BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

379 related articles for article (PubMed ID: 23538602)

  • 21. The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.
    Di Donato S; Gellera C; Mariotti C
    Neurol Sci; 2001 Jun; 22(3):219-28. PubMed ID: 11731874
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case series of hereditary cerebellar ataxias in a highly consanguineous population from Northeast Brazil.
    Rangel DM; Nóbrega PR; Saraiva-Pereira ML; Jardim LB; Braga-Neto P
    Parkinsonism Relat Disord; 2019 Apr; 61():193-197. PubMed ID: 30389370
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cerebellar/spinocerebellar syndromes.
    Mariotti C; Di Donato S
    Neurol Sci; 2001 Nov; 22 Suppl 2():S88-92. PubMed ID: 11794486
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Diagnosis and management of early- and late-onset cerebellar ataxia.
    Brusse E; Maat-Kievit JA; van Swieten JC
    Clin Genet; 2007 Jan; 71(1):12-24. PubMed ID: 17204042
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spinocerebellar degenerations.
    Perlman SL
    Handb Clin Neurol; 2011; 100():113-40. PubMed ID: 21496573
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
    Babovic-Vuksanovic D; Snow K; Patterson MC; Michels VV
    Am J Med Genet; 1998 Oct; 79(5):383-7. PubMed ID: 9779806
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prevalence of inherited ataxias in the province of Padua, Italy.
    Zortea M; Armani M; Pastorello E; Nunez GF; Lombardi S; Tonello S; Rigoni MT; Zuliani L; Mostacciuolo ML; Gellera C; Di Donato S; Trevisan CP
    Neuroepidemiology; 2004; 23(6):275-80. PubMed ID: 15297793
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Ataxia-oculomotor apraxia syndrome.
    Gascon GG; Abdo N; Sigut D; Hemidan A; Hannan MA
    J Child Neurol; 1995 Mar; 10(2):118-22. PubMed ID: 7782601
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DNA repair in trinucleotide repeat ataxias.
    Yau WY; O'Connor E; Sullivan R; Akijian L; Wood NW
    FEBS J; 2018 Oct; 285(19):3669-3682. PubMed ID: 30152109
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The genetics of movement disorders--spinocerebellar degenerations].
    Tallaksen CM; Dietrichs E
    Tidsskr Nor Laegeforen; 2004 Sep; 124(17):2233-5. PubMed ID: 15356686
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical and genetic aspects of spinocerebellar degeneration.
    Durr A; Brice A
    Curr Opin Neurol; 2000 Aug; 13(4):407-13. PubMed ID: 10970057
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia.
    Lorenzetti D; Bohlega S; Zoghbi HY
    Neurology; 1997 Oct; 49(4):1009-13. PubMed ID: 9339681
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study.
    Coutinho P; Ruano L; Loureiro JL; Cruz VT; Barros J; Tuna A; Barbot C; Guimarães J; Alonso I; Silveira I; Sequeiros J; Marques Neves J; Serrano P; Silva MC
    JAMA Neurol; 2013 Jun; 70(6):746-55. PubMed ID: 23609960
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J; Dalton A; Morrison PJ; Dodge A; Connarty M; Kotze MJ; Rubinsztein DC
    J Med Genet; 1997 Dec; 34(12):982-5. PubMed ID: 9429138
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical aspects of hereditary ataxias.
    Subramony SH
    J Child Neurol; 1995 Sep; 10(5):353-62. PubMed ID: 7499754
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes.
    Garces P; Antoniades CA; Sobanska A; Kovacs N; Ying SH; Gupta AS; Perlman S; Szmulewicz DJ; Pane C; Németh AH; Jardim LB; Coarelli G; Dankova M; Traschütz A; Tarnutzer AA
    Cerebellum; 2024 Feb; 23(1):121-135. PubMed ID: 36640220
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.
    Ranum LP; Lundgren JK; Schut LJ; Ahrens MJ; Perlman S; Aita J; Bird TD; Gomez C; Orr HT
    Am J Hum Genet; 1995 Sep; 57(3):603-8. PubMed ID: 7668288
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
    Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia.
    Bohlega SA; Shinwari JM; Al Sharif LJ; Khalil DS; Alkhairallah TS; Al Tassan NA
    BMC Med Genet; 2011 Feb; 12():27. PubMed ID: 21324166
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
    Ruano L; Melo C; Silva MC; Coutinho P
    Neuroepidemiology; 2014; 42(3):174-83. PubMed ID: 24603320
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.