BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 36806180)

  • 1. [Gene Therapy for Ataxias].
    Klockgether T
    Fortschr Neurol Psychiatr; 2023 Apr; 91(4):147-152. PubMed ID: 36806180
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hereditary ataxias].
    Tallaksen CM
    Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1977-80. PubMed ID: 18787576
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parkinsonism & related disorders. Ataxias.
    Klockgether T
    Parkinsonism Relat Disord; 2007; 13 Suppl 3():S391-4. PubMed ID: 18267270
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI; Koenig M
    Handb Clin Neurol; 2013; 113():1869-78. PubMed ID: 23622410
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recent advances in degenerative ataxias.
    Klockgether T
    Curr Opin Neurol; 2000 Aug; 13(4):451-5. PubMed ID: 10970064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Distribution of dominant hereditary ataxias and Friedreich's ataxia in the Spanish population].
    Mayo Cabrero D; Hernández Cristóbal J; Cantarero Duque S; Martínez Delgado B; Urioste Azcorra M; Robledo Batanero M; García-Ruiz Espiga P; Benítez Ortiz J
    Med Clin (Barc); 2000 Jun; 115(4):121-5. PubMed ID: 10996881
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The inherited cerebellar ataxias: an update.
    Coarelli G; Wirth T; Tranchant C; Koenig M; Durr A; Anheim M
    J Neurol; 2023 Jan; 270(1):208-222. PubMed ID: 36152050
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia.
    Stefanescu MR; Dohnalek M; Maderwald S; Thürling M; Minnerop M; Beck A; Schlamann M; Diedrichsen J; Ladd ME; Timmann D
    Brain; 2015 May; 138(Pt 5):1182-97. PubMed ID: 25818870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quantification of circulating plasma DNA in Friedreich's ataxia and spinocerebellar ataxia types 2 and 12.
    Swarup V; Srivastava AK; Padma MV; Rajeswari MR
    DNA Cell Biol; 2011 Jun; 30(6):389-94. PubMed ID: 21329459
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.
    Gebus O; Montaut S; Monga B; Wirth T; Cheraud C; Alves Do Rego C; Zinchenko I; Carré G; Hamdaoui M; Hautecloque G; Nguyen-Them L; Lannes B; Chanson JB; Lagha-Boukbiza O; Fleury MC; Devys D; Nicolas G; Rudolf G; Bereau M; Mallaret M; Renaud M; Acquaviva C; Koenig M; Koob M; Kremer S; Namer IJ; Cazeneuve C; Echaniz-Laguna A; Tranchant C; Anheim M
    J Neurol; 2017 Jun; 264(6):1118-1126. PubMed ID: 28478596
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Ataxias. Diagnostic procedure and treatment].
    Klockgether T
    Nervenarzt; 2005 Oct; 76(10):1275-83; quiz 1284-5. PubMed ID: 16175415
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Degenerative and acquired sporadic adult onset ataxia.
    Lieto M; Roca A; Santorelli FM; Fico T; De Michele G; Bellofatto M; Saccà F; De Michele G; Filla A
    Neurol Sci; 2019 Jul; 40(7):1335-1342. PubMed ID: 30927137
    [TBL] [Abstract][Full Text] [Related]  

  • 14. EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
    van de Warrenburg BP; van Gaalen J; Boesch S; Burgunder JM; Dürr A; Giunti P; Klockgether T; Mariotti C; Pandolfo M; Riess O
    Eur J Neurol; 2014 Apr; 21(4):552-62. PubMed ID: 24418350
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The hereditary ataxias: Where are we now? Four decades of local research.
    Smith DC; Greenberg LJ; Bryer A
    S Afr Med J; 2016 May; 106(6 Suppl 1):S38-41. PubMed ID: 27245522
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Assessment of Ataxia Rating Scales and Cerebellar Functional Tests: Critique and Recommendations.
    Perez-Lloret S; van de Warrenburg B; Rossi M; Rodríguez-Blázquez C; Zesiewicz T; Saute JAM; Durr A; Nishizawa M; Martinez-Martin P; Stebbins GT; Schrag A; Skorvanek M;
    Mov Disord; 2021 Feb; 36(2):283-297. PubMed ID: 33022077
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. Current Status of Gene Therapy Research in Polyglutamine Spinocerebellar Ataxias.
    Afonso-Reis R; Afonso IT; Nóbrega C
    Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33921915
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Treatment for speech disorder in Friedreich ataxia and other hereditary ataxia syndromes.
    Vogel AP; Folker J; Poole ML
    Cochrane Database Syst Rev; 2014 Oct; (10):CD008953. PubMed ID: 25348587
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebellar ataxia in the eastern and southern parts of Norway.
    Koht J; Tallaksen CM
    Acta Neurol Scand Suppl; 2007; 187():76-9. PubMed ID: 17419835
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.