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 *

148 related articles for article (PubMed ID: 18181206)

  • 1. Huntington's disease phenocopies are clinically and genetically heterogeneous.
    Wild EJ; Mudanohwo EE; Sweeney MG; Schneider SA; Beck J; Bhatia KP; Rossor MN; Davis MB; Tabrizi SJ
    Mov Disord; 2008 Apr; 23(5):716-20. PubMed ID: 18181206
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.
    Koutsis G; Karadima G; Pandraud A; Sweeney MG; Paudel R; Houlden H; Wood NW; Panas M
    J Neurol; 2012 Sep; 259(9):1874-8. PubMed ID: 22297462
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Huntington's disease phenocopy syndromes.
    Wild EJ; Tabrizi SJ
    Curr Opin Neurol; 2007 Dec; 20(6):681-7. PubMed ID: 17992089
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.
    Stevanin G; Fujigasaki H; Lebre AS; Camuzat A; Jeannequin C; Dode C; Takahashi J; San C; Bellance R; Brice A; Durr A
    Brain; 2003 Jul; 126(Pt 7):1599-603. PubMed ID: 12805114
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Huntington disease and Huntington disease-like in a case series from Brazil.
    Castilhos RM; Souza AF; Furtado GV; Gheno TC; Silva AL; Vargas FR; Lima MA; Barsottini O; Pedroso JL; Godeiro C; Salarini D; Pereira ET; Lin K; Toralles MB; Saute JA; Rieder CR; Quintas M; Sequeiros J; Alonso I; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2014 Oct; 86(4):373-7. PubMed ID: 24102565
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.
    Schneider SA; Walker RH; Bhatia KP
    Nat Clin Pract Neurol; 2007 Sep; 3(9):517-25. PubMed ID: 17805246
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.
    Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Hoffman-Zacharska D; Rajkiewicz M; Fidziańska E; Kowalska G; Zaremba J
    Neurol Neurochir Pol; 2008; 42(3):203-9. PubMed ID: 18651325
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Investigations of Huntington's Disease and Huntington's Disease-Like Syndromes in Indian Choreatic Patients.
    Kaur J; Parveen S; Shamim U; Sharma P; Suroliya V; Sonkar AK; Ahmad I; Garg J; Anand KS; Laskar S; Chowdhury D; Kushwaha S; Goyal V; Srivastava AK; Singh G; Faruq M
    J Huntingtons Dis; 2020; 9(3):283-289. PubMed ID: 32675418
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.
    Costa MDC; Teixeira-Castro A; Constante M; Magalhães M; Magalhães P; Cerqueira J; Vale J; Passão V; Barbosa C; Robalo C; Coutinho P; Barros J; Santos MM; Sequeiros J; Maciel P
    J Hum Genet; 2006; 51(8):645-651. PubMed ID: 16858508
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Huntington's Disease, Huntington's Disease Look-Alikes‎, and Benign Hereditary Chorea: What's New?
    Schneider SA; Bird T
    Mov Disord Clin Pract; 2016; 3(4):342-354. PubMed ID: 30713928
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Differential diagnosis of Huntington's disease: what the clinician should know.
    Cardoso F
    Neurodegener Dis Manag; 2014; 4(1):67-72. PubMed ID: 24640980
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Huntington's disease look-alikes.
    Schneider SA; Bhatia KP
    Handb Clin Neurol; 2011; 100():101-12. PubMed ID: 21496572
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation.
    Bech S; Petersen T; Nørremølle A; Gjedde A; Ehlers L; Eiberg H; Hjermind LE; Hasholt L; Lundorf E; Nielsen JE
    Parkinsonism Relat Disord; 2010 Jan; 16(1):12-5. PubMed ID: 19595623
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders.
    Paucar M; Laffita-Mesa J; Niemelä V; Malmgren H; Nennesmo I; Lagerstedt-Robinson K; Nordenskjöld M; Svenningsson P
    J Neurol Sci; 2023 Aug; 451():120707. PubMed ID: 37379724
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.
    Rodrigues GR; Walker RH; Bader B; Danek A; Brice A; Cazeneuve C; Russaouen O; Lopes-Cendes I; Marques W; Tumas V
    Arq Neuropsiquiatr; 2011 Jun; 69(3):419-23. PubMed ID: 21755114
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
    Mariani LL; Tesson C; Charles P; Cazeneuve C; Hahn V; Youssov K; Freeman L; Grabli D; Roze E; Noël S; Peuvion JN; Bachoud-Levi AC; Brice A; Stevanin G; Durr A
    JAMA Neurol; 2016 Sep; 73(9):1105-14. PubMed ID: 27400454
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Huntington's disease and Huntington's disease-like syndromes: an overview.
    Gövert F; Schneider SA
    Curr Opin Neurol; 2013 Aug; 26(4):420-7. PubMed ID: 23812307
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.
    Schneider SA; van de Warrenburg BP; Hughes TD; Davis M; Sweeney M; Wood N; Quinn NP; Bhatia KP
    Neurology; 2006 Nov; 67(9):1701-3. PubMed ID: 17101913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci.
    Baine FK; Peerbhai N; Krause A
    J Neurol Sci; 2018 Jul; 390():200-204. PubMed ID: 29801887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?
    Pedroso JL; de Freitas ME; Albuquerque MV; Saraiva-Pereira ML; Jardim LB; Barsottini OG
    J Neurol Sci; 2014 Dec; 347(1-2):356-8. PubMed ID: 25456461
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.