121 related articles for article (PubMed ID: 14617419)
1. Etiological classification of CNS malformations: integration of molecular genetic and morphological criteria.
Sarnat HB; Flores-Sarnat L
Epileptic Disord; 2003 Sep; 5 Suppl 2():S35-43. PubMed ID: 14617419
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic and morphologic integration in malformations of the nervous system for etiologic classification.
Sarnat HB; Flores-Sarnat L
Semin Pediatr Neurol; 2002 Dec; 9(4):335-44. PubMed ID: 12523557
[TBL] [Abstract][Full Text] [Related]
3. [A proposal for a molecular genetic classification of the malformations of the nervous system].
Sarnat HB
Rev Neurol; 2001 Jul 1-15; 33(1):68-75. PubMed ID: 11562863
[TBL] [Abstract][Full Text] [Related]
4. Integrative classification of morphology and molecular genetics in central nervous system malformations.
Sarnat HB; Flores-Sarnat L
Am J Med Genet A; 2004 May; 126A(4):386-92. PubMed ID: 15098236
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetic classification of central nervous system malformations.
Sarnat HB
J Child Neurol; 2000 Oct; 15(10):675-87. PubMed ID: 11063082
[TBL] [Abstract][Full Text] [Related]
6. Current concepts of the etiology of central nervous system malformations.
Melnick M
Birth Defects Orig Artic Ser; 1979; 15(3):19-41. PubMed ID: 380680
[TBL] [Abstract][Full Text] [Related]
7. A developmental and genetic classification for malformations of cortical development.
Barkovich AJ; Kuzniecky RI; Jackson GD; Guerrini R; Dobyns WB
Neurology; 2005 Dec; 65(12):1873-87. PubMed ID: 16192428
[TBL] [Abstract][Full Text] [Related]
8. Malformations of cortical development and epilepsy, part 1: diagnosis and classification scheme.
Kuzniecky RI
Rev Neurol Dis; 2006; 3(4):151-62. PubMed ID: 17224898
[TBL] [Abstract][Full Text] [Related]
9. Location and type of mutation in the LIS1 gene do not predict phenotypic severity.
Uyanik G; Morris-Rosendahl DJ; Stiegler J; Klapecki J; Gross C; Berman Y; Martin P; Dey L; Spranger S; Korenke GC; Schreyer I; Hertzberg C; Neumann TE; Burkart P; Spaich C; Meng M; Holthausen H; Adès L; Seidel J; Mangold E; Buyse G; Meinecke P; Schara U; Zeschnigk C; Muller D; Helland G; Schulze B; Wright ML; Kortge-Jung S; Hehr A; Bogdahn U; Schuierer G; Kohlhase J; Aigner L; Wolff G; Hehr U; Winkler J
Neurology; 2007 Jul; 69(5):442-7. PubMed ID: 17664403
[TBL] [Abstract][Full Text] [Related]
10. Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).
Poirier K; Keays DA; Francis F; Saillour Y; Bahi N; Manouvrier S; Fallet-Bianco C; Pasquier L; Toutain A; Tuy FP; Bienvenu T; Joriot S; Odent S; Ville D; Desguerre I; Goldenberg A; Moutard ML; Fryns JP; van Esch H; Harvey RJ; Siebold C; Flint J; Beldjord C; Chelly J
Hum Mutat; 2007 Nov; 28(11):1055-64. PubMed ID: 17584854
[TBL] [Abstract][Full Text] [Related]
11. Genetic assessment of cortical malformations.
Hehr U; Schuierer G
Neuropediatrics; 2011 Feb; 42(2):43-50. PubMed ID: 21692014
[TBL] [Abstract][Full Text] [Related]
12. Neuropathologic research strategies in holoprosencephaly.
Sarnat HB; Flores-Sarnat L
J Child Neurol; 2001 Dec; 16(12):918-31. PubMed ID: 11785508
[TBL] [Abstract][Full Text] [Related]
13. Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.
Morris-Rosendahl DJ; Najm J; Lachmeijer AM; Sztriha L; Martins M; Kuechler A; Haug V; Zeschnigk C; Martin P; Santos M; Vasconcelos C; Omran H; Kraus U; Van der Knaap MS; Schuierer G; Kutsche K; Uyanik G
Clin Genet; 2008 Nov; 74(5):425-33. PubMed ID: 18954413
[TBL] [Abstract][Full Text] [Related]
14. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
Stalmans I
Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
[TBL] [Abstract][Full Text] [Related]
15. Morphological neuroimaging of malformations of cortical development.
D'Incerti L
Epileptic Disord; 2003 Sep; 5 Suppl 2():S59-66. PubMed ID: 14617422
[TBL] [Abstract][Full Text] [Related]
16. Magnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene.
Tijssen MA; Brown P; MacManus D; McLean MA; Davie C
Mov Disord; 2003 Dec; 18(12):1538-41. PubMed ID: 14673895
[TBL] [Abstract][Full Text] [Related]
17. Genetic advances in central nervous system malformations in the fetus and neonate.
Jeng LB; Tarvin R; Robin NH
Semin Pediatr Neurol; 2001 Jun; 8(2):89-99. PubMed ID: 11464961
[TBL] [Abstract][Full Text] [Related]
18. Risk of recurrence in major central nervous system malformations between 1976 and 2005.
Joó JG; Beke A; Papp Z; Csaba A; Rab A; Papp C
Prenat Diagn; 2007 Nov; 27(11):1028-32. PubMed ID: 17694579
[TBL] [Abstract][Full Text] [Related]
19. Haploinsufficiency of the murine polycomb gene Suz12 results in diverse malformations of the brain and neural tube.
Miró X; Zhou X; Boretius S; Michaelis T; Kubisch C; Alvarez-Bolado G; Gruss P
Dis Model Mech; 2009; 2(7-8):412-8. PubMed ID: 19535498
[TBL] [Abstract][Full Text] [Related]
20. Genetic malformations of the cerebral cortex and epilepsy.
Guerrini R
Epilepsia; 2005; 46 Suppl 1():32-7. PubMed ID: 15816977
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
