These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 7158329)

  • 1. Neuroaxonal dystrophy in childhood. Report of two second cousins with Hallerworden-Spatz disease, and a case of Seitelberger's disease.
    Malmström-Groth AG; Kristensson K
    Acta Paediatr Scand; 1982 Nov; 71(6):1045-9. PubMed ID: 7158329
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adult onset Hallervorden-Spatz syndrome or Seitelberger's disease with late onset: variants of the same entity? A clinico-pathological study.
    Gaytan-Garcia S; Kaufmann JC; Young GB
    Clin Neuropathol; 1990; 9(3):136-42. PubMed ID: 2364593
    [TBL] [Abstract][Full Text] [Related]  

  • 3. "Hallervorden-Spatz syndrome--infantile neuroaxonal dystrophy" complex. Case report.
    Bresolin AU; Pascuzzi L; Melaragno Filho R; Fontana MH; Pecora R; Souza Dias JC
    Arq Neuropsiquiatr; 1988 Mar; 46(1):69-72. PubMed ID: 3408385
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neuroaxonal dystrophy (Seitelberger's disease) with late onset, protracted course and myoclonic epilepsy.
    Scheithauer BW; Forno LS; Dorfman LJ; Kane CA
    J Neurol Sci; 1978 Apr; 36(2):247-58. PubMed ID: 418153
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Infantile neuroaxonal dystrophy (Seitelberger's disease). A light and ultrastructural study.
    Yagishita S; Kimura S
    Acta Neuropathol; 1975; 31(3):191-200. PubMed ID: 1138528
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease).
    Liu HM; Larson M; Mizuno Y
    Acta Neuropathol; 1974 Mar; 27(3):201-13. PubMed ID: 4842105
    [No Abstract]   [Full Text] [Related]  

  • 7. [Generalized infantile neuroaxonal dystrophies with pigmentation and lipophanerosis of the pallidum in concordant twins (author's transl)].
    Peiffer J; Brunner N; Landolt RF; Müller G; Schlote W
    Neuropadiatrie; 1976 Aug; 7(3):327-50. PubMed ID: 183173
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Infantile neuroaxonal dystrophy (Seitelberger's disease).
    Gordon N
    Dev Med Child Neurol; 2002 Dec; 44(12):849-51. PubMed ID: 12455862
    [No Abstract]   [Full Text] [Related]  

  • 9. [Infantile form of Hallervorden-Spatz disease (author's transl)].
    Marin L; Martin JJ; Ceuterick C
    Acta Neurol Belg; 1975; 75(6):257-66. PubMed ID: 1220521
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hallervorden-Spatz syndrome restricted to the pallidal nuclei.
    Kessler C; Schwechheimer K; Reuther R; Born JA
    J Neurol; 1984; 231(3):112-6. PubMed ID: 6481416
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Magnetic resonance tomography confirms the diagnosis of Hallervorden-Spatz disease].
    Scheer PJ; Perz A; Ebner F; Kratky-Dunitz M
    Padiatr Padol; 1988; 23(3):245-52. PubMed ID: 3186269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Juvenile spongious degeneration of the central nervous system. Its relation to Hallervorden-Spatz disease and the neuro-axonal dystrophies].
    Brucher JM; Dom R; Robin A
    Rev Neurol (Paris); 1968 Nov; 119(5):425-44. PubMed ID: 5715881
    [No Abstract]   [Full Text] [Related]  

  • 13. Late-onset Hallervorden-Spatz disease presenting as familial parkinsonism.
    Jankovic J; Kirkpatrick JB; Blomquist KA; Langlais PJ; Bird ED
    Neurology; 1985 Feb; 35(2):227-34. PubMed ID: 3969211
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and lewy body pathology.
    Wakabayashi K; Fukushima T; Koide R; Horikawa Y; Hasegawa M; Watanabe Y; Noda T; Eguchi I; Morita T; Yoshimoto M; Iwatsubo T; Takahashi H
    Acta Neuropathol; 2000 Mar; 99(3):331-6. PubMed ID: 10663979
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Magnetic resonance imaging in pathologically proven Hallervorden-Spatz disease.
    Schaffert DA; Johnsen SD; Johnson PC; Drayer BP
    Neurology; 1989 Mar; 39(3):440-2. PubMed ID: 2927660
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Seitelberger's connatal form of Pelizaeus-Merzbacher Disease. Case report, clinical, pathological and biochemical findings.
    Ulrich J; Herschkowitz N
    Acta Neuropathol; 1977 Oct; 40(2):129-36. PubMed ID: 201145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Hallervorden-Spatz disease with Lewy bodies].
    Antoine JC; Tommasi M; Chalumeau A; Jouvet-Telinge A; Bourrat C
    Rev Neurol (Paris); 1985; 141(12):806-9. PubMed ID: 3008295
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuropathological conditions related to neuroaxonal dystrophy.
    Seitelberger F
    Acta Neuropathol; 1971; 5():Suppl 5:17-29. PubMed ID: 5562689
    [No Abstract]   [Full Text] [Related]  

  • 19. Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations.
    Sethi KD; Adams RJ; Loring DW; el Gammal T
    Ann Neurol; 1988 Nov; 24(5):692-4. PubMed ID: 3202617
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome.
    Hayflick SJ; Penzien JM; Michl W; Sharif UM; Rosman NP; Wheeler PG
    Pediatr Neurol; 2001 Aug; 25(2):166-9. PubMed ID: 11551748
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.