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 *

131 related articles for article (PubMed ID: 32127224)

  • 1. Frequent Awakenings and Fits With Aerobics.
    Miller D; Kremer K
    Pediatr Neurol; 2020 May; 106():72-73. PubMed ID: 32127224
    [No Abstract]   [Full Text] [Related]  

  • 2. Paternal transmission of subcortical band heterotopia through DCX somatic mosaicism.
    Moreira I; Bastos-Ferreira R; Silva J; Ribeiro C; Alonso I; Chaves J
    Seizure; 2015 Feb; 25():62-4. PubMed ID: 25645638
    [No Abstract]   [Full Text] [Related]  

  • 3. Mosaic DCX deletion causes subcortical band heterotopia in males.
    Quélin C; Saillour Y; Souville I; Poirier K; N'guyen-Morel MA; Vercueil L; Millisher-Bellaiche AE; Boddaert N; Dubois F; Chelly J; Beldjord C; Bahi-Buisson N
    Neurogenetics; 2012 Nov; 13(4):367-73. PubMed ID: 22833188
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A male case of subcortical band heterotopia with somatic mosaicism of DCX mutation].
    Igarashi A; Kawatani M; Ohta G; Kometani H; Ohshima Y; Kato M
    No To Hattatsu; 2013 Sep; 45(5):371-4. PubMed ID: 24205692
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Incontinentia pigmenti with subcortical band heterotopias].
    Aoun A; Goizet C; Arveiler B; Sarrazin E; Derancourt C
    Arch Pediatr; 2015 Jan; 22(1):109-10. PubMed ID: 25435274
    [No Abstract]   [Full Text] [Related]  

  • 6. Novel human pathological mutations. Gene symbol: DCX. Disease: double cortex syndrome.
    Ellison J
    Hum Genet; 2010 Apr; 127(4):475. PubMed ID: 21488284
    [No Abstract]   [Full Text] [Related]  

  • 7. Teaching NeuroImages: Double cortex: Rare diagnosis in adulthood.
    Ikeda KM; Mirsattari SM
    Neurology; 2018 Oct; 91(18):e1724-e1725. PubMed ID: 30373929
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.
    Tsai MH; Kuo PW; Myers CT; Li SW; Lin WC; Fu TY; Chang HY; Mefford HC; Chang YC; Tsai JW
    Eur J Paediatr Neurol; 2016 Sep; 20(5):788-94. PubMed ID: 27292316
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia.
    Delatycki MB; Leventer RJ
    Eur J Hum Genet; 2009 Jun; 17(6):701-2. PubMed ID: 19050725
    [No Abstract]   [Full Text] [Related]  

  • 10. Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother.
    Takeshita S; Higuchi M; Suyama M; Koide W; Maki K; Ushijima K; Ban K; Saito M; Kato M; Saitoh S
    Pediatr Int; 2015 Apr; 57(2):321-3. PubMed ID: 25868952
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Analysis of DCX gene mutation in a patient featuring X-linked subcortical laminar heterotopia and epilepsy].
    Li W; Zhang MP; Hou ZJ; Zeng T; Tang B; Liu XR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):74-8. PubMed ID: 23450485
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Case of 1-year-old boy who developed intractable convulsions since birth].
    Miyata R
    No To Hattatsu; 2009 Mar; 41(2):81-2. PubMed ID: 19517769
    [No Abstract]   [Full Text] [Related]  

  • 13. Pigmentary mosaicism, subcortical band heterotopia, and brain cystic lesions.
    Ruggieri M; Roggini M; Spalice A; Addis M; Iannetti P
    Pediatr Neurol; 2009 May; 40(5):383-6. PubMed ID: 19380077
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interictal hypermetabolic subcortical band on brain FDG-PET in doublecortin mutation.
    Fong J; Wu G; Wyllie E; Gupta A
    Neurology; 2008 Aug; 71(7):535. PubMed ID: 18695165
    [No Abstract]   [Full Text] [Related]  

  • 15. New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.
    Bahi-Buisson N; Souville I; Fourniol FJ; Toussaint A; Moores CA; Houdusse A; Lemaitre JY; Poirier K; Khalaf-Nazzal R; Hully M; Leger PL; Elie C; Boddaert N; Beldjord C; Chelly J; Francis F;
    Brain; 2013 Jan; 136(Pt 1):223-44. PubMed ID: 23365099
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diffuse subcortical band heterotopia, periodic limb movements during sleep and a novel "de novo" mutation in the DCX gene.
    Parisi P; Miano S; Mei D; Paolino MC; Castaldo R; Villa MP
    Brain Dev; 2010 Jun; 32(6):511-5. PubMed ID: 19619967
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel missense mutation in LIS1 in a child with subcortical band heterotopia and pachygyria inherited from his mildly affected mother with somatic mosaicism.
    Mineyko A; Doja A; Hurteau J; Dobyns WB; Das S; Boycott KM
    J Child Neurol; 2010 Jun; 25(6):738-41. PubMed ID: 19808989
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The location of DCX mutations predicts malformation severity in X-linked lissencephaly.
    Leger PL; Souville I; Boddaert N; Elie C; Pinard JM; Plouin P; Moutard ML; des Portes V; Van Esch H; Joriot S; Renard JL; Chelly J; Francis F; Beldjord C; Bahi-Buisson N
    Neurogenetics; 2008 Oct; 9(4):277-85. PubMed ID: 18685874
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Normotopic cortex is the major contributor to epilepsy in experimental double cortex.
    Petit LF; Jalabert M; Buhler E; Malvache A; Peret A; Chauvin Y; Watrin F; Represa A; Manent JB
    Ann Neurol; 2014 Sep; 76(3):428-42. PubMed ID: 25074818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Classical (type I) lissencephaly and Miller-Dieker syndrome.
    Matarese CA; Renaud DL
    Pediatr Neurol; 2009 Apr; 40(4):324-5. PubMed ID: 19302951
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.