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 *

187 related articles for article (PubMed ID: 17239055)

  • 1. Psychotic symptoms, epilepsy, mental retardation, and brain malformation in a patient with 45,XO/46,XX mosaicism: detection of mutation of ARX molecule.
    Fukuda K; Wakuda T; Kageyama M; Kitamura K; Tanaka M; Tawata Y; Miyauchi T; Ishida S
    Psychiatry Clin Neurosci; 2007 Feb; 61(1):134. PubMed ID: 17239055
    [No Abstract]   [Full Text] [Related]  

  • 2. Mosaic trisomy r(14) associated with epilepsy and mental retardation.
    Tzoufi M; Kanioglou C; Dasoula A; Asproudis I; Tsatsoulis A; Sismani C; Patsalis PC; Georgiou I; Syrrou M
    J Child Neurol; 2007 Jul; 22(7):869-73. PubMed ID: 17715281
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations.
    Dibbens LM; Kneen R; Bayly MA; Heron SE; Arsov T; Damiano JA; Desai T; Gibbs J; McKenzie F; Mulley JC; Ronan A; Scheffer IE
    Neurology; 2011 Apr; 76(17):1514-9. PubMed ID: 21519002
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.
    Kitamura K; Itou Y; Yanazawa M; Ohsawa M; Suzuki-Migishima R; Umeki Y; Hohjoh H; Yanagawa Y; Shinba T; Itoh M; Nakamura K; Goto Y
    Hum Mol Genet; 2009 Oct; 18(19):3708-24. PubMed ID: 19605412
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Familial study of patients with psychosis, epilepsy and mental retardation].
    Liu XH
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Apr; 16(2):99-102. PubMed ID: 6617371
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. Somatic mosaicism as a basic epileptogenic mechanism?
    Lindhout D
    Brain; 2008 Apr; 131(Pt 4):900-1. PubMed ID: 18339639
    [No Abstract]   [Full Text] [Related]  

  • 8. De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
    Hamdan FF; Piton A; Gauthier J; Lortie A; Dubeau F; Dobrzeniecka S; Spiegelman D; Noreau A; Pellerin S; Côté M; Henrion E; Fombonne E; Mottron L; Marineau C; Drapeau P; Lafrenière RG; Lacaille JC; Rouleau GA; Michaud JL
    Ann Neurol; 2009 Jun; 65(6):748-53. PubMed ID: 19557857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [2 cases of triplo-X with epileptic seizure].
    Takei H; Asaka A; Kurihara T
    No To Shinkei; 1969 May; 21(5):523-32. PubMed ID: 5394316
    [No Abstract]   [Full Text] [Related]  

  • 10. Unusual clinical syndrome in a boy with 45,X/46,XY mosaicism.
    Lespinasse J; Murthy S; Lesca G; Palfreeman N; Lemeyre E
    Genet Couns; 2005; 16(1):109-11. PubMed ID: 15844789
    [No Abstract]   [Full Text] [Related]  

  • 11. Epilepsy and mental retardation limited to females: an under-recognized disorder.
    Scheffer IE; Turner SJ; Dibbens LM; Bayly MA; Friend K; Hodgson B; Burrows L; Shaw M; Wei C; Ullmann R; Ropers HH; Szepetowski P; Haan E; Mazarib A; Afawi Z; Neufeld MY; Andrews PI; Wallace G; Kivity S; Lev D; Lerman-Sagie T; Derry CP; Korczyn AD; Gecz J; Mulley JC; Berkovic SF
    Brain; 2008 Apr; 131(Pt 4):918-27. PubMed ID: 18234694
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Psychological manifestations of epilepsy in childhood].
    Artigas J
    Rev Neurol; 1999 Feb; 28 Suppl 2():S135-41. PubMed ID: 10778503
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Facioscapulohumeral muscular dystrophy with severe mental retardation and epilepsy.
    Saito Y; Miyashita S; Yokoyama A; Komaki H; Seki A; Maegaki Y; Ohno K
    Brain Dev; 2007 May; 29(4):231-3. PubMed ID: 17010549
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome.
    Frints SG; Froyen G; Marynen P; Willekens D; Legius E; Fryns JP
    Am J Med Genet; 2002 Nov; 112(4):427-8. PubMed ID: 12376949
    [No Abstract]   [Full Text] [Related]  

  • 15. Mowat-Wilson syndrome affecting 3 siblings.
    Ohtsuka M; Oguni H; Ito Y; Nakayama T; Matsuo M; Osawa M; Saito K; Yamada Y; Wakamatsu N
    J Child Neurol; 2008 Mar; 23(3):274-8. PubMed ID: 18230842
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of 45,XO/47,XYY mosaicism with psychotic symptoms and neuroleptic malignant syndrome.
    Matsumoto T; Shiroyama T; Komori T; Inui K
    Prog Neuropsychopharmacol Biol Psychiatry; 2007 Jun; 31(5):1143-4. PubMed ID: 17478025
    [No Abstract]   [Full Text] [Related]  

  • 17. Expansion of the first polyalanine tract of the ARX gene in a boy presenting with generalized dystonia in the absence of infantile spasms.
    Shinozaki Y; Osawa M; Sakuma H; Komaki H; Nakagawa E; Sugai K; Sasaki M; Goto Y
    Brain Dev; 2009 Jun; 31(6):469-72. PubMed ID: 18823727
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A case of inv dup (15) mosaic with mental retardation and symptomatic generalized epilepsy].
    Kobayashi Y; Yoshino A
    No To Shinkei; 1999 Mar; 51(3):259-62. PubMed ID: 10226291
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaicism and phenotype in ring chromosome 20 syndrome.
    Nishiwaki T; Hirano M; Kumazawa M; Ueno S
    Acta Neurol Scand; 2005 Mar; 111(3):205-8. PubMed ID: 15691292
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Associated neuropsychiatric problems in Swedish school children with mild mental retardation.
    Gillberg C
    Ups J Med Sci Suppl; 1987; 44():111-4. PubMed ID: 3481893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.