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Quoted phrase not found in phrase index: "Familial dyskinesia and facial myokymia"
Page 1
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21.
Raskind WH, Matsushita M, Peter B, Biberston J, Wolff J, Lipe H, Burbank R, Bird TD. Raskind WH, et al. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):570-4. doi: 10.1002/ajmg.b.30879. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18980218 Free PMC article.
We previously reported a five-generation family manifesting an autosomal dominant disorder of facial myokymia and dystonic/choreic movements (FDFM). ...GENEHUNTER-MODSCORE Version 2.0.1 provided a maximum multipoint LOD score of 3.099. No other disorders prim …
We previously reported a five-generation family manifesting an autosomal dominant disorder of facial myokymia and dysto …
The neurology and natural history of patients with indeterminate CAG repeat length mutations of the Huntington disease gene.
Panegyres PK, Goh JG. Panegyres PK, et al. J Neurol Sci. 2011 Feb 15;301(1-2):14-20. doi: 10.1016/j.jns.2010.11.015. Epub 2010 Dec 13. J Neurol Sci. 2011. PMID: 21147489
Data from clinical histories, neurological examinations, the United Huntington's Disease Rating Scale (UHDRS) and MRI imaging were collected. RESULTS: Four patients developed facial chorea, ataxia, impaired tongue protrusion, abnormal saccades and intermittent eye pursuits …
Data from clinical histories, neurological examinations, the United Huntington's Disease Rating Scale (UHDRS) and MRI imaging were collected …
Gabapentin for treatment of pain and tremor: a large case series.
Merren MD. Merren MD. South Med J. 1998 Aug;91(8):739-44. doi: 10.1097/00007611-199808000-00007. South Med J. 1998. PMID: 9715219 Clinical Trial.
The other conditions treated that showed some improvement were benign essential/familial tremor, restless legs syndrome, centrally mediated pain, and periodic nighttime leg movements. ...
The other conditions treated that showed some improvement were benign essential/familial tremor, restless legs syndrome, centrally me …
Case of infantile onset spinocerebellar ataxia type 5.
Jacob FD, Ho ES, Martinez-Ojeda M, Darras BT, Khwaja OS. Jacob FD, et al. J Child Neurol. 2013 Oct;28(10):1292-5. doi: 10.1177/0883073812454331. Epub 2012 Aug 21. J Child Neurol. 2013. PMID: 22914369
Spinocerebellar ataxia type 5, a dominant spinocerebellar ataxia associated with mutations involving beta-III spectrin (SPTBN2), has been described in 3 families. It typically consists of a slowly progressive spinocerebellar ataxia with onset in the third decade. The autho …
Spinocerebellar ataxia type 5, a dominant spinocerebellar ataxia associated with mutations involving beta-III spectrin (SPTBN2), has been de …
The relationship between trinucleotide repeat length and phenotypic variation in Machado-Joseph disease.
Matsumura R, Takayanagi T, Fujimoto Y, Murata K, Mano Y, Horikawa H, Chuma T. Matsumura R, et al. J Neurol Sci. 1996 Jul;139(1):52-7. J Neurol Sci. 1996. PMID: 8836972
Group 1 and group 2 had common features of spasticity, hyperreflexia, Babinski sign, bulging eyes, facial myokymia and extrapyramidal signs as well as cerebellar ataxia and ophthalmoplegia. ...DNA analysis for the MJD mutation was clearly useful for making an accura …
Group 1 and group 2 had common features of spasticity, hyperreflexia, Babinski sign, bulging eyes, facial myokymia and extrapy …