BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 12564312)

  • 1. [Optic neuropathy in Strumpell-Lorrain disease: presentation of a clinical case and literature review].
    Makhoul J; Cordonnier M; Van Nechel C
    Bull Soc Belge Ophtalmol; 2002; (286):9-14. PubMed ID: 12564312
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].
    Saito T; Nishioka M; Ogino M; Endo K; Kowa H
    Rinsho Shinkeigaku; 1993 May; 33(5):519-24. PubMed ID: 8365058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Strümpell Lorrain's familial spasmodic paraplegia. An anatomical and clinical review and report on a new case (author's transl)].
    Buge A; Escourolle R; Rancurel G; Gray F; Pertuiset BF
    Rev Neurol (Paris); 1979; 135(4):329-37. PubMed ID: 504864
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation.
    Miyama S; Arimoto K; Kimiya S; Tomi H
    Neuropediatrics; 2000 Aug; 31(4):214-7. PubMed ID: 11071149
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
    Adachi T; Imaoka K; Shirasawa A; Yamaguchi S; Kobayashi S
    Rinsho Shinkeigaku; 1998 Dec; 38(12):1037-41. PubMed ID: 10349345
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Optic nerve hypoplasia associated with pupillary light-near dissociation, spastic paraparesis and other non-ocular anomalies.
    Doro D; Rossetti A; Battistella PA; Fardin P; Moro F
    Ital J Neurol Sci; 1988 Oct; 9(5):509-13. PubMed ID: 3215752
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A case of Gerstmann-Sträussler-Scheinker syndrome (P102L) accompanied by optic atrophy].
    Sugai F; Nakamori M; Nakatsuji Y; Abe K; Sakoda S
    Rinsho Shinkeigaku; 2000 Sep; 40(9):926-8. PubMed ID: 11257791
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Two siblings with spastic paraplegia, optic atrophy and peripheral neuropathy].
    Joshita Y; Atsumi T; Miyatake T
    Rinsho Shinkeigaku; 1982 Oct; 22(10):901-8. PubMed ID: 6303658
    [No Abstract]   [Full Text] [Related]  

  • 9. [Etiology and pathogenesis of familial spastic paraplegia (Strümpell-Lorrain disease)].
    Michałowicz R; Ignatowicz R; Kmieć T; Jóźwiak S
    Pol Tyg Lek; 1984 Aug; 39(32):1083-6. PubMed ID: 6504736
    [No Abstract]   [Full Text] [Related]  

  • 10. Hereditary spastic paraplegia.
    Roşulescu E; Stănoiu C; Buteică E; Stănoiu B; Burada F; Zăvăleanu M
    Rom J Morphol Embryol; 2009; 50(2):299-303. PubMed ID: 19434327
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes.
    Macedo-Souza LI; Kok F; Santos S; Licinio L; Lezirovitz K; Cavaçana N; Bueno C; Amorim S; Pessoa A; Graciani Z; Ferreira A; Prazeres A; de Melo AN; Otto PA; Zatz M
    Ann Hum Genet; 2009 May; 73(Pt 3):382-7. PubMed ID: 19344448
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Leber's hereditary optic neuropathy with childhood onset.
    Barboni P; Savini G; Valentino ML; La Morgia C; Bellusci C; De Negri AM; Sadun F; Carta A; Carbonelli M; Sadun AA; Carelli V
    Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5303-9. PubMed ID: 17122117
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)].
    Roger J; Pellissier JF; Dravet C; Bureau-Paillas M; Arnoux M; Larrieu JL
    Rev Neurol (Paris); 1982; 138(3):187-200. PubMed ID: 6810437
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Leber's disease with spastic paraplegia and peripheral neuropathy. Case report with nerve biopsy study.
    Pagès M; Pagès AM
    Eur Neurol; 1983; 22(3):181-5. PubMed ID: 6305662
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Classical Strumpell-Lorrain disease in a father and congenital diplegia in his son].
    Christodorescu D
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1977; 22(3):235-8. PubMed ID: 303794
    [No Abstract]   [Full Text] [Related]  

  • 16. [Strumpell-Lorrain disease: single nosologic entity?].
    Bettinazzi G; Amato L; Arcara A; Scoppa F
    Acta Neurol (Napoli); 1986 Jun; 8(3):259-62. PubMed ID: 3739774
    [No Abstract]   [Full Text] [Related]  

  • 17. Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13.
    Macedo-Souza LI; Kok F; Santos S; Amorim SC; Starling A; Nishimura A; Lezirovitz K; Lino AM; Zatz M
    Ann Neurol; 2005 May; 57(5):730-7. PubMed ID: 15852396
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. 3-Methylglutaconic aciduria in "optic atrophy plus".
    Costeff H; Elpeleg O; Apter N; Divry P; Gadoth N
    Ann Neurol; 1993 Jan; 33(1):103-4. PubMed ID: 8494328
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Non-progressive paraparesis in children with congenital ligamentous laxity.
    Moreira A; Wilson J
    Neuropediatrics; 1992 Feb; 23(1):49-52. PubMed ID: 1565219
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.