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 *

125 related articles for article (PubMed ID: 11071144)

  • 21. 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]  

  • 22. Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
    Gleeson JG; Minnerath SR; Fox JW; Allen KM; Luo RF; Hong SE; Berg MJ; Kuzniecky R; Reitnauer PJ; Borgatti R; Mira AP; Guerrini R; Holmes GL; Rooney CM; Berkovic S; Scheffer I; Cooper EC; Ricci S; Cusmai R; Crawford TO; Leroy R; Andermann E; Wheless JW; Dobyns WB; Walsh CA
    Ann Neurol; 1999 Feb; 45(2):146-53. PubMed ID: 9989615
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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. PubMed ID: 12185771
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel missense mutation of doublecortin: mutation analysis of Korean patients with subcortical band heterotopia.
    Kim MK; Park MS; Kim BC; Cho KH; Kim YS; Kim JH; Lee MC; Heo T; Kim EY
    J Korean Med Sci; 2005 Aug; 20(4):670-3. PubMed ID: 16100463
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cloning and developmental expression of the murine homolog of doublecortin.
    Matsuo N; Kawamoto S; Matsubara K; Okubo K
    Biochem Biophys Res Commun; 1998 Nov; 252(3):571-6. PubMed ID: 9837748
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Laminar heterotopic grey matter (double cortex) in a patient with late onset Lennox-Gastaut syndrome.
    Soucek D; Birbamer G; Luef G; Felber S; Kristmann E; Bauer G
    Wien Klin Wochenschr; 1992; 104(19):607-8. PubMed ID: 1441556
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q.
    Bisulli F; Tinuper P; Marini C; Avoni P; Carraro G; Nobile C
    Epileptic Disord; 2002 Sep; 4(3):183-7. PubMed ID: 12446220
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.
    D'Agostino MD; Bernasconi A; Das S; Bastos A; Valerio RM; Palmini A; Costa da Costa J; Scheffer IE; Berkovic S; Guerrini R; Dravet C; Ono J; Gigli G; Federico A; Booth F; Bernardi B; Volpi L; Tassinari CA; Guggenheim MA; Ledbetter DH; Gleeson JG; Lopes-Cendes I; Vossler DG; Malaspina E; Franzoni E; Sartori RJ; Mitchell MH; Mercho S; Dubeau F; Andermann F; Dobyns WB; Andermann E
    Brain; 2002 Nov; 125(Pt 11):2507-22. PubMed ID: 12390976
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia.
    Mei D; Parrini E; Pasqualetti M; Tortorella G; Franzoni E; Giussani U; Marini C; Migliarini S; Guerrini R
    Neurology; 2007 Feb; 68(6):446-50. PubMed ID: 17283321
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex.
    Scuderi C; Borgione E; Castello F; Lo Giudice M; Fichera M; Elia M; Amato C; Savio M; Di Blasi FD; Vitello GA; Romano S; DiMauro S; Musumeci SA
    Mitochondrion; 2010 Aug; 10(5):548-54. PubMed ID: 20433951
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Doublecortin Mutation in an Adolescent Male.
    Zare I; Paul D; Moody S
    Child Neurol Open; 2019; 6():2329048X19836589. PubMed ID: 31259193
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome.
    Schwartz CE; Gillessen-Kaesbach G; May M; Cappa M; Gorski J; Steindl K; Neri G
    Eur J Hum Genet; 2000 Nov; 8(11):869-74. PubMed ID: 11093277
    [TBL] [Abstract][Full Text] [Related]  

  • 36. X-linked pachygyria and agenesis of the corpus callosum: evidence for an X chromosome lissencephaly locus.
    Berry-Kravis E; Israel J
    Ann Neurol; 1994 Aug; 36(2):229-33. PubMed ID: 8053659
    [TBL] [Abstract][Full Text] [Related]  

  • 37. So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation.
    des Portes V; Abaoub L; Joannard A; Souville I; Francis F; Pinard JM; Chelly J; Beldjord C; Jouk PS
    Seizure; 2002 Jun; 11(4):273-7. PubMed ID: 12027577
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.
    Procopio R; Fortunato F; Gagliardi M; Talarico M; Sammarra I; Sarubbi MC; Malanga D; Annesi G; Gambardella A
    Int J Mol Sci; 2024 May; 25(10):. PubMed ID: 38791543
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nine novel L1 CAM mutations in families with X-linked hydrocephalus.
    MacFarlane JR; Du JS; Pepys ME; Ramsden S; Donnai D; Charlton R; Garrett C; Tolmie J; Yates JR; Berry C; Goudie D; Moncla A; Lunt P; Hodgson S; Jouet M; Kenwrick S
    Hum Mutat; 1997; 9(6):512-8. PubMed ID: 9195224
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genes that regulate neuronal migration in the cerebral cortex.
    Allen KM; Walsh CA
    Epilepsy Res; 1999 Sep; 36(2-3):143-54. PubMed ID: 10515162
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.