BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 13297119)

  • 21. The global epidemiology of hereditary ataxia and spastic paraplegia: what are the messages?
    Braschinsky M
    Neuroepidemiology; 2014; 42(3):184-5. PubMed ID: 24603355
    [No Abstract]   [Full Text] [Related]  

  • 22. Fetal tissue grafts for cerebellar atrophy.
    Wu CY; Bao XF; Zhang C; Zhang QL
    Chin Med J (Engl); 1991 Mar; 104(3):198-203. PubMed ID: 2065529
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A refined evaluation of cerebellar ataxia and its application to treatment of spinocerebellar degeneration].
    Takayanagi T
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1297-9. PubMed ID: 8174329
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Brainstem auditory evoked responses in hereditary spinocerebellar ataxias.
    Knezevic W; Stewart-Wynne EG
    Clin Exp Neurol; 1985; 21():149-55. PubMed ID: 3870433
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].
    Kojima S
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1294-6. PubMed ID: 8174328
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cerebellar ataxia, congenital cataracts, and retarded somatic and mental maturation. Report of cases of Marinesco-Sjogren syndrome.
    ALTER M; TALBERT OR; CROFFEAD G
    Neurology; 1962 Dec; 12():836-47. PubMed ID: 14012309
    [No Abstract]   [Full Text] [Related]  

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

  • 28. Degenerative ataxic disorders: still perplexing.
    Harding A
    Br Med J (Clin Res Ed); 1987 Nov; 295(6608):1223-4. PubMed ID: 3120953
    [No Abstract]   [Full Text] [Related]  

  • 29. Late-onset cerebellar ataxia: Do not forget Friedreich's.
    Stamelou M
    Mov Disord; 2016 Jan; 31(1):7-8. PubMed ID: 26799250
    [No Abstract]   [Full Text] [Related]  

  • 30. Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
    Bürk K; Abele M; Fetter M; Dichgans J; Skalej M; Laccone F; Didierjean O; Brice A; Klockgether T
    Brain; 1996 Oct; 119 ( Pt 5)():1497-505. PubMed ID: 8931575
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Relationship between type 1 metabotropic glutamate receptors and cerebellar ataxia.
    Ishibashi K; Miura Y; Ishikawa K; Zhang MR; Toyohara J; Ishiwata K; Ishii K
    J Neurol; 2016 Nov; 263(11):2179-2187. PubMed ID: 27502082
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [The cerebellar cortical atrophy syndrome].
    Ponomareva EN; Astapenko AV; Likhachev SA; Ovsiankina GI; Pashko GV; Antonenko AI
    Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(9):14-9. PubMed ID: 9410595
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [CHRONIC PROGRESSIVE CEREBELLAR ATAXIA WITH TELANGIECTASIS (LOUIS-BAR SYNDROME). 1ST CASE IN SWITZERLAND].
    JUNGO O; GLAUSER P; KOENG E
    Helv Paediatr Acta; 1963 Nov; 18():280-305. PubMed ID: 14100862
    [No Abstract]   [Full Text] [Related]  

  • 34. Degree of cerebellar ataxia correlates with three-dimensional mri-based cerebellar volume in pure cerebellar degeneration.
    Richter S; Dimitrova A; Maschke M; Gizewski E; Beck A; Aurich V; Timmann D
    Eur Neurol; 2005; 54(1):23-7. PubMed ID: 16088175
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CANVAS: A very late onset cerebellar ataxia, due to biallelic expansions in the RFC1 gene.
    Tranchant C; Anheim M
    Rev Neurol (Paris); 2019 Oct; 175(9):493-494. PubMed ID: 31526553
    [No Abstract]   [Full Text] [Related]  

  • 36. 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]  

  • 37. Toward understanding polyglutamine-induced neurological disease in spinocerebellar ataxia type 1.
    Orr HT; Zoghbi HY
    Cold Spring Harb Symp Quant Biol; 1996; 61():649-57. PubMed ID: 9246491
    [No Abstract]   [Full Text] [Related]  

  • 38. [Olivopontocerebellar atrophy as an important differential diagnosis in atactic gait disorders in elderly patients].
    Waespe W; Hayek J; Wichmann W; Bader JP
    Schweiz Med Wochenschr; 1988 Jul; 118(27-28):1032-8. PubMed ID: 3166204
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Computerized tomography in the study of degenerative ataxia].
    De Michele G; Filla A; Mansi E; Delehaye L; Cirillo S; Di Geronimo G; Geri G; Campanella G
    Riv Neurol; 1987; 57(6):323-7. PubMed ID: 3330622
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hereditary disorders of the nervous system from anatomo-clinical studies to molecular biology.
    Martin JJ
    Acta Neurol Belg; 1996 Sep; 96(3):240-6. PubMed ID: 8886111
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.