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 *

113 related articles for article (PubMed ID: 477009)

  • 1. Hallervorden-Spatz disease.
    Elejalde BR; de Elejalde MM; Lopez F
    Clin Genet; 1979 Jul; 16(1):1-18. PubMed ID: 477009
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hallervorden-Spatz disease].
    Ohno M; Goto I
    Nihon Rinsho; 1993 Nov; 51(11):2957-61. PubMed ID: 8277577
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hallervorden-Spatz disease: two new early childhood onset cases.
    Peña JA; Molina O; Cardozo J
    J Child Neurol; 2000 Jan; 15(1):30-2. PubMed ID: 10641607
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hallervorden-Spatz disease in twin patients].
    Makević M; Dordević D; Jovicić A; Umićević P; Mandić-Gajić G
    Vojnosanit Pregl; 1988; 45(4):305-7. PubMed ID: 3188415
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial pediatric rapidly progressive extrapyramidal syndrome: is it Hallervorden-Spatz disease?
    Chakravarty A; Mukherjee A; Sen A
    Pediatr Neurol; 2003 Aug; 29(2):170-2. PubMed ID: 14580665
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hallervorden-Spatz disease.
    Miller MB
    J Clin Psychiatry; 1989 Aug; 50(8):309. PubMed ID: 2760006
    [No Abstract]   [Full Text] [Related]  

  • 7. MR imaging in a case of Hallervorden-Spatz disease.
    Tanfani G; Mascalchi M; Dal Pozzo GC; Taverni N; Saia A; Trevisan C
    J Comput Assist Tomogr; 1987; 11(6):1057-8. PubMed ID: 3680689
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hallervorden-Spatz familial dystonia apropos of a family in which 3 brothers are afflicted. Diagnostic and genetic discussion].
    Cruz-Marin F; Gerard M; Brocard O; Gilgenkrantz S; Tridon P; Pierson M
    J Genet Hum; 1981 Sep; 29(3):253-8. PubMed ID: 7199561
    [No Abstract]   [Full Text] [Related]  

  • 9. Mineralization of the basal ganglia detected by CT in Hallervorden-Spatz syndrome.
    Tennison MB; Bouldin TW; Whaley RA
    Neurology; 1988 Jan; 38(1):154-5. PubMed ID: 3336450
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. [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]  

  • 12. 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]  

  • 13. [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]  

  • 14. Pigmentary degeneration of the retina in the Hallervorden-Spatz syndrome.
    Newell FW; Johnson RO; Huttenlocher PR
    Am J Ophthalmol; 1979 Sep; 88(3 Pt 1):467-71. PubMed ID: 573556
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hallervorden-Spatz disease with bilateral involvement of globus pallidus and substantia nigra: MR demonstration.
    Porter-Grenn L; Silbergleit R; Mehta BA
    J Comput Assist Tomogr; 1993; 17(6):961-3. PubMed ID: 8227584
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Early clinical and imaging (high-field MRI) diagnosis of Hallervorden-Spatz disease.
    Feliciani M; Curatolo P
    Neuroradiology; 1994 Apr; 36(3):247-8. PubMed ID: 8041454
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Late onset familial Hallervorden-Spatz disease: MR findings in two sisters.
    Ambrosetto P; Nonni R; Bacci A; Gobbi G
    AJNR Am J Neuroradiol; 1992; 13(1):394-6. PubMed ID: 1595483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hallervorden-Spatz disease: cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidus.
    Perry TL; Norman MG; Yong VW; Whiting S; Crichton JU; Hansen S; Kish SJ
    Ann Neurol; 1985 Oct; 18(4):482-9. PubMed ID: 4073841
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hallervorden Spatz syndrome (pantothenate kinase associated neurodegeneration) in two Sardinian brother with homozygous mutation in PANK 2 gene.
    Cossu G; Melis M; Floris G; Hayflick SJ; Spissu A
    J Neurol; 2002 Nov; 249(11):1599-600. PubMed ID: 12532925
    [No Abstract]   [Full Text] [Related]  

  • 20. Pathogenesis of pigment and spheroid formation in Hallervorden-Spatz syndrome and related disorders.
    Park BE; Netsky MG; Betsill WL
    Neurology; 1975 Dec; 25(12):1172-8. PubMed ID: 1238961
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.