BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 12682315)

  • 61. Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism?
    Mitchell LA; Thomas PQ; Zacharin MR; Scheffer IE
    AJNR Am J Neuroradiol; 2002 Oct; 23(9):1475-81. PubMed ID: 12372734
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Multiple pterygium syndrome, bilateral periventricular nodular heterotopia and epileptic seizures--a syndrome?
    Holtmann M; Woermann FG; Boenigk HE
    Neuropediatrics; 2001 Oct; 32(5):264-6. PubMed ID: 11748498
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Hereditary nodular heterotopia accompanied by mega cisterna magna.
    Oda T; Nagai Y; Fujimoto S; Sobajima H; Kobayashi M; Togari H; Wada Y
    Am J Med Genet; 1993 Aug; 47(2):268-71. PubMed ID: 8213918
    [TBL] [Abstract][Full Text] [Related]  

  • 64. 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]  

  • 65. Seizure onset from periventricular nodular heterotopias: depth-electrode study.
    Kothare SV; VanLandingham K; Armon C; Luther JS; Friedman A; Radtke RA
    Neurology; 1998 Dec; 51(6):1723-7. PubMed ID: 9855532
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Bilateral periventricular and subcortical heterotopia in a man with refractory epilepsy.
    Sisodiya SM; Free SL; Duncan JS; Stevens JM
    Epilepsia; 2000 Mar; 41(3):352-4. PubMed ID: 10714409
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Whole-exome sequencing of a unique brain malformation with periventricular heterotopia, cingulate polymicrogyria and midbrain tectal hyperplasia.
    Okumura A; Hayashi M; Shimojima K; Ikeno M; Uchida T; Takanashi J; Okamoto N; Hisata K; Shoji H; Saito A; Furukawa T; Kishida T; Shimizu T; Yamamoto T
    Neuropathology; 2013 Oct; 33(5):553-60. PubMed ID: 23240987
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects.
    de Wit MC; Kros JM; Halley DJ; de Coo IF; Verdijk R; Jacobs BC; Mancini GM
    J Neurol Neurosurg Psychiatry; 2009 Apr; 80(4):426-8. PubMed ID: 19289478
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Periventricular brain heterotopias in a child with adrenocortical insufficiency, achalasia, alacrima, and neurologic abnormalities (Allgrove syndrome).
    Zeharia A; Shuper A; Mimouni M; Kornreich L; Rachmel A; Lerman-Sagie T
    J Child Neurol; 1999 May; 14(5):331-4. PubMed ID: 10342602
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Grey matter heterotopia: an unusual association of intractable epilepsy.
    Stafford Johnson DB; Brennan P; Dwyer AJ; Toland J
    Ir J Med Sci; 1997; 166(3):135-8. PubMed ID: 9256546
    [TBL] [Abstract][Full Text] [Related]  

  • 71. A new missense mutation found in the FLNA gene in a family with bilateral periventricular nodular heterotopia (BPNH) alters the splicing process.
    Tsuneda SS; Torres FR; Montenegro MA; Guerreiro MM; Cendes F; Lopes-Cendes I
    J Mol Neurosci; 2008 Jun; 35(2):195-200. PubMed ID: 18427995
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Subcortical laminar heterotopia in two sisters and their mother: MRI, clinical findings and pathogenesis.
    van der Valk PH; Snoeck I; Meiners LC; des Portes V; Chelly J; Pinard JM; Ippel PF; van Nieuwenhuizen O; Peters AC
    Neuropediatrics; 1999 Jun; 30(3):155-60. PubMed ID: 10480213
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Assignment of human filamin gene FLNB to human chromosome band 3p14.3 and identification of YACs containing the complete FLNB transcribed region.
    Bröcker F; Bardenheuer W; Vieten L; Jülicher K; Werner N; Marquitan G; Michael D; Opalka B; Schütte J
    Cytogenet Cell Genet; 1999; 85(3-4):267-8. PubMed ID: 10449914
    [No Abstract]   [Full Text] [Related]  

  • 74. The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopia.
    Lu YT; Hsu CY; Liu YT; Chan CK; Chuang YC; Lin CH; Chang KP; Ho CJ; Ng CC; Lim KS; Tsai MH
    Biomed J; 2022 Jun; 45(3):542-548. PubMed ID: 35660364
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Male monozygotic twins discordant for periventricular nodular heterotopia and epilepsy.
    Sisodiya SM; Marques W; Everitt A; Sander JW
    Epilepsia; 1999 Feb; 40(2):248-50. PubMed ID: 9952275
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.
    Fink JM; Dobyns WB; Guerrini R; Hirsch BA
    Am J Hum Genet; 1997 Aug; 61(2):379-87. PubMed ID: 9311743
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Periventricular nodular heterotopia and dystonia due to an ARFGEF2 mutation.
    Bardón-Cancho EJ; Muñoz-Jiménez L; Vázquez-López M; Ruíz-Martín Y; García-Morín M; Barredo-Valderrama E
    Pediatr Neurol; 2014 Sep; 51(3):461-4. PubMed ID: 25160555
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Familial cardiac valvulopathy due to filamin A mutation.
    Bernstein JA; Bernstein D; Hehr U; Hudgins L
    Am J Med Genet A; 2011 Sep; 155A(9):2236-41. PubMed ID: 21815255
    [TBL] [Abstract][Full Text] [Related]  

  • 79. A new locus for familial temporal lobe epilepsy on chromosome 3q.
    Chahine L; Abou-Khalil B; Siren A; Andermann F; Hedera P; Ge Q; Andermann E; Pandolfo M
    Epilepsy Res; 2013 Oct; 106(3):338-44. PubMed ID: 24021842
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Patient with bilateral periventricular nodular heterotopia and polymicrogyria with apparently balanced reciprocal translocation t(1;6)(p12;p12.2) that interrupts the mannosidase alpha, class 1A, and glutathione S-transferase A2 genes.
    Leeflang EP; Marsh SE; Parrini E; Moro F; Pilz D; Dobyns WB; Guerrini R; Wheless JW; Gleeson JG
    J Med Genet; 2003 Dec; 40(12):e128. PubMed ID: 14684696
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.