BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 4980118)

  • 21. [Spinal cerebellar degeneration with propioceptive predominance; late appearance in a family].
    Poch GF; Martín AJ; Mariyos M; Rivero C
    Prensa Med Argent; 1969 Aug; 56(26):1299-301. PubMed ID: 5360961
    [No Abstract]   [Full Text] [Related]  

  • 22. [Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].
    Ben Hamida M; Chaabouni H; Madani S; Boussen S; Samoud S; Letaief F; Mrabet A; Hentati F; Miladi N
    J Genet Hum; 1986 Aug; 34(3-4):267-74. PubMed ID: 3760830
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Familial progressive myoclonus epilepsy (Unverricht/Lundborg)].
    Herbst A
    Psychiatr Neurol Med Psychol Beih; 1967; 6():18-39. PubMed ID: 5006319
    [No Abstract]   [Full Text] [Related]  

  • 24. Spino-pontine degeneration.
    Boller F; Segarra JM
    Eur Neurol; 1969; 2(6):356-73. PubMed ID: 5808476
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. Human epilepsy, episodic ataxia type 2, and migraine.
    Holtmann M; Opp J; Tokarzewski M; Korn-Merker E
    Lancet; 2002 Jan; 359(9301):170-1. PubMed ID: 11809294
    [No Abstract]   [Full Text] [Related]  

  • 27. [Neurodegenerative diseases of the spinal cord].
    Salachas F; Meininger V
    Rev Prat; 2001 Jun; 51(11):1197-201. PubMed ID: 11503489
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Hereditary degenerative spinocerebellar syndrome with extrapyramidal symptoms].
    Consoloni E; Rossi R; Ioppoli C; Cartei MA; Fonte F
    Riv Neurol; 1980; 50(4):221-30. PubMed ID: 7466218
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].
    Brion S; De Recondo J
    Rev Neurol (Paris); 1967 May; 116(5):383-400. PubMed ID: 6052813
    [No Abstract]   [Full Text] [Related]  

  • 30. [Clinical observations on 2 cases of hereditary areflexic dystasia].
    Fabiani F
    Riv Neurobiol; 1965; 11(2):219-27. PubMed ID: 5837065
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. A case of familial spinocerebellar degeneration with hypobetalipoproteinemia.
    Korula J; Namasivayam RK; Shadangi TN; Reddy PK; Raman PT
    Neurol India; 1976 Mar; 24(1):41-5. PubMed ID: 179026
    [No Abstract]   [Full Text] [Related]  

  • 33. Hereditary disease of the cerebellar parenchyma.
    Weiner LP; Konigsmark BW
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):192-6. PubMed ID: 5173359
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Heredity and generalized epilepsy.
    Vercelletto P; Courjon J
    Epilepsia; 1969 Mar; 10(1):7-21. PubMed ID: 4976753
    [No Abstract]   [Full Text] [Related]  

  • 35. [2 families in the Himeji area with spinocerebellar degeneration with primary symptoms of divergence paralysis].
    Itoga E; Kito S; Yamamoto M; Uchida Y
    Rinsho Shinkeigaku; 1975 Apr; 15(4):212-7. PubMed ID: 1170060
    [No Abstract]   [Full Text] [Related]  

  • 36. Hereditary degeneration of the optic nerve (hereditary optic atrophy).
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):999-1054. PubMed ID: 4907160
    [No Abstract]   [Full Text] [Related]  

  • 37. [Anatomical & clinical data on epilepsy. III. Spino-cerebellar degeneration with involuntary unilateral movements of athetosic type in an epileptic mental defective].
    COLLE G
    Acta Neurol Psychiatr Belg; 1958 Feb; 58(2):114-23. PubMed ID: 13532576
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Genetic generalized epilepsy. A follow-up study of 4 patients born between 1880-1892.
    Beaumanoir A; Martin F; Souza D
    Epilepsia; 1969 Mar; 10(1):69-75. PubMed ID: 4976751
    [No Abstract]   [Full Text] [Related]  

  • 40. [On a case of spino-cerebellar heredo-degeneration. (Roussy-Levy disease?)].
    Kohler C; Hermier M
    Rev Otoneuroophtalmol; 1966; 38(1):58-64. PubMed ID: 5931801
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.