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 *

72 related articles for article (PubMed ID: 5512192)

  • 1. [Electroretinographic and electroencephalographic study in Strumpell-Lorrain spastic paraplegia].
    Stanescu B; Climescu E; Wawernia E
    Bull Mem Soc Fr Ophtalmol; 1970; 83():442-9. PubMed ID: 5512192
    [No Abstract]   [Full Text] [Related]  

  • 2. [Electroretinoencephalographic changes in tapeto-retinal degeneration].
    Stănescu B; Wawernie E
    Stud Cercet Neurol; 1970; 15(5):297-309. PubMed ID: 5312810
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [Usefulness of ETO preparation in treatment of retinal degenerative changes caused by high-grade myopia in the aspect of electroretinographic investigations (author's transl)].
    Palacz O; Kozielec J
    Klin Oczna; 1977 Dec; 47(12):579-81. PubMed ID: 609266
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. [FAMILIAL SPASTIC PARAPLEGIA OF THE TYPE STRUMPELL-LORRAIN IN 3 SISTERS DAUGHTERS OF A CONSANGUINOUS MARRIAGE].
    GOMEZ MALARET S; LATUFF H; CHOMPREDEPENA L
    Arch Pediatr Urug; 1963 Nov; 34():673-8. PubMed ID: 14123546
    [No Abstract]   [Full Text] [Related]  

  • 7. Spastic paraplegia, epilepsy, and mental retardation in several members of a family: a novel genetic disorder.
    Gigli GL; Diomedi M; Bernardi G; Placidi F; Marciani MG; Calia E; Maschio MC; Neri G
    Am J Med Genet; 1993 Mar; 45(6):711-6. PubMed ID: 8456849
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electroretinographic and electroencephalographic changes in dystrophia myotonica Steinert.
    Stănescu B; Wawernia E
    Ophthalmologica; 1970; 160(3):157-66. PubMed ID: 5435370
    [No Abstract]   [Full Text] [Related]  

  • 9. [Strümpell-Lorrain's spastic paraplegia (primary lateral sclerosis, familial spastic paralysis, etc.)].
    González-Elipe J; Vilanova A; Rapado A; Fernández-Criado M; Perianes J
    Rev Clin Esp; 1970 Nov; 119(3):233-40. PubMed ID: 5495928
    [No Abstract]   [Full Text] [Related]  

  • 10. Use of sugammadex in Strumpell-Lorrain disease: a report of two cases.
    Franco-Hernández JA; Rodríguez LM; Ortiz de Landázuri PJ; Hernández AG
    Braz J Anesthesiol; 2013; 63(1):113-5. PubMed ID: 23438806
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and electroretinographic findings in a sodium fluoride long treated group of patients.
    Guerra R; Medaglini E
    Ann Ottalmol Clin Ocul; 1968 Apr; 94(4):327-33. PubMed ID: 5708187
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Familial spastic paraplegia and maculopathy with juxtafoveolar retinal telangiectasis and subretinal neovascularization.
    Leys A; Gilbert HD; Van De Sompel W; Verougstraete C; Devriendt K; Lagae L; Gass JD
    Retina; 2000; 20(2):184-9. PubMed ID: 10783952
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Electroretinographic control of the action of theophylline nicotinate on some vascular diseases of the retina].
    Cordella M; Vinciguerra E
    Ann Ottalmol Clin Ocul; 1967 Dec; 93(12):1267-80. PubMed ID: 5605983
    [No Abstract]   [Full Text] [Related]  

  • 15. Subarachnoid anesthesia for cesarean delivery in a parturient with Strümpell-Lorrain disease.
    Deruddre S; Marie M; Benhamou D
    Anesth Analg; 2006 Jun; 102(6):1910-1. PubMed ID: 16717359
    [No Abstract]   [Full Text] [Related]  

  • 16. [Secondary retinal degeneration].
    Fojutowa I; Smogulecka E
    Klin Oczna; 1973 Dec; 43(12):1369-72. PubMed ID: 4769384
    [No Abstract]   [Full Text] [Related]  

  • 17. [Strümpell-Lorrain disease and HLA typing. (A family report)].
    Blanckaert D; Gallet Y; Goudemand J; Dubois B; Morel P; Fontaine G
    Ann Pediatr (Paris); 1978 Sep; 25(7):345-7. PubMed ID: 16114345
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. The natural history of retinal degeneration in association with cobalamin C (cbl C) disease.
    Schimel AM; Mets MB
    Ophthalmic Genet; 2006 Mar; 27(1):9-14. PubMed ID: 16543196
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Retino-choroidal pigmented paravenous degeneration].
    Ardouin M; Beauchamp ; Chanteau Y; Urvoy M
    Bull Soc Ophtalmol Fr; 1967 Sep; 67(9):742-4. PubMed ID: 5622170
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.