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2. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I. Benomar A; Le Guern E; Dürr A; Ouhabi H; Stevanin G; Yahyaoui M; Chkili T; Agid Y; Brice A Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871 [TBL] [Abstract][Full Text] [Related]
3. [Sectorial pigmented retinopathy secondary to acquired syphilis]. Cristiani R Ann Ottalmol Clin Ocul; 1967 Oct; 93(10):1099-108. PubMed ID: 5605815 [No Abstract] [Full Text] [Related]
5. [Electroretinography and electroencephalography in spinocerebellar degenerations]. Stanescu B; Wawernia E Arch Ophtalmol Rev Gen Ophtalmol; 1973 Jan; 33(1):43-8. PubMed ID: 4267723 [No Abstract] [Full Text] [Related]
6. [Nosology of Von Graefe-Lindenov syndrome. Study of mental disorders in this genetic neurosensory disease]. Nehlil J Ann Med Psychol (Paris); 1981 Mar; 139(3):352-6. PubMed ID: 7325492 [No Abstract] [Full Text] [Related]
7. Genetic approach to the nosology of retinal disorders. Klein D Birth Defects Orig Artic Ser; 1971 Mar; 7(3):52-82. PubMed ID: 4950917 [TBL] [Abstract][Full Text] [Related]
8. [Retinal degeneration and ophthalmoplegia associated with hereditary cerebellar ataxia]. De Marco P Riv Patol Nerv Ment; 1968 Feb; 89(1):34-46. PubMed ID: 5760400 [No Abstract] [Full Text] [Related]
9. [Dynamic visual acuity and recognition of carriers of pathologic genes]. Vérin P; Yaccoubi M Bull Soc Ophtalmol Fr; 1970 Dec; 70(12):1248-53. PubMed ID: 5526399 [No Abstract] [Full Text] [Related]
10. The clinical incidence of myoclonus. Halliday AM Mod Trends Neurol; 1967; 4(0):69-105. PubMed ID: 4277685 [No Abstract] [Full Text] [Related]