BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 6472420)

  • 1. Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis.
    Eldridge R; Anayiotos CP; Schlesinger S; Cowen D; Bever C; Patronas N; McFarland H
    N Engl J Med; 1984 Oct; 311(15):948-53. PubMed ID: 6472420
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A Japanese family with probably autosomal dominant adult-onset leukodystrophy].
    Asahara H; Yoshimura T; Sada S; Furuya H; Kobayashi T
    Rinsho Shinkeigaku; 1996 Aug; 36(8):968-72. PubMed ID: 8958750
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and pathological features of an autosomal dominant, adult-onset leukodystrophy simulating chronic progressive multiple sclerosis.
    Schwankhaus JD; Katz DA; Eldridge R; Schlesinger S; McFarland H
    Arch Neurol; 1994 Aug; 51(8):757-66. PubMed ID: 8042923
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of simple form of sudanophilic leukodystrophy of a child which showed a marked loss of cerebral white matter and fatty liver].
    Hayashi K; Taguchi K; Tsutsumi A; Ogawa K; Fujita H; Hiramoto A; Taki T
    No To Shinkei; 1985 Oct; 37(10):957-63. PubMed ID: 4074573
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [CADASIL: 2 case reports of hereditary multi-infarct dementia].
    Otto V; Kaps M; Burgmann T; Kömpf D
    Fortschr Neurol Psychiatr; 1997 Feb; 65(2):90-5. PubMed ID: 9157051
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Cavitary orthochromatic leukodystrophy with oligodendroglial changes. A sporadic adult case].
    Graveleau P; Gray F; Plas J; Graveleau J; Brion S
    Rev Neurol (Paris); 1985; 141(11):713-8. PubMed ID: 4089401
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL.
    Hagel C; Groden C; Niemeyer R; Stavrou D; Colmant HJ
    Acta Neuropathol; 2004 Sep; 108(3):231-40. PubMed ID: 15221337
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Diagnostic criteria of borderline forms of multiple sclerosis].
    Dupel-Pottier C
    Rev Neurol (Paris); 2001 Sep; 157(8-9 Pt 2):935-43. PubMed ID: 11787358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MRI and CT in an autosomal-dominant, adult-onset leukodystrophy.
    Bergui M; Bradac GB; Leombruni S; Vaula G; Quattrocolo G
    Neuroradiology; 1997 Jun; 39(6):423-6. PubMed ID: 9225322
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nonspecific leukoencephalopathy associated with aging.
    Golomb J; Kluger A; Gianutsos J; Ferris SH; de Leon MJ; George AE
    Neuroimaging Clin N Am; 1995 Feb; 5(1):33-44. PubMed ID: 7743083
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cortical demyelination and diffuse white matter injury in multiple sclerosis.
    Kutzelnigg A; Lucchinetti CF; Stadelmann C; Brück W; Rauschka H; Bergmann M; Schmidbauer M; Parisi JE; Lassmann H
    Brain; 2005 Nov; 128(Pt 11):2705-12. PubMed ID: 16230320
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinically definite multiple sclerosis after radiological Schilder-like onset.
    Sastre-Garriga J; Rovira A; Río J; Tintoré M; Grivé E; Montalban X
    J Neurol; 2003 Jul; 250(7):871-3. PubMed ID: 12883933
    [No Abstract]   [Full Text] [Related]  

  • 13. [Leukodystrophies: clinical aspects and findings with computerized tomography and magnetic resonance imaging].
    Magnaldi S
    Radiol Med; 1991; 82(1-2):13-26. PubMed ID: 1896564
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hereditary dentatorubropallidoluysian atrophy--clinical variants in a family and degeneration of cerebral white matter in a proband].
    Miyashita K; Inuzuka T; Ishikawa A; Kondo H; Kawakami A; Takeda S; Ikuta F; Yuasa T
    No To Shinkei; 1992 Mar; 44(3):279-84. PubMed ID: 1591106
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary diffuse leucoencephalopathy with spheroids.
    Axelsson R; Röyttä M; Sourander P; Akesson HO; Andersen O
    Acta Psychiatr Scand Suppl; 1984; 314():1-65. PubMed ID: 6595937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Leukodystrophy in patients with ovarian dysgenesis.
    Schiffmann R; Tedeschi G; Kinkel RP; Trapp BD; Frank JA; Kaneski CR; Brady RO; Barton NW; Nelson L; Yanovski JA
    Ann Neurol; 1997 May; 41(5):654-61. PubMed ID: 9153528
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Alexander's disease in an adult].
    Habib M; Hassoun J; Ali-Cherif A; Alonzo B; Toga M; Khalil R
    Rev Neurol (Paris); 1984; 140(3):179-89. PubMed ID: 6729328
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Concentric sclerosis (Baló)].
    Tabira T
    Nihon Rinsho; 1994 Nov; 52(11):2971-5. PubMed ID: 7996696
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Adrenoleucodystrophy: a study of four patients.
    Procopis PG; Ouvrier RA
    Clin Exp Neurol; 1979; 16():133-8. PubMed ID: 575890
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Progressive neuronal degeneration of childhood: prenatal diagnosis by MRI.
    de Laveaucoupet J; Roffi F; Audibert F; Guis F; Lacroix C; Villeneuve N; Landrieu P; Labrune P
    Prenat Diagn; 2005 Apr; 25(4):307-10. PubMed ID: 15852481
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.