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Items: 1 to 20 of 28

1.

Males with epilepsy, complete subcortical band heterotopia, and somatic mosaicism for DCX.

Poolos NP, Das S, Clark GD, Lardizabal D, Noebels JL, Wyllie E, Dobyns WB.

Neurology. 2002 May 28;58(10):1559-62.

PMID:
12034802
2.

[Subcortical band heterotopia].

Takeuchi Y.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):133-6. Review. Japanese. No abstract available.

PMID:
12483846
3.

Epilepsy and genetic malformations of the cerebral cortex.

Guerrini R, Carrozzo R.

Am J Med Genet. 2001 Summer;106(2):160-73. Review.

PMID:
11579436
4.
5.

Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.

Guerrini R, Carrozzo R.

Seizure. 2002 Apr;11 Suppl A:532-43; quiz 544-7. Review.

PMID:
12185771
6.

Genetic malformations of the cerebral cortex and epilepsy.

Guerrini R.

Epilepsia. 2005;46 Suppl 1:32-7. Review.

7.

[Subcortical laminal heterotopia and lissencephaly: cerebral malformations of X-linked inheritance].

Pinard JM, Desguerre I, Motte J, Dulac O, Ponsot G.

Rev Neurol (Paris). 1995 Mar;151(3):171-6. Review. French.

PMID:
7676153
8.

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.

Leventer RJ, Pilz DT, Matsumoto N, Ledbetter DH, Dobyns WB.

Mol Med Today. 2000 Jul;6(7):277-84. Review.

PMID:
10859564
9.

[Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].

Bahi-Buisson N, Boddaert N, Saillour Y, Souville I, Poirier K, Léger PL, Castelnau L, Plouin P, Carion N, Beldjord C, Chelly J.

Rev Neurol (Paris). 2008 Dec;164(12):995-1009. doi: 10.1016/j.neurol.2008.04.006. Epub 2008 Jun 9. Review. French.

PMID:
18808783
10.

X-linked malformations of neuronal migration.

Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O, Guerrini R, Hirsch B, Ledbetter DH, Lee NS, Motte J, Pinard JM, Radtke RA, Ross ME, Tampieri D, Walsh CA, Truwit CL.

Neurology. 1996 Aug;47(2):331-9. Review.

PMID:
8757001
11.

Neuronal migration disorders, genetics, and epileptogenesis.

Guerrini R, Filippi T.

J Child Neurol. 2005 Apr;20(4):287-99. Review.

PMID:
15921228
12.
13.

Diffuse malformations of cortical development.

Bahi-Buisson N, Guerrini R.

Handb Clin Neurol. 2013;111:653-65. doi: 10.1016/B978-0-444-52891-9.00068-3. Review.

PMID:
23622213
14.

[Genetic and clinical aspects of lissencephaly].

Verloes A, Elmaleh M, Gonzales M, Laquerrière A, Gressens P.

Rev Neurol (Paris). 2007 May;163(5):533-47. Review. French.

PMID:
17571022
15.
16.

The possible pathological importance of dysgenesis, heterotopia and other cellular displacements in the brain.

Mouritzen-Dam A.

Epilepsy Res Suppl. 1992;9:61-5. Review. No abstract available.

PMID:
1285915
17.
18.

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.

Dobyns WB, Berry-Kravis E, Havernick NJ, Holden KR, Viskochil D.

Am J Med Genet. 1999 Oct 8;86(4):331-7. Review.

PMID:
10494089
19.

Missense mutations resulting in type 1 lissencephaly.

Reiner O, Coquelle FM.

Cell Mol Life Sci. 2005 Feb;62(4):425-34. Review.

PMID:
15719169
20.

Epilepsy and malformations of the cerebral cortex.

Guerrini R, Sicca F, Parmeggiani L.

Epileptic Disord. 2003 Sep;5 Suppl 2:S9-26. Review.

PMID:
14617417

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