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5. Compound mitochondrial DNA mutations in a neurological patient with ataxia, myoclonus and deafness. Park JH; Yoon BR; Kim HJ; Lee PH; Choi BO; Chung KW J Genet; 2014 Apr; 93(1):173-7. PubMed ID: 24840835 [No Abstract] [Full Text] [Related]
6. Progressive ataxia, palatal tremor, and the Romberg sign. Teive HA; Munhoz RP Arch Neurol; 2009 Feb; 66(2):284-5; author reply 285. PubMed ID: 19204175 [No Abstract] [Full Text] [Related]
14. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 27-1995. A 29-month-old girl with worsening ataxia, nystagmus, and subsequent opsoclonus and myoclonus. N Engl J Med; 1995 Aug; 333(9):579-86. PubMed ID: 7623909 [No Abstract] [Full Text] [Related]
15. [A 37-year-old woman with deafness, decrease of visual acuity, dysarthria, myoclonus and changes in eye movements of a 20-year evolution (clinicopathological conference)]. Illa I; Casademont J Med Clin (Barc); 1998 May; 110(16):630-7. PubMed ID: 9656202 [No Abstract] [Full Text] [Related]
16. [NARP syndrome--a less known mitochondrial disease]. Kuusisto H; Simola KO; Keränen T Duodecim; 2003; 119(16):1563-6. PubMed ID: 14535029 [No Abstract] [Full Text] [Related]
17. [Ataxia and deafness secondary to meningitis in children: the role of labyrinth diseases]. Landthaler G; Andrieu-Guitrancourt J Arch Fr Pediatr; 1975 Apr; 32(4):319-35. PubMed ID: 1164146 [TBL] [Abstract][Full Text] [Related]