BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

664 related articles for article (PubMed ID: 17112370)

  • 41. Hereditary ataxias: epidemiological aspects.
    Werdelin L; Keiding N
    Neuroepidemiology; 1990; 9(6):321-31. PubMed ID: 2096315
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Spinocerebellar ataxia, hypogonadotropic hypogonadism, and choroidal dystrophy (Boucher-Neuhäuser syndrome).
    Limber ER; Bresnick GH; Lebovitz RM; Appen RE; Gilbert-Barness EF; Pauli RM
    Am J Med Genet; 1989 Jul; 33(3):409-14. PubMed ID: 2801777
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism.
    Neuhäuser G; Opitz JM
    Clin Genet; 1975; 7(5):426-34. PubMed ID: 1149314
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Large-fiber sensory neuronopathy in autosomal dominant spinocerebellar degeneration.
    Bennett RH; Ludvigson P; DeLeon G; Berry G
    Arch Neurol; 1984 Feb; 41(2):175-8. PubMed ID: 6318705
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Sex-linked recessive congenital ataxia.
    Young ID; Moore JR; Tripp JH
    J Neurol Neurosurg Psychiatry; 1987 Sep; 50(9):1230-2. PubMed ID: 3668574
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Autosomal dominant pure cerebellar ataxia. Neurological and genetic study.
    Frontali M; Spadaro M; Giunti P; Bianco F; Jodice C; Persichetti F; Colazza GB; Lulli P; Terrenato L; Morocutti C
    Brain; 1992 Dec; 115 ( Pt 6)():1647-54. PubMed ID: 1486455
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The Development of a New Patient-Reported Outcome Measure in Recessive Ataxias: The Person-Reported Ataxia Impact Scale.
    Tremblay M; Brais B; Asselin V; Buffet M; Girard A; Girard D; Berbiche D; Gagnon C
    Cerebellum; 2024 Apr; 23(2):512-522. PubMed ID: 37165279
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Familial ataxia with abnormal CSF, with special reference to an autopsy case from three affected siblings.
    Nakamura I; Kurachi M; Fukutani Y; Kawasaki Y; Yamaguchi N; Torii H
    Jpn J Psychiatry Neurol; 1988 Jun; 42(2):277-89. PubMed ID: 2853803
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.
    Filla A; De Michele G; Cavalcanti F; Perretti A; Santoro L; Barbieri F; D'Arienzo G; Campanella G
    J Neurol Neurosurg Psychiatry; 1990 Aug; 53(8):667-70. PubMed ID: 2213043
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Neurochemical and genetic bases of psychopathology: future directions.
    Matthysse S; Kling M
    Behav Genet; 1982 Feb; 12(1):101-9. PubMed ID: 6124231
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Cerebellar ataxia of early onset: clinical symptoms and MRI findings].
    Yamashita S; Miyake S; Yamada M; Iwamoto H; Yamada K
    No To Hattatsu; 1989 Jul; 21(4):327-33. PubMed ID: 2789855
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Heredoataxia (spinocerebellar degeneration), ERG alterations, temporal aspects.
    Stanescu-Segal B; Michiels J
    Ophthalmologica; 1979; 178(5):267-72. PubMed ID: 492674
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.
    Mahdieh N; Heidari M; Rezaei Z; Tavasoli AR; Hosseinpour S; Rasulinejad M; Dehnavi AZ; Ghahvechi Akbari M; Badv RS; Vafaei E; Mohebbi A; Mohammadi P; Hosseiny SMM; Azizimalamiri R; Nikkhah A; Pourbakhtyaran E; Rohani M; Khanbanha N; Nikbakht S; Movahedinia M; Karimi P; Ghabeli H; Hosseini SA; Rashidi FS; Garshasbi M; Kashani MR; Ghiasvand NM; Zuchner S; Synofzik M; Ashrafi MR
    Hum Genomics; 2024 Apr; 18(1):35. PubMed ID: 38570878
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Familial paroxysmal ataxia: report of a family.
    Hawkes CH
    J Neurol Neurosurg Psychiatry; 1992 Mar; 55(3):212-3. PubMed ID: 1564484
    [TBL] [Abstract][Full Text] [Related]  

  • 55. R-loops in proliferating cells but not in the brain: implications for AOA2 and other autosomal recessive ataxias.
    Yeo AJ; Becherel OJ; Luff JE; Cullen JK; Wongsurawat T; Jenjaroenpun P; Kuznetsov VA; McKinnon PJ; Lavin MF
    PLoS One; 2014; 9(3):e90219. PubMed ID: 24637776
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias.
    Kaakkola S; Marnela KM; Oja SS; Icén A; Palo J
    Acta Neurol Scand; 1990 Oct; 82(4):225-9. PubMed ID: 2270751
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Thiamin contents of cerebrospinal fluid, plasma and erythrocytes in cerebellar ataxias.
    Poloni M; Mazzarello P; Laforenza U; Caramella C; Patrini C
    Eur Neurol; 1992; 32(3):154-8. PubMed ID: 1592072
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Dominantly inherited congenital cerebellar ataxia with atrophy of the vermis.
    Tomiwa K; Baraitser M; Wilson J
    Pediatr Neurol; 1987; 3(6):360-2. PubMed ID: 3334022
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family.
    Harding AE; Diengdoh JV; Lees AJ
    J Neurol Neurosurg Psychiatry; 1984 Aug; 47(8):853-6. PubMed ID: 6470726
    [TBL] [Abstract][Full Text] [Related]  

  • 60. X-linked recessive inheritance of ataxia and adult-onset dementia: clinical features and preliminary linkage analysis.
    Farlow MR; DeMyer W; Dlouhy SR; Hodes ME
    Neurology; 1987 Apr; 37(4):602-7. PubMed ID: 3470628
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 34.