:774-779

   PubMed
4. Haverkamp F, Zerres K, Ostertun B, Emons D, Lentze MJ. Familial schizencephaly: further delineation of a rare disorder. J Med Genet 1995;32:242-244

   Abstract/FREE Full Text
5. Hosley MA, Abroms IF, Ragland RL. Schizencephaly: case report of familial incidence. Pediatr Neurol 1992;8:148-150

   CrossRefPubMedWeb of Science
6. ↵
   Packard AM, Miller VS, Delgado MR. Schizencephaly: correlations of clinical and radiologic features. Neurology 1997;48:1427-1434

   Abstract/FREE Full Text
7. Iannetti P, Nigro G, Spalice A, Faiella A, Boncinelli E. Cytomegalovirus infection and schizencephaly: case reports. Ann Neurol 1998;43:123-127

   CrossRefPubMedWeb of Science
8. Granata T, Farina L, Faiella A, et al. Familial schizencephaly associated with EMX2 mutation. Neurology 1997;48:1403-1406

   Abstract/FREE Full Text
9. ↵
   Barkovich AJ, Norman D. Absence of the septum pellucidum: a useful sign in the diagnosis of congenital brain malformations. AJR Am J Roentgenol 1989;152:353-360

   PubMedWeb of Science
10. Barkovich AJ. Congenital malformations of the brain and skull. In: Barkovich AJ, ed. Pediatric Neuroimaging. 2nd ed. New York: Raven; 1995: 219-225
11. Sarwar M. The septum pellucidum: normal and abnormal. AJNR Am J Neuroradiol 1989;10:989-1005

    Abstract/FREE Full Text