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 *

234 related articles for article (PubMed ID: 9810565)

  • 1. X-linked subcortical laminar heterotopia and lissencephaly: a new family.
    Puche A; Rodriguez T; Domingo R; Casas C; Vicente T; Martinez-Lage JF
    Neuropediatrics; 1998 Oct; 29(5):276-8. PubMed ID: 9810565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial neuronal migration disorder: subcortical laminar heterotopia in a mother and pachygyria in the son.
    Toyama J; Kasuya H; Higuchi S; Kondo H; Naganuma Y; Uchiyama M
    Am J Med Genet; 1998 Feb; 75(5):481-4. PubMed ID: 9489790
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. 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]  

  • 5. Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.
    Pinard JM; Motte J; Chiron C; Brian R; Andermann E; Dulac O
    J Neurol Neurosurg Psychiatry; 1994 Aug; 57(8):914-20. PubMed ID: 8057113
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.
    Guerreiro MM; Andermann E; Guerrini R; Dobyns WB; Kuzniecky R; Silver K; Van Bogaert P; Gillain C; David P; Ambrosetto G; Rosati A; Bartolomei F; Parmeggiani A; Paetau R; Salonen O; Ignatius J; Borgatti R; Zucca C; Bastos AC; Palmini A; Fernandes W; Montenegro MA; Cendes F; Andermann F
    Ann Neurol; 2000 Jul; 48(1):39-48. PubMed ID: 10894214
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple pterygium syndrome, bilateral periventricular nodular heterotopia and epileptic seizures--a syndrome?
    Holtmann M; Woermann FG; Boenigk HE
    Neuropediatrics; 2001 Oct; 32(5):264-6. PubMed ID: 11748498
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked lissencephaly in an Indian family.
    Panda S; Tripathi M; Jain S; Sharma P
    Neurol India; 2003 Sep; 51(3):392-3. PubMed ID: 14652450
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.
    des Portes V; Pinard JM; Smadja D; Motte J; Boespflüg-Tanguy O; Moutard ML; Desguerre I; Billuart P; Carrie A; Bienvenu T; Vinet MC; Bachner L; Beldjord C; Dulac O; Kahn A; Ponsot G; Chelly J
    J Med Genet; 1997 Mar; 34(3):177-83. PubMed ID: 9132485
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations.
    Guerrini R; Moro F; Andermann E; Hughes E; D'Agostino D; Carrozzo R; Bernasconi A; Flinter F; Parmeggiani L; Volzone A; Parrini E; Mei D; Jarosz JM; Morris RG; Pratt P; Tortorella G; Dubeau F; Andermann F; Dobyns WB; Das S
    Ann Neurol; 2003 Jul; 54(1):30-7. PubMed ID: 12838518
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria).
    Ozmen M; Yilmaz Y; Calişkan M; Minareci O; Aydinli N
    Turk J Pediatr; 2000; 42(3):210-4. PubMed ID: 11105619
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Periventricular nodular and subcortical neuronal heterotopia in adult epileptic patients.
    Consalvo DE; Kochen SS; Alurralde A; Centurion E; Salgado PA; Saidon P; Sica RE
    Medicina (B Aires); 2006; 66(2):101-7. PubMed ID: 16715756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Neuronal migration disorders. Radiological and clinical aspects].
    Orderud WJ; Skjeldal OH; Strømme P
    Tidsskr Nor Laegeforen; 1995 Jun; 115(16):1952-6. PubMed ID: 7638849
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.
    Dobyns WB; Berry-Kravis E; Havernick NJ; Holden KR; Viskochil D
    Am J Med Genet; 1999 Oct; 86(4):331-7. PubMed ID: 10494089
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical picture of neuroblast migratory disorders].
    Flores-Dinorin L
    Rev Neurol; 1999 May 16-31; 28(10):990-6. PubMed ID: 10416238
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Pachygyria and laminar heterotopic tissue. A rare case of unique expression of a neuronal migration disorder in twins].
    Hebing B; Uhlenbrock D; Wesseler K
    Monatsschr Kinderheilkd; 1992 Apr; 140(4):220-2. PubMed ID: 1614447
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Cortical dysplasias and epilepsy].
    Peña JA
    Invest Clin; 2000 Mar; 41(1):59-71. PubMed ID: 10758699
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Age-related clinical and neurophysiologic characteristics of intractable epilepsy associated with cortical malformation.
    Kobayashi K; Ohtsuka Y; Ohno S; Tanaka A; Hiraki Y; Oka E
    Epilepsia; 2001; 42 Suppl 6():24-8. PubMed ID: 11902317
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.