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 *

107 related articles for article (PubMed ID: 19433673)

  • 1. No association between SRGAP3/MEGAP haploinsufficiency and mental retardation.
    Hamdan FF; Gauthier J; Pellerin S; Dobrzeniecka S; Marineau C; Fombonne E; Mottron L; Lafrenière RG; Drapeau P; Lacaille JC; Rouleau GA; Michaud JL
    Arch Neurol; 2009 May; 66(5):675-6. PubMed ID: 19433673
    [No Abstract]   [Full Text] [Related]  

  • 2. The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation.
    Endris V; Wogatzky B; Leimer U; Bartsch D; Zatyka M; Latif F; Maher ER; Tariverdian G; Kirsch S; Karch D; Rappold GA
    Proc Natl Acad Sci U S A; 2002 Sep; 99(18):11754-9. PubMed ID: 12195014
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association between PTGS2 polymorphism and autism spectrum disorders in Korean trios.
    Yoo HJ; Cho IH; Park M; Cho E; Cho SC; Kim BN; Kim JW; Kim SA
    Neurosci Res; 2008 Sep; 62(1):66-9. PubMed ID: 18579107
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Glycine decarboxylase mutations: a distinctive phenotype of nonketotic hyperglycinemia in adults.
    Dinopoulos A; Kure S; Chuck G; Sato K; Gilbert DL; Matsubara Y; Degrauw T
    Neurology; 2005 Apr; 64(7):1255-7. PubMed ID: 15824356
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High frequency of creatine deficiency syndromes in patients with unexplained mental retardation.
    Lion-François L; Cheillan D; Pitelet G; Acquaviva-Bourdain C; Bussy G; Cotton F; Guibaud L; Gérard D; Rivier C; Vianey-Saban C; Jakobs C; Salomons GS; des Portes V
    Neurology; 2006 Nov; 67(9):1713-4. PubMed ID: 17101918
    [No Abstract]   [Full Text] [Related]  

  • 6. A mutation in adenylosuccinate lyase associated with mental retardation and autistic features.
    Stone RL; Aimi J; Barshop BA; Jaeken J; Van den Berghe G; Zalkin H; Dixon JE
    Nat Genet; 1992 Apr; 1(1):59-63. PubMed ID: 1302001
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Neurological findings in aminoacylase 1 deficiency.
    Sass JO; Olbrich H; Mohr V; Hart C; Woldseth B; Krywawych S; Bjurulf B; Lakhani PK; Buchdahl RM; Omran H
    Neurology; 2007 Jun; 68(24):2151-3. PubMed ID: 17562838
    [No Abstract]   [Full Text] [Related]  

  • 8. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease.
    Brouwers N; Sleegers K; Engelborghs S; Maurer-Stroh S; Gijselinck I; van der Zee J; Pickut BA; Van den Broeck M; Mattheijssens M; Peeters K; Schymkowitz J; Rousseau F; Martin JJ; Cruts M; De Deyn PP; Van Broeckhoven C
    Neurology; 2008 Aug; 71(9):656-64. PubMed ID: 18565828
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic association between polymorphisms in the BTG1 gene and multiple sclerosis.
    Camiña-Tato M; Morcillo-Suárez C; Navarro A; Fernández M; Horga A; Montalban X; Comabella M
    J Neuroimmunol; 2009 Aug; 213(1-2):142-7. PubMed ID: 19515430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked oligophrenic vermian dysgenesis: syndromic vs non-syndromic X-linked mental retardation?
    Higgins JJ; Topaloglu H
    Neurology; 2005 Nov; 65(9):1346-7. PubMed ID: 16275817
    [No Abstract]   [Full Text] [Related]  

  • 11. Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.
    Yan J; Oliveira G; Coutinho A; Yang C; Feng J; Katz C; Sram J; Bockholt A; Jones IR; Craddock N; Cook EH; Vicente A; Sommer SS
    Mol Psychiatry; 2005 Apr; 10(4):329-32. PubMed ID: 15622415
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetic polymorphism at codon 129 of the prion protein gene is not associated with multiple sclerosis.
    Stüve O; Korth C; Gabatto P; Cameron EM; Hu W; Eagar TN; Monson NL; Frohman EM; Racke MK; Zabetian CP; Oksenberg JR
    Arch Neurol; 2009 Feb; 66(2):280-1. PubMed ID: 19204171
    [No Abstract]   [Full Text] [Related]  

  • 13. Association of pyridoxal kinase and Parkinson disease.
    Vilariño-Güell C; Wider C; Aasly JO; White LR; Rajput A; Rajput AH; Lynch T; Krygowska-Wajs A; Jasinska-Myga B; Opala G; Barcikowska M; Czyzewski K; Wu RM; Uitti RJ; Wszolek ZK; Farrer MJ; Ross OA
    Ann Neurol; 2010 Mar; 67(3):409-11. PubMed ID: 20373354
    [No Abstract]   [Full Text] [Related]  

  • 14. Autism genetics: strategies, challenges, and opportunities.
    O'Roak BJ; State MW
    Autism Res; 2008 Feb; 1(1):4-17. PubMed ID: 19360646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic analysis of genealogies in mentally retarded autistic probands from Saguenay Lac-Saint-Jean (Quebec, Canada).
    De Braekeleer M; Tremblay M; Thivierge J
    Ann Genet; 1996; 39(1):47-50. PubMed ID: 9297444
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Consequences of mutations within the C terminus of the FHL1 gene.
    Schoser B; Goebel HH; Janisch I; Quasthoff S; Rother J; Bergmann M; Müller-Felber W; Windpassinger C
    Neurology; 2009 Aug; 73(7):543-51. PubMed ID: 19687455
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autism and adenylosuccinase deficiency.
    Stathis SL; Cowley DM; Broe D
    J Am Acad Child Adolesc Psychiatry; 2000 Mar; 39(3):274-5. PubMed ID: 10714045
    [No Abstract]   [Full Text] [Related]  

  • 19. Genome structural variation and sporadic disease traits.
    Lupski JR
    Nat Genet; 2006 Sep; 38(9):974-6. PubMed ID: 16941003
    [No Abstract]   [Full Text] [Related]  

  • 20. Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations.
    Labauge P; Fontaine B; Neau JP; Bergametti F; Riant F; Blecon A; Marchelli F; Arnoult M; Lannuzel A; Clanet M; Olschwang S; Denier C; Tournier-Lasserve E
    Neurology; 2009 Jun; 72(23):2044-6. PubMed ID: 19506228
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.