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 *

128 related articles for article (PubMed ID: 99688)

  • 1. Familial chorea and myoclonus epilepsy.
    Takahata N; Ito K; Yoshimura Y; Nishihori K; Suzuki H
    Neurology; 1978 Sep; 28(9 Pt 1):913-9. PubMed ID: 99688
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Study on two autopsied cases of degenerative type of myoclonus epilepsy with choreo-athetoid movement: Proposal of hereditary dentate and pallidal system atrophy (author's transl)].
    Naito H; Tanaka M; Hirose Y; Oyanagi S
    Seishin Shinkeigaku Zasshi; 1977; 79(4):193-204. PubMed ID: 407584
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy.
    Naito H; Oyanagi S
    Neurology; 1982 Aug; 32(8):798-807. PubMed ID: 6808417
    [No Abstract]   [Full Text] [Related]  

  • 5. Progressive myoclonus epilepsy with focal brainstem degeneration and paternal inheritance. An autopsy report of 4 cases from 2 pedigrees.
    Moss TH; Stevens DL; Campbell MJ
    Clin Neuropathol; 1996; 15(2):106-12. PubMed ID: 8925594
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Dentatorubropallidoluysian atrophy (DRPLA): comparative pathological study on clinical groups classified into juvenile, early adult and late adult types].
    Takeda S; Takahashi H; Ikuta F
    No To Shinkei; 1992 Feb; 44(2):111-6. PubMed ID: 1567729
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary dentatorubro-pallidoluysian atrophy (DRPLA): clinical studies on 45 cases].
    Yuasa T
    Nihon Rinsho; 1993 Nov; 51(11):3016-23. PubMed ID: 8277585
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ataxia, chorea, seizures, and dementia. Pathologic features of a newly defined familial disorder.
    Farmer TW; Wingfield MS; Lynch SA; Vogel FS; Hulette C; Katchinoff B; Jacobson PL
    Arch Neurol; 1989 Jul; 46(7):774-9. PubMed ID: 2742549
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ramsay Hunt syndrome in dentatorubral-pallidoluysian atrophy.
    Suzuki S; Kamoshita S; Ninomura S
    Pediatr Neurol; 1985; 1(5):298-301. PubMed ID: 3880416
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FAME 3: a novel form of progressive myoclonus and epilepsy.
    Carr JA; van der Walt PE; Nakayama J; Fu YH; Corfield V; Brink P; Ptacek L
    Neurology; 2007 Apr; 68(17):1382-9. PubMed ID: 17452583
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical picture of DRPLA].
    Naito H
    No To Shinkei; 1995 Oct; 47(10):931-8. PubMed ID: 7577137
    [No Abstract]   [Full Text] [Related]  

  • 12. Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study.
    Iizuka R; Hirayama K; Maehara KA
    J Neurol Neurosurg Psychiatry; 1984 Dec; 47(12):1288-98. PubMed ID: 6512549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ramsay Hunt syndrome: progressive mental deterioration in association with unusual cerebral white matter change.
    Kobayashi K; Morikawa K; Fukutani Y; Miyazu K; Nakamura I; Yamaguchi N; Watanabe H
    Clin Neuropathol; 1994; 13(2):88-96. PubMed ID: 8205732
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [(Neurological CPC.55). A 60-year-old woman with progressive cerebellar ataxia, myoclonus, and dementia].
    Morikawa N; Mori H; Sumino S; Kodera M; Shirai T; Kondo T; Mizuno Y
    No To Shinkei; 1997 Jul; 49(7):663-71. PubMed ID: 9234257
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and clinical findings in a family with dentatorubral-pallidoluysian atrophy.
    Potter NT; Meyer MA; Zimmerman AW; Eisenstadt ML; Anderson IJ
    Ann Neurol; 1995 Feb; 37(2):273-7. PubMed ID: 7847869
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A case of juvenile Alzheimer's disease with various neurological features such as myoclonus, showing grumose degeneration in the dentate nucleus].
    Hattori H; Tanaka S; Kondoh H; Nishimura T; Hashimoto S
    Rinsho Shinkeigaku; 1990 Jun; 30(6):647-53. PubMed ID: 2225661
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A family of dentato-rubro-pallido-Luysian atrophy including cases with schizophrenic symptoms].
    Naito H; Ohama E; Nagai H; Wakabayashi M; Morita M; Ikuta F
    Seishin Shinkeigaku Zasshi; 1987; 89(2):144-58. PubMed ID: 3114779
    [No Abstract]   [Full Text] [Related]  

  • 18. [An unclassified case of degenerative disease of the central nervous system--with reference to "hereditary pallidal and dentate system atrophy (Oyanagi)" (author's transl)].
    Maeshiro H; Kato U; Nakamura S; Hosaki H; Matsuyama H
    Seishin Shinkeigaku Zasshi; 1980; 82(4):234-48. PubMed ID: 6780996
    [No Abstract]   [Full Text] [Related]  

  • 19. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
    Warner TT; Lennox GG; Janota I; Harding AE
    Mov Disord; 1994 May; 9(3):289-96. PubMed ID: 8041369
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MERRF: a clinicopathological study. Relationships between myoclonus epilepsies and mitochondrial myopathies.
    Fukuhara N
    Rev Neurol (Paris); 1991; 147(6-7):476-9. PubMed ID: 1962054
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.