BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 13928365)

  • 21. [Spinocerebellar hereditary degeneration (SCHD) associated with the Klinefelter syndrome].
    INDEMINI M; AMMANN F
    Confin Neurol; 1963; 23():155-64. PubMed ID: 13956475
    [No Abstract]   [Full Text] [Related]  

  • 22. Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.
    Mondelli M; Rossi A; Scarpini C; Guazzi GC
    Electromyogr Clin Neurophysiol; 1995 Nov; 35(7):415-24. PubMed ID: 8549432
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Serum lipoprotein fatty acid profile in hereditary ataxias.
    Iorio L; De Michele G; Filla A; Di Martino L; Postiglione A; Patti L; Campanella G
    Can J Neurol Sci; 1993 Aug; 20(3):206-9. PubMed ID: 8221384
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An investigation of pyruvate metabolism in patients with cerebellar and spinocerebellar degeneration.
    Livingstone IR; Mastaglia FL; Pennington RJ
    J Neurol Sci; 1980 Oct; 48(1):123-32. PubMed ID: 6893466
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. [HEREDITARY ATAXIA WITH UNUSUALLY MARKED SPASTIC FACTORS, WITH SPECIAL REFERENCE TO ITS RELATION TO HEREDITARY SPASTIC SPINAL PARALYSIS].
    OGASAWARA N
    Seishin Shinkeigaku Zasshi; 1963 Sep; 65():763-77. PubMed ID: 14134235
    [No Abstract]   [Full Text] [Related]  

  • 27. [THE SYMPTOM OF THE "DIFFICULT SIDE GLANCE" IN HEREDODEGENERATIVE SPINOCEREBELLAR DISEASES].
    KREINDLER A; POILICI I; CRIGHEL E
    Nervenarzt; 1963 Nov; 34():504-6. PubMed ID: 14160730
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. Thiamine status in inherited degenerative ataxias.
    Pedraza OL; Botez MI
    J Neurol Neurosurg Psychiatry; 1992 Feb; 55(2):136-7. PubMed ID: 1538220
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Brain levels of thiamine and its phosphate esters in Friedreich's ataxia and spinocerebellar ataxia type 1.
    Bettendorff L; Mastrogiacomo F; LaMarche J; Dozić S; Kish SJ
    Mov Disord; 1996 Jul; 11(4):437-9. PubMed ID: 8813226
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular genetic diagnosis of Friedreich's ataxia in a pedigree with apparent autosomal dominant spinocerebellar degeneration.
    De Silva R; Petty R; Loudon M; Frew C; Cooke A; Davidson R
    J Neurol Neurosurg Psychiatry; 1999 Jan; 66(1):117-8. PubMed ID: 9886474
    [No Abstract]   [Full Text] [Related]  

  • 32. [A hereditary ataxia associated with hypoalbuminemia and hyperlipidemia--a variant form of Friedreich's disease or a new clinical entity?].
    Uekawa K; Yuasa T; Kawasaki S; Makibuchi T; Ideta T
    Rinsho Shinkeigaku; 1992 Oct; 32(10):1067-74. PubMed ID: 1297549
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1.
    Eder K; Kish SJ; Kirchgessner M; Ross BM
    Mov Disord; 1998 Sep; 13(5):813-9. PubMed ID: 9756151
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Cardiac changes in hereditary spinocerebellar degenerations].
    Illarioshkin SN; Borisenko VV; Ivanova-Smolenskaia IA
    Ter Arkh; 1990; 62(10):88-92. PubMed ID: 2084900
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Electrophysiological and pathological studies in spinocerebellar degenerations.
    McLeod JG; Morgan JA
    Proc Aust Assoc Neurol; 1976; 13():113-7. PubMed ID: 1028997
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [SYNDROME OF SPINO-CEREBELLAR DEGENERATION WITH OPTIC ATROPHY AND DISTAL AMYOTROPHY OF THE CHARCOT-MARIE-TOOTH TYPE IN A 4-YEAR-OLD CHILD].
    BERNARD R; MOUREN P; SOULAYROL R; PINSARD N
    Pediatrie; 1963; 18():816-21. PubMed ID: 14106624
    [No Abstract]   [Full Text] [Related]  

  • 38. Hereditary spastic ataxia with central retinal degeneration and vestibular impairment. A clinical report on a family.
    BERGSTEDT M; JOHANSSON S; MULLER R
    Neurology; 1962 Feb; 12():124-32. PubMed ID: 13867802
    [No Abstract]   [Full Text] [Related]  

  • 39. [MARINESCO-SJOGREN DISEASE].
    PETROSILLO O; STAROPOLI D
    Ann Ottalmol Clin Ocul; 1963 Nov; 89():885-96. PubMed ID: 14109546
    [No Abstract]   [Full Text] [Related]  

  • 40. Immunoreactive levels of alpha-ketoglutarate dehydrogenase subunits in Friedreich's ataxia and spinocerebellar ataxia type 1.
    Mastrogiacomo F; LaMarche J; Dozić S; Lindsay G; Bettendorff L; Robitaille Y; Schut L; Kish SJ
    Neurodegeneration; 1996 Mar; 5(1):27-33. PubMed ID: 8731379
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.