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 *

80 related articles for article (PubMed ID: 18809026)

  • 1. Subcortical laminar (band) heterotopia.
    Tanaka T; Gleeson JG
    Handb Clin Neurol; 2008; 87():191-204. PubMed ID: 18809026
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families.
    Passemard S; Gelot A; Fogli A; N'Guyen S; Barnerias C; Niel F; Doummar D; Arbues AS; Mignot C; de Villemeur TB; Ponsot G; Boespflug-Tanguy O; Rodriguez D
    Neurology; 2007 Jul; 69(4):400-2. PubMed ID: 17646634
    [No Abstract]   [Full Text] [Related]  

  • 4. Missense mutations resulting in type 1 lissencephaly.
    Reiner O; Coquelle FM
    Cell Mol Life Sci; 2005 Feb; 62(4):425-34. PubMed ID: 15719169
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. Leukoencephalopathy with ataxia, hypodontia, and hypomyelination.
    Wolf NI; Harting I; Boltshauser E; Wiegand G; Koch MJ; Schmitt-Mechelke T; Martin E; Zschocke J; Uhlenberg B; Hoffmann GF; Weber L; Ebinger F; Rating D
    Neurology; 2005 Apr; 64(8):1461-4. PubMed ID: 15851747
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NMDA receptor composition differs among anatomically diverse malformations of cortical development.
    Finardi A; Gardoni F; Bassanini S; Lasio G; Cossu M; Tassi L; Caccia C; Taroni F; LoRusso G; Di Luca M; Battaglia G
    J Neuropathol Exp Neurol; 2006 Sep; 65(9):883-93. PubMed ID: 16957582
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preserved episodic memory in subcortical band heterotopia.
    Janzen L; Sherman E; Langfitt J; Berg M; Connolly M
    Epilepsia; 2004 May; 45(5):555-8. PubMed ID: 15101838
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defects.
    Deconinck N; Duprez T; des Portes V; Beldjord C; Ghariani S; Sindic CJ; Sébire G
    Neuropediatrics; 2003 Jun; 34(3):146-8. PubMed ID: 12910438
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Susceptibility-weighted imaging in familial cerebral cavernous malformations.
    Cooper AD; Campeau NG; Meissner I
    Neurology; 2008 Jul; 71(5):382. PubMed ID: 18663188
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Neurological manifestations of the oculodentodigital dysplasia syndrome.
    Loddenkemper T; Grote K; Evers S; Oelerich M; Stögbauer F
    J Neurol; 2002 May; 249(5):584-95. PubMed ID: 12021949
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A remarkable pattern of subcortical vessel wall enhancement in granulomatous angiitis of the central nervous system.
    Schoenmaker N; Germans MR; Troost D; Richard E
    J Rheumatol; 2012 Oct; 39(10):2051-3. PubMed ID: 23028033
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 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. [Subcortical band heterotopia].
    Takeuchi Y
    Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):133-6. PubMed ID: 12483846
    [No Abstract]   [Full Text] [Related]  

  • 18. Protein-protein interactions, cytoskeletal regulation and neuronal migration.
    Feng Y; Walsh CA
    Nat Rev Neurosci; 2001 Jun; 2(6):408-16. PubMed ID: 11389474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Intrinsic epileptogenicity of an isolated periventricular nodular heterotopia.
    Scherer C; Schuele S; Minotti L; Chabardes S; Hoffmann D; Kahane P
    Neurology; 2005 Aug; 65(3):495-6. PubMed ID: 16087931
    [No Abstract]   [Full Text] [Related]  

  • 20. [Subcortical laminal heterotopia and lissencephaly: cerebral malformations of X-linked inheritance].
    Pinard JM; Desguerre I; Motte J; Dulac O; Ponsot G
    Rev Neurol (Paris); 1995 Mar; 151(3):171-6. PubMed ID: 7676153
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.