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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]
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]