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8. Spinocerebellar ataxia associated with localized amyotrophy of the hands, sensorineural deafness and spastic paraparesis in two brothers. Gemignani F J Neurogenet; 1986 Mar; 3(2):125-33. PubMed ID: 3958822 [TBL] [Abstract][Full Text] [Related]
9. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy. McLeod JG; Low PA; Morgan JA Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391 [TBL] [Abstract][Full Text] [Related]
10. The autosomal dominant syndrome of progressive optic atrophy and congenital deafness. Kollarits CR; Pinheiro ML; Swann ER; Marcus DF; Corrie WS Am J Ophthalmol; 1979 Jun; 87(6):789-92. PubMed ID: 453309 [TBL] [Abstract][Full Text] [Related]
11. [Familial ataxia with peroneal muscular atrophy and optic atrophy]. Bernabo' Brea G; Rathschüler R; Rasore-Quartino A Riv Otoneurooftalmol; 1966; 41(4):273-90. PubMed ID: 5991731 [No Abstract] [Full Text] [Related]
12. [Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD syndrome) in 2 siblings]. Rybakowa M; Wisłocka E; Sołtysik-Wilk E; Pleti M; Bedkowska A Endokrynol Pol; 1983; 34(5):337-42. PubMed ID: 6671470 [No Abstract] [Full Text] [Related]
13. [Juvenile diabetes mellitus associated with optic nerve atrophy and neurogenic deafness. Description of 2 cases]. Della Porta G; De Ritis L Minerva Pediatr; 1977 Sep; 29(29):1799-801. PubMed ID: 927400 [No Abstract] [Full Text] [Related]
14. Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy. Melo TP; Ferro JM J Neurol Neurosurg Psychiatry; 1989 Dec; 52(12):1448-9. PubMed ID: 2614456 [No Abstract] [Full Text] [Related]
15. The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect. Bradley WG; Richardson J; Frew IJ Brain; 1974 Sep; 97(3):521-32. PubMed ID: 4213898 [No Abstract] [Full Text] [Related]
16. [Familial syndrome of diabetes mellitus, primary optic nerve atrophy and inner-ear deafness]. Sauer H; Chüden H; Gottesbüren H; Schmitz-Valckenberg P; Seitz D Dtsch Med Wochenschr; 1973 Feb; 98(6):243-55. PubMed ID: 4684648 [No Abstract] [Full Text] [Related]
17. Behr's syndrome: familial optic atrophy, spastic diplegia and ataxia. Landrigan PJ; Berenberg W; Bresnan M Dev Med Child Neurol; 1973 Feb; 15(1):41-7. PubMed ID: 4354046 [No Abstract] [Full Text] [Related]
18. HLA type and islet cell antibody status in family with (diabetes insipidus and mellitus, optic atrophy, and deafness) DIDMOAD syndrome. Monson JP; Boucher BJ Lancet; 1983 Jun; 1(8336):1286-7. PubMed ID: 6134087 [No Abstract] [Full Text] [Related]
19. [CHARCOT-MARIE AMYOTROPHY ASSOCIATED WITH A BILATERAL OPTIC ATROPHY]. SERRATRICE G; TATOSSIAN A; POINSO Y Presse Med (1893); 1964 Oct; 72():2535-6. PubMed ID: 14191631 [No Abstract] [Full Text] [Related]
20. A family with neurogenic atrophy of the distal muscles of the upper limbs: clinical and electrophysiological studies. Vignaendra V; Ghee T Med J Aust; 1976 Oct; 2(17):639-41. PubMed ID: 994976 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]