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 *

166 related articles for article (PubMed ID: 38394064)

  • 21. Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations.
    Accogli A; Severino M; Riva A; Madia F; Balagura G; Iacomino M; Carlini B; Baldassari S; Giacomini T; Croci C; Pisciotta L; Messana T; Boni A; Russo A; Bilo L; Tonziello R; Coppola A; Filla A; Mecarelli O; Casalone R; Pisani F; Falsaperla R; Marino S; Parisi P; Ferretti A; Elia M; Luchetti A; Milani D; Vanadia F; Silvestri L; Rebessi E; Parente E; Vatti G; Mancardi MM; Nobili L; Capra V; Salpietro V; Striano P; Zara F
    Seizure; 2020 Aug; 80():145-152. PubMed ID: 32570172
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita.
    Weber M; Jaber D; Encha-Razavi F; Julien E; Grevoul-Fesquet J; Steffann J; Melki J; Martinovic J
    Am J Med Genet A; 2022 Aug; 188(8):2331-2338. PubMed ID: 35686685
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Co-occurring malformations of cortical development and SCN1A gene mutations.
    Barba C; Parrini E; Coras R; Galuppi A; Craiu D; Kluger G; Parmeggiani A; Pieper T; Schmitt-Mechelke T; Striano P; Giordano F; Blumcke I; Guerrini R
    Epilepsia; 2014 Jul; 55(7):1009-19. PubMed ID: 24902755
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations.
    Guerrini R; Mei D; Cordelli DM; Pucatti D; Franzoni E; Parrini E
    Eur J Hum Genet; 2012 Sep; 20(9):995-8. PubMed ID: 22333901
    [TBL] [Abstract][Full Text] [Related]  

  • 25. X-linked malformations of cortical development.
    Leventer RJ; Mills PL; Dobyns WB
    Am J Med Genet; 2000; 97(3):213-20. PubMed ID: 11449490
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Bilateral posterior periventricular nodular heterotopia: a recognizable cortical malformation with a spectrum of associated brain abnormalities.
    Mandelstam SA; Leventer RJ; Sandow A; McGillivray G; van Kogelenberg M; Guerrini R; Robertson S; Berkovic SF; Jackson GD; Scheffer IE
    AJNR Am J Neuroradiol; 2013 Feb; 34(2):432-8. PubMed ID: 23348762
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Malformations of cortical development (MCDs) and epilepsy: experience from a tertiary care center in south India.
    Mathew T; Srikanth SG; Satishchandra P
    Seizure; 2010 Apr; 19(3):147-52. PubMed ID: 20144553
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Diffuse malformations of cortical development.
    Bahi-Buisson N; Guerrini R
    Handb Clin Neurol; 2013; 111():653-65. PubMed ID: 23622213
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
    Jaglin XH; Poirier K; Saillour Y; Buhler E; Tian G; Bahi-Buisson N; Fallet-Bianco C; Phan-Dinh-Tuy F; Kong XP; Bomont P; Castelnau-Ptakhine L; Odent S; Loget P; Kossorotoff M; Snoeck I; Plessis G; Parent P; Beldjord C; Cardoso C; Represa A; Flint J; Keays DA; Cowan NJ; Chelly J
    Nat Genet; 2009 Jun; 41(6):746-52. PubMed ID: 19465910
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genomic variants and variations in malformations of cortical development.
    Jamuar SS; Walsh CA
    Pediatr Clin North Am; 2015 Jun; 62(3):571-85. PubMed ID: 26022163
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Macro- and microscopic systematization of cerebral cortex malformations in children].
    Milovanov AP; Milovanova OA
    Arkh Patol; 2011; 73(5):23-7. PubMed ID: 22288167
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.
    Bahi-Buisson N; Poirier K; Boddaert N; Fallet-Bianco C; Specchio N; Bertini E; Caglayan O; Lascelles K; Elie C; Rambaud J; Baulac M; An I; Dias P; des Portes V; Moutard ML; Soufflet C; El Maleh M; Beldjord C; Villard L; Chelly J
    Brain; 2010 Nov; 133(11):3194-209. PubMed ID: 20929962
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Tuberous sclerosis complex with unilateral perisylvian polymicrogyria and contralateral hippocampal sclerosis - a case report.
    Helbok R; Kuchukhidze G; Unterberger I; Koppelstaetter F; Dobesberger J; Donnemiller E; Trinka E
    Seizure; 2009 May; 18(4):303-5. PubMed ID: 19128987
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Malformations of cortical development: molecular pathogenesis and experimental strategies.
    Crino PB
    Adv Exp Med Biol; 2004; 548():175-91. PubMed ID: 15250594
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Tubulin mutations in human neurodevelopmental disorders.
    Maillard C; Roux CJ; Charbit-Henrion F; Steffann J; Laquerriere A; Quazza F; Buisson NB
    Semin Cell Dev Biol; 2023 Mar; 137():87-95. PubMed ID: 35915025
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Tensor-valued diffusion MRI differentiates cortex and white matter in malformations of cortical development associated with epilepsy.
    Lampinen B; Zampeli A; Björkman-Burtscher IM; Szczepankiewicz F; Källén K; Compagno Strandberg M; Nilsson M
    Epilepsia; 2020 Aug; 61(8):1701-1713. PubMed ID: 32667688
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Malformations of cortical development.
    Pang T; Atefy R; Sheen V
    Neurologist; 2008 May; 14(3):181-91. PubMed ID: 18469675
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.