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Annals of Neurology|August 12, 2000
Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonismM Maruyama, T Ikeuchi, M Saito, et al.
European Neurology|January 1, 1997
Clinical features of familial diffuse Lewy body diseaseA Ishikawa, H Takahashi, H Tanaka, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|January 14, 2003
Comparison of yeast-based estrogen receptor assaysM Saito, H Tanaka, A Takahashi, et al.
Neurology|May 1, 1991
Linkage analysis of juvenile parkinsonism to tyrosine hydroxylase gene locus on chromosome 11H Tanaka, A Ishikawa, E I Ginns, et al.
Biochemical and Biophysical Research Communications|July 17, 1995
Direct detection of expanded (CAG/CTG) repeats in the myotonin-protein kinase genes of myotonic dystrophy patients using a high-stringency hybridization methodK Sanpei, S Igarashi, I Eguchi, et al.
Seminars in Cell Biology|February 1, 1995
Dentatorubral-pallidoluysian atrophy (DRPLA): close correlation of CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipationT Ikeuchi, O Onodera, M Oyake, et al.
No to Shinkei = Brain and Nerve|October 1, 1996
[A case report of late-onset Huntington disease without family history and caudate atrophy who has diagnosed clinicopathologically and genetically]M Saito, A Ishikawa, K Iwanaga, et al.
Annals of Neurology|April 1, 1997
Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9T Ikeuchi, T Asaka, M Saito, et al.
The Japanese Journal of Experimental Medicine|October 1, 1978
Evaluation of the intrathoracic injection method for screening of filaricidesT Shibuya, H Tanaka, S Nogami, et al.
Neurology|January 27, 1998
Sporadic cases of dentatorubral-pallidoluysian atrophy associated with maternal transmissionT Shimohata, H Ishiguro, K Makino, et al.
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