BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

278 related articles for article (PubMed ID: 23622213)

  • 1. 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]  

  • 2. [Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing].
    Bahi-Buisson N; Boddaert N; Saillour Y; Souville I; Poirier K; Léger PL; Castelnau L; Plouin P; Carion N; Beldjord C; Chelly J
    Rev Neurol (Paris); 2008 Dec; 164(12):995-1009. PubMed ID: 18808783
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
    Guerrini R; Carrozzo R
    Seizure; 2001 Oct; 10(7):532-43; quiz 544-7. PubMed ID: 11749114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Epilepsy and malformations of the cerebral cortex.
    Guerrini R; Sicca F; Parmeggiani L
    Epileptic Disord; 2003 Sep; 5 Suppl 2():S9-26. PubMed ID: 14617417
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Neuronal migration disorders.
    Guerrini R; Parrini E
    Neurobiol Dis; 2010 May; 38(2):154-66. PubMed ID: 19245832
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.
    Ross ME; Swanson K; Dobyns WB
    Neuropediatrics; 2001 Oct; 32(5):256-63. PubMed ID: 11748497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The wide spectrum of tubulinopathies: what are the key features for the diagnosis?
    Bahi-Buisson N; Poirier K; Fourniol F; Saillour Y; Valence S; Lebrun N; Hully M; Bianco CF; Boddaert N; Elie C; Lascelles K; Souville I; ; Beldjord C; Chelly J
    Brain; 2014 Jun; 137(Pt 6):1676-700. PubMed ID: 24860126
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuronal migration disorders: clinical, neuroradiologic and genetics aspects.
    Spalice A; Parisi P; Nicita F; Pizzardi G; Del Balzo F; Iannetti P
    Acta Paediatr; 2009 Mar; 98(3):421-33. PubMed ID: 19120042
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic Basis of Brain Malformations.
    Parrini E; Conti V; Dobyns WB; Guerrini R
    Mol Syndromol; 2016 Sep; 7(4):220-233. PubMed ID: 27781032
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Overlapping cortical malformations and mutations in TUBB2B and TUBA1A.
    Cushion TD; Dobyns WB; Mullins JG; Stoodley N; Chung SK; Fry AE; Hehr U; Gunny R; Aylsworth AS; Prabhakar P; Uyanik G; Rankin J; Rees MI; Pilz DT
    Brain; 2013 Feb; 136(Pt 2):536-48. PubMed ID: 23361065
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Malformations of cortical development and epilepsy, part 1: diagnosis and classification scheme.
    Kuzniecky RI
    Rev Neurol Dis; 2006; 3(4):151-62. PubMed ID: 17224898
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.
    Mokánszki A; Körhegyi I; Szabó N; Bereg E; Gergev G; Balogh E; Bessenyei B; Sümegi A; Morris-Rosendahl DJ; Sztriha L; Oláh E
    J Child Neurol; 2012 Dec; 27(12):1534-40. PubMed ID: 22408144
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.