BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 7499754)

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

  • 2. Degenerative ataxias.
    Subramony SH
    Curr Opin Neurol; 1994 Aug; 7(4):316-22. PubMed ID: 7952239
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic diagnosis, classification and clinical hereditary ataxia disease entities].
    Schöls L; Riess O; Amoiridis G; Riess A; Przuntek H; Epplen JT
    Fortschr Neurol Psychiatr; 1997 Feb; 65(2):79-89. PubMed ID: 9157050
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Classification and diagnosis of degenerative ataxias].
    Klockgether T; Bürk K; Auburger G; Dichgans J
    Nervenarzt; 1995 Aug; 66(8):571-81. PubMed ID: 7566268
    [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. Joubert syndrome.
    Solomon R; Jana AK; Singh S; Biswas A
    Indian Pediatr; 2001 Sep; 38(9):1045-9. PubMed ID: 11568384
    [No Abstract]   [Full Text] [Related]  

  • 7. Inherited ataxias.
    Harding AE
    Curr Opin Neurol; 1995 Aug; 8(4):306-9. PubMed ID: 7582047
    [No Abstract]   [Full Text] [Related]  

  • 8. Hereditary ataxias: overview.
    Jayadev S; Bird TD
    Genet Med; 2013 Sep; 15(9):673-83. PubMed ID: 23538602
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Hereditary cerebellar ataxias: from hammer to genetics].
    Arruda WO; Teive HA
    Arq Neuropsiquiatr; 1997 Sep; 55(3B):666-76. PubMed ID: 9629425
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [At the crossroads between developmental and degenerative diseases: the cerebellar disorders of early infancy. Classification and practical approach].
    Landrieu P; Kamoun F
    Rev Neurol (Paris); 2003 Apr; 159(4):382-94. PubMed ID: 12773867
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pseudodominant inheritance of spastic ataxia of Charlevoix-Saguenay.
    Terracciano A; Foulds NC; Ditchfield A; Bunyan DJ; Crolla JA; Huang S; Santorelli FM; Hammans SR
    Neurology; 2010 Apr; 74(14):1152-4. PubMed ID: 20368637
    [No Abstract]   [Full Text] [Related]  

  • 12. Molecular genetics of hereditary ataxias.
    Banfi S; Zoghbi HY
    Baillieres Clin Neurol; 1994 Aug; 3(2):281-95. PubMed ID: 7952848
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The inherited ataxias.
    Stumpf DA
    Pediatr Neurol; 1985; 1(3):129-33. PubMed ID: 3916902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MR imaging of degenerative disorders of brainstem and cerebellum.
    Berciano J
    Magn Reson Imaging; 1991; 9(3):467. PubMed ID: 1881267
    [No Abstract]   [Full Text] [Related]  

  • 15. MR imaging of degenerative disorders of brainstem and cerebellum.
    Gallucci M; Splendiani A; Bozzao A; Baldassarre M; Zobel BB; Masciocchi C; Passariello R
    Magn Reson Imaging; 1990; 8(2):117-22. PubMed ID: 2338892
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of cranial meningocele associated with Joubert syndrome.
    Suzuki T; Hakozaki M; Kubo N; Kuroda K; Ogawa A
    Childs Nerv Syst; 1996 May; 12(5):280-2. PubMed ID: 8737806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The molecular genetic approach to the study of dominant spinocerebellar ataxias].
    Illarioshkin SN; Ovchinnikov IV; Ivanova-Smolenskaia IA; Vereshchagin NV; Markova ED; Miklina NI; Kliushnikov SA
    Zh Nevrol Psikhiatr Im S S Korsakova; 1996; 96(1):37-41. PubMed ID: 8677716
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary ataxia.
    Rosenberg RN; Grossman A
    Neurol Clin; 1989 Feb; 7(1):25-36. PubMed ID: 2564162
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.
    Rantamäki M; Krahe R; Paetau A; Cormand B; Mononen I; Udd B
    Neurology; 2001 Sep; 57(6):1043-9. PubMed ID: 11571332
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.
    Saigoh K; Mitsui J; Hirano M; Shioyama M; Samukawa M; Ichikawa Y; Goto J; Tsuji S; Kusunoki S
    Parkinsonism Relat Disord; 2015 Mar; 21(3):332-4. PubMed ID: 25595316
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.