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 *

133 related articles for article (PubMed ID: 7709734)

  • 1. Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brains.
    Gelot A; Billette de Villemeur T; Bordarier C; Ruchoux MM; Moraine C; Ponsot G
    Acta Neuropathol; 1995; 89(1):72-84. PubMed ID: 7709734
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Oculocerebral anomalies in Walker's lissencephaly].
    Robain O; Dhermy P; Dufier JL; Blanck MF; Dulac O; Bursztyn J
    J Fr Ophtalmol; 1985; 8(1):59-72. PubMed ID: 3923093
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fetal type II lissencephaly: a case report.
    Squier MV
    Childs Nerv Syst; 1993 Nov; 9(7):400-2. PubMed ID: 8306355
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Development of the cortical dysplasia of type II lissencephaly.
    Squier MV
    Neuropathol Appl Neurobiol; 1993 Jun; 19(3):209-13. PubMed ID: 8355808
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A.
    Fallet-Bianco C; Loeuillet L; Poirier K; Loget P; Chapon F; Pasquier L; Saillour Y; Beldjord C; Chelly J; Francis F
    Brain; 2008 Sep; 131(Pt 9):2304-20. PubMed ID: 18669490
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lissencephaly: two distinct clinico-pathological types.
    Dambska M; Wisniewski K; Sher JH
    Brain Dev; 1983; 5(3):302-10. PubMed ID: 6614389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Precocious cerebral development associated with agenesis of the corpus callosum in mid-fetal life: a transient syndrome?
    Hori A
    Acta Neuropathol; 1996; 91(1):120-5. PubMed ID: 8773157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotypically defined lissencephalies show distinct pathologies.
    Forman MS; Squier W; Dobyns WB; Golden JA
    J Neuropathol Exp Neurol; 2005 Oct; 64(10):847-57. PubMed ID: 16215456
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases.
    Pasquier L; Marcorelles P; Loget P; Pelluard F; Carles D; Perez MJ; Bendavid C; de La Rochebrochard C; Ferry M; David V; Odent S; Laquerrière A
    Acta Neuropathol; 2009 Feb; 117(2):185-200. PubMed ID: 19057916
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia.
    Miyata H; Chute DJ; Fink J; Villablanca P; Vinters HV
    Acta Neuropathol; 2004 Jan; 107(1):69-81. PubMed ID: 14566414
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Disorder of cerebellar foliation in Walker's lissencephaly and neu-laxova syndrome.
    Lyon G; Raymond G; Mogami K; Gadisseux JF; Della Giustina E
    J Neuropathol Exp Neurol; 1993 Nov; 52(6):633-9. PubMed ID: 8229082
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial lissencephaly with cleft palate and severe cerebellar hypoplasia.
    Kerner B; Graham JM; Golden JA; Pepkowitz SH; Dobyns WB
    Am J Med Genet; 1999 Dec; 87(5):440-5. PubMed ID: 10594886
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Walker-Warburg syndrome: report of three affected sibs.
    Rodgers BL; Vanner LV; Pai GS; Sens MA
    Am J Med Genet; 1994 Jan; 49(2):198-201. PubMed ID: 8116667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Agyria-pachygyria (lissencephaly syndrome).
    Jellinger K; Rett A
    Neuropadiatrie; 1976 Feb; 7(1):66-91. PubMed ID: 988918
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The mechanism of arrest of neuronal migration in the Zellweger malformation: an hypothesis bases upon cytoarchitectonic analysis.
    Evrard P; Caviness VS; Prats-Vinas J; Lyon G
    Acta Neuropathol; 1978 Feb; 41(2):109-17. PubMed ID: 636841
    [No Abstract]   [Full Text] [Related]  

  • 16. Lissencephaly with pontocerebellar hypoplasia.
    al Shawan SA; Bruyn GW; al Deeb SM
    J Child Neurol; 1996 May; 11(3):241-4. PubMed ID: 8734030
    [No Abstract]   [Full Text] [Related]  

  • 17. Microgyric and necrotic cortical lesions in twin fetuses: original cerebral damage consecutive to twinning?
    Bordarier C; Robain O
    Brain Dev; 1992 May; 14(3):174-8. PubMed ID: 1514658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pattern of childhood epilepsies with neuronal migrational disorders in Oman.
    Koul R; Jain R; Chacko A
    J Child Neurol; 2006 Nov; 21(11):945-9. PubMed ID: 17092459
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In utero MR imaging in fetuses at high risk of lissencephaly.
    Williams F; Griffiths PD
    Br J Radiol; 2017 Apr; 90(1072):20160902. PubMed ID: 28134568
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spatial and temporal development of the gliovascular tissue in type II lissencephaly.
    Bornemann A; Aigner T; Kirchner T
    Acta Neuropathol; 1997 Feb; 93(2):173-7. PubMed ID: 9039465
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.