These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 17355480)

  • 1. Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3).
    Balci S; Unal A; Engiz O; Aktas D; Liehr T; Gross M; Mrasek K; Saygi S
    Dev Med Child Neurol; 2007 Mar; 49(3):219-24. PubMed ID: 17355480
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
    Parrini E; Ramazzotti A; Dobyns WB; Mei D; Moro F; Veggiotti P; Marini C; Brilstra EH; Dalla Bernardina B; Goodwin L; Bodell A; Jones MC; Nangeroni M; Palmeri S; Said E; Sander JW; Striano P; Takahashi Y; Van Maldergem L; Leonardi G; Wright M; Walsh CA; Guerrini R
    Brain; 2006 Jul; 129(Pt 7):1892-906. PubMed ID: 16684786
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Periventricular nodular heterotopia with overlying polymicrogyria.
    Wieck G; Leventer RJ; Squier WM; Jansen A; Andermann E; Dubeau F; Ramazzotti A; Guerrini R; Dobyns WB
    Brain; 2005 Dec; 128(Pt 12):2811-21. PubMed ID: 16311271
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Like father, like son: periventricular nodular heterotopia and nonverbal learning disorder.
    McCann MV; Pongonis SJ; Golomb MR; Edwards-Brown M; Christensen CK; Sokol DK
    J Child Neurol; 2008 Aug; 23(8):950-3. PubMed ID: 18660478
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Bilateral periventricular nodular heterotopia in a couple mother-infant].
    Stival G; Braga M; Di Marco A; Riva E
    Pediatr Med Chir; 2005; 27(1-2):115-8. PubMed ID: 16922057
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Development and developmental disorders of the human brain. III. Neuronal migration disorders of the cerebrum].
    ten Donkelaar HJ; Lammens M; Wesseling P; Thijssen HO; Renier WO; Gabreëls FJ
    Ned Tijdschr Geneeskd; 2001 Mar; 145(10):466-74. PubMed ID: 11268908
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epilepsy and genetic malformations of the cerebral cortex.
    Guerrini R; Carrozzo R
    Am J Med Genet; 2001; 106(2):160-73. PubMed ID: 11579436
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mosaic mutations of the FLN1 gene cause a mild phenotype in patients with periventricular heterotopia.
    Parrini E; Mei D; Wright M; Dorn T; Guerrini R
    Neurogenetics; 2004 Sep; 5(3):191-6. PubMed ID: 15459826
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic malformations of cortical development.
    Guerrini R; Marini C
    Exp Brain Res; 2006 Aug; 173(2):322-33. PubMed ID: 16724181
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation.
    Grosso S; Fichera M; Galesi O; Luciano D; Pucci L; Giardini F; Berardi R; Balestri P
    Dev Med Child Neurol; 2008 Jun; 50(6):473-6. PubMed ID: 18384621
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epilepsy and mental retardation limited to females: an under-recognized disorder.
    Scheffer IE; Turner SJ; Dibbens LM; Bayly MA; Friend K; Hodgson B; Burrows L; Shaw M; Wei C; Ullmann R; Ropers HH; Szepetowski P; Haan E; Mazarib A; Afawi Z; Neufeld MY; Andrews PI; Wallace G; Kivity S; Lev D; Lerman-Sagie T; Derry CP; Korczyn AD; Gecz J; Mulley JC; Berkovic SF
    Brain; 2008 Apr; 131(Pt 4):918-27. PubMed ID: 18234694
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Periventricular nodular and subcortical neuronal heterotopia in adult epileptic patients.
    Consalvo DE; Kochen SS; Alurralde A; Centurion E; Salgado PA; Saidon P; Sica RE
    Medicina (B Aires); 2006; 66(2):101-7. PubMed ID: 16715756
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The recognition and investigation of X-linked learning disability syndromes.
    Feldman EJ
    J Intellect Disabil Res; 1996 Oct; 40 ( Pt 5)():400-11. PubMed ID: 8906528
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An analysis of epilepsy with chromosomal abnormalities.
    Yamanouchi H; Imataka G; Nakagawa E; Nitta A; Suzuki N; Hirao J; Suzumura H; Watanabe H; Arisaka O; Eguchi M
    Brain Dev; 2005 Aug; 27(5):370-7. PubMed ID: 16023555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Paternal inheritance of classic X-linked bilateral periventricular nodular heterotopia.
    Kasper BS; Kurzbuch K; Chang BS; Pauli E; Hamer HM; Winkler J; Hehr U
    Am J Med Genet A; 2013 Jun; 161A(6):1323-8. PubMed ID: 23636902
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopenia.
    Kunishima S; Ito-Yamamura Y; Hayakawa A; Yamamoto T; Saito H
    J Hum Genet; 2010 Dec; 55(12):844-6. PubMed ID: 20844545
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuronal migration disorders, genetics, and epileptogenesis.
    Guerrini R; Filippi T
    J Child Neurol; 2005 Apr; 20(4):287-99. PubMed ID: 15921228
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial neuronal migration disorder: subcortical laminar heterotopia in a mother and pachygyria in the son.
    Toyama J; Kasuya H; Higuchi S; Kondo H; Naganuma Y; Uchiyama M
    Am J Med Genet; 1998 Feb; 75(5):481-4. PubMed ID: 9489790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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. PubMed ID: 7676153
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.