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 *

118 related articles for article (PubMed ID: 6681562)

  • 1. Joseph disease in a non-Portuguese family.
    Sakai T; Ohta M; Ishino H
    Neurology; 1983 Jan; 33(1):74-80. PubMed ID: 6681562
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Joseph disease: a multisystem degenerative disorder of the nervous system.
    Sachdev HS; Forno LS; Kane CA
    Neurology; 1982 Feb; 32(2):192-5. PubMed ID: 7198744
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dentatorubropallidoluysian degeneration: clinical, neuro-ophthalmologic, biochemical, and pathologic studies on autosomal dominant form.
    Goto I; Tobimatsu S; Ohta M; Hosokawa S; Shibasaki H; Kuroiwa Y
    Neurology; 1982 Dec; 32(12):1395-9. PubMed ID: 6890648
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions.
    Coutinho P; Andrade C
    Neurology; 1978 Jul; 28(7):703-9. PubMed ID: 566869
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Transmission of a neurologic degeneration in a family for 4 generations manifested under variable semiologic aspects (pure pyramidal, pure cerebello-pyramidal involvement or involvement with abolition of reflexes and severe sensory disorders].
    Mettey R; Hoppeler A; Gil R
    J Genet Hum; 1981 Sep; 29(3):227-34. PubMed ID: 7334346
    [No Abstract]   [Full Text] [Related]  

  • 6. Joseph disease in India--report of two families.
    Jain S; Maheshwari MC
    J Neurogenet; 1986 Jan; 3(1):61-73. PubMed ID: 3958821
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K; Kogure T; Oda T; Kato Y; Ohtani K; Endo K; Kosaka K; Amano N; Yagishita S
    No To Shinkei; 1993 Mar; 45(3):246-54. PubMed ID: 8323819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Myoclonus, cerebellar disorder, neuropathy, mitochondrial myopathy, and ACTH deficiency.
    Sasaki H; Kuzuhara S; Kanazawa I; Nakanishi T; Ogata T
    Neurology; 1983 Oct; 33(10):1288-93. PubMed ID: 6310438
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Autopsy cases of hereditary ataxia pathologically diagnosed as the Japanese type of Joseph disease--cliniconeuropathological findings].
    Kogure T; Oda T; Katoh Y
    Seishin Shinkeigaku Zasshi; 1990; 92(3):161-83. PubMed ID: 2353076
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity.
    Woods BT; Schaumburg HH
    J Neurol Sci; 1972 Oct; 17(2):149-66. PubMed ID: 5053922
    [No Abstract]   [Full Text] [Related]  

  • 11. Behr's syndrome. A family exhibiting pseudodominant inheritance.
    Thomas PK; Workman JM; Thage O
    J Neurol Sci; 1984 May; 64(2):137-48. PubMed ID: 6747661
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal recessive spino-olivo-cerebellar degeneration without ataxia.
    Staal A; Stefanko SZ; Jennekens FG; Vries-Bos LH; van Gijn J
    J Neurol Neurosurg Psychiatry; 1983 Jul; 46(7):648-52. PubMed ID: 6886703
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spinocerebellar degeneration with parkinsonian features: a clinical and pathological report.
    Weir RL; Fan KJ
    Ann Neurol; 1981 Jan; 9(1):87-9. PubMed ID: 7212673
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal inheritance in a family with mitochondrial encephalomyopathy.
    Torbergsen T; Borud O; Mathiesen E; Lindal S; Gustavson KH
    Prog Clin Biol Res; 1989; 306():129-33. PubMed ID: 2662209
    [No Abstract]   [Full Text] [Related]  

  • 15. [An autopsied case of alcoholic cerebellar degeneration with spastic paraplegia and neuropathy].
    Iwabuchi K; Yagishita S; Itoh Y; Amano N; Saitoh A
    No To Shinkei; 1990 May; 42(5):489-96. PubMed ID: 2169787
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A spinocerebellar degeneration with X-linked inheritance.
    Spira PJ; McLeod JG; Evans WA
    Brain; 1979 Mar; 102(1):27-41. PubMed ID: 427531
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heredo - familial spinocerebellar degeneration with slow eye movements--another variety of olivopontocerebellar degeneration.
    Wadia NH
    Neurol India; 1977 Sep; 25(3):147-60. PubMed ID: 613260
    [No Abstract]   [Full Text] [Related]  

  • 18. Hereditary cerebellar cortical and extrapyramidal nuclear abiotrophy in Kerry Blue Terriers.
    deLahunta A; Averill DR
    J Am Vet Med Assoc; 1976 Jun; 168(12):1119-24. PubMed ID: 931776
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Werdnig-Hoffmann disease].
    Perentes E; Donati F
    Rev Med Suisse Romande; 1981 Sep; 101(9):685-96. PubMed ID: 7302452
    [No Abstract]   [Full Text] [Related]  

  • 20. [Amyotrophic leukospongiosis (Miotch's disease)].
    Votiakov VI; Protas II; Nedz'ved' MK; Antonov IP; Prilutskaia AF
    Vestn Akad Med Nauk SSSR; 1975; (12):7-12. PubMed ID: 1227092
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.