BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 19530012)

  • 1. Huntington's disease presenting as amyotrophic lateral sclerosis.
    Phukan J; Ali E; Pender NP; Molloy F; Hennessy M; Walsh RJ; Hardiman O
    Amyotroph Lateral Scler; 2010 Aug; 11(4):405-7. PubMed ID: 19530012
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Importance of the number of trinucleotide repeat expansions in the clinical manifestations of Huntington's chorea].
    Vojvodić N; Culjković B; Romac S; Stojković O; Sternić N; Sokić D; Kostić VS
    Srp Arh Celok Lek; 1998; 126(3-4):77-82. PubMed ID: 9863360
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Huntington chorea presenting with motor neuron disease.
    Sadeghian H; O'Suilleabhain PE; Battiste J; Elliott JL; Trivedi JR
    Arch Neurol; 2011 May; 68(5):650-2. PubMed ID: 21555641
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comment on 'Huntington's disease presenting as ALS'.
    Mandrioli J; Bernabei C; Georgoulopoulou E; Nichelli P; Cortelli P; Tupler R; Signaroldi E; Sola P
    Amyotroph Lateral Scler; 2010 Aug; 11(4):408-9. PubMed ID: 20001577
    [No Abstract]   [Full Text] [Related]  

  • 5. Genetically confirmed Huntington's disease masquerading as motor neuron disease.
    Kanai K; Kuwabara S; Sawai S; Nakata M; Misawa S; Isose S; Hirano S; Kawaguchi N; Katayama K; Hattori T
    Mov Disord; 2008 Apr; 23(5):748-51. PubMed ID: 18186118
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Huntington's chorea: clinical aspects, genetics and current diagnosis].
    Spiegel R
    Ther Umsch; 1995 Dec; 52(12):814-20. PubMed ID: 8539653
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Familial amyotrophic lateral sclerosis associated with Huntington chorea with increased aspartate level in the cerebrospinal fluid].
    Blin O; Samuel D; Guieu R; Pouget J; Nieoullon A; Serratrice G
    Rev Neurol (Paris); 1992; 148(2):144-6. PubMed ID: 1534926
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genetic advances in neurodegenerative disorders.
    Aguilera AJ
    Clin Lab Med; 1995 Dec; 15(4):915-26. PubMed ID: 8838230
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chorea-ballism associated with familial amyotrophic lateral sclerosis. A clinical, genetic, and neuropathological study.
    Gamez J; Corbera-Bellalta M; Mila M; López-Lisbona R; Boluda S; Ferrer I
    Mov Disord; 2008 Feb; 23(3):434-8. PubMed ID: 18072201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of the Huntington's disease gene in New Zealand.
    Whitefield JE; Williams L; Snow K; Dixon J; Winship I; Stapleton PM; Faull RM; Love DR
    N Z Med J; 1996 Feb; 109(1015):27-30. PubMed ID: 8606810
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects].
    Illarioshkin SN; Ivanova-Smolenskaia IA; Markova ED; Nikol'skaia NN; Chabrashvili TZ; Insarova NG
    Genetika; 1996 Jan; 32(1):103-9. PubMed ID: 8647411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diffusion tensor MRI of early upper motor neuron involvement in amyotrophic lateral sclerosis.
    Sach M; Winkler G; Glauche V; Liepert J; Heimbach B; Koch MA; Büchel C; Weiller C
    Brain; 2004 Feb; 127(Pt 2):340-50. PubMed ID: 14607785
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tourettism associated with Huntington's disease.
    Jankovic J; Ashizawa T
    Mov Disord; 1995 Jan; 10(1):103-5. PubMed ID: 7885343
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Atypical motor neuron disease and related motor syndromes.
    Verma A; Bradley WG
    Semin Neurol; 2001 Jun; 21(2):177-87. PubMed ID: 11442326
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis.
    Jih KY; Lai KL; Lin KP; Liao YC; Lee YC
    J Chin Med Assoc; 2023 Jan; 86(1):47-51. PubMed ID: 36599142
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular diagnosis in Huntington's disease].
    Rosales-Reynoso MA; Barros-Núñez P
    Gac Med Mex; 2008; 144(3):271-3. PubMed ID: 18714598
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Awaji diagnostic algorithm increases sensitivity of El Escorial criteria for ALS diagnosis.
    Carvalho MD; Swash M
    Amyotroph Lateral Scler; 2009 Feb; 10(1):53-7. PubMed ID: 18985466
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Coexistence of Huntington's disease and familial amyotrophic lateral sclerosis: case presentation.
    Rubio A; Steinberg K; Figlewicz DA; MacDonald ME; Greenamyre T; Hamill R; Shoulson I; Powers JM
    Acta Neuropathol; 1996 Oct; 92(4):421-7. PubMed ID: 8891076
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up.
    Tartaglia MC; Rowe A; Findlater K; Orange JB; Grace G; Strong MJ
    Arch Neurol; 2007 Feb; 64(2):232-6. PubMed ID: 17296839
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.