- Dentatorubral–
pallidoluysian atrophy (DRPLA) is an
autosomal dominant spinocerebellar degeneration caused by an
expansion of a CAG
repeat encoding a polyglutamine...
- 1093/ageing/afp020. PMID 19276093. Tsuji, S. (1999). "Dentatorubral-
pallidoluysian atrophy:
Clinical features and
molecular genetics". Adv Neurol. 79:...
-
spinocerebellar ataxias type 1, 3 and 17, neuroacanthocytosis, dentatorubral-
pallidoluysian atrophy (DRPLA),
brain iron ac****ulation disorders, Wilson's disease...
-
dominant diseases that can be
misdiagnosed as HD are dentatorubral-
pallidoluysian atrophy and neuroferritinopathy. Also, some
autosomal recessive disorders...
-
disorder known as "dentatorubral-
pallidoluysian atrophy" or "dentatorubropallidoluysian atrophy". Dentatorubral-
pallidoluysian atrophy (DRPLA) is a rare neurodegenerative...
-
spinocerebellar ataxias type 1 and 3, neuroacanthocytosis, dentatorubral-
pallidoluysian atrophy (DRPLA),
brain iron ac****ulation disorders, Wilson's disease...
-
Huntington disease-like 2, spinal-bulbar
muscular atrophy, dentatorubral-
pallidoluysian atrophy, and
spinocerebellar ataxia 1–3, 6–8, and 17. The
first main...
-
protein has also been
identified as
interacting with the dentatorubral-
pallidoluysian atrophy gene,
which is ****ociated with an
autosomal dominant neurodegenerative...
- SCA34-SCA37,
autosomal dominant cerebellar ataxia and
dentatorubral pallidoluysian atrophy. Type I ADCA is
characterized by
different symptoms of ataxia...
-
improving neurological dysfunction in a
patient with dentatorubral-
pallidoluysian atrophy (DRPLA)".
Epilepsy Behav Case Rep. 8: 44–46. doi:10.1016/j.ebcr...
