Square Wave Jerks and Other ENG Findings in a Patient with Hereditary Parkinson’s Disease (PARK 2)
Author:
Affiliation:
1. Department of Neurology, Juntendo University School of Medicine
2. Department of Neurology, Amakusa Rehabilitation Hospital
3. Department of Oto-Rhino-Laryngology, Juntendo University School of Medicine
Publisher
Japan Society of Equilibrium Research
Link
https://www.jstage.jst.go.jp/article/jser/83/1/83_23/_pdf
Reference51 articles.
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2. 2) Hattori N, Kitada T, Matsumine H, et al.: Molecular genetic analysis of a novel parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the parkin gene in affected individuals. Ann Neurol 44: 935–941, 1998
3. 3) Lohmann E, Periquet M, Bonifati V, et al.: How much phenotypic variation can be attributed to parkin genotype? Ann Neurol 54: 176–185, 2003
4. 4) Suzuki M, Hattori N, Orimo S, et al.: Preserved myocardial [123I] metaiodo-benzylguanidine uptake in autosomal recessive juvenile parkinsonism: First case report. Mov Disord 20: 634–636, 2005
5. 5) Ishikawa A, Tsuji S: Clinical analysis of 17 patients in 12 Japanese families with autosomal recessive type juvenile parkinsonism. Neurology 47: 160–166, 1996
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