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Annals of Neurology|March 1, 1995
The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14qH Tanaka, K Endo, S Tsuji, et al.Gastroenterology|July 1, 1987
Quantitative aspects of portal-systemic and arteriovenous shunts within the liver in cirrhosisK Ohnishi, N Chin, S Sugita, et al.Genomics|June 1, 1997
Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy geneS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.Human Genetics|April 1, 1997
Molecular genetic evidence of clinical heterogeneity in Fukuyama-type congenital muscular dystrophyE Kondo-Iida, K Saito, H Tanaka, et al.Annals of Neurology|July 1, 1996
X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome XqS N Illarioshkin, H Tanaka, E D Markova, et al.Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|September 1, 1996
Epithelial-myoepithelial carcinoma of the palateK Kusama, M Saito, M Kozu, et al.The American Journal of Gastroenterology|January 1, 1987
Effects of esophageal transection combined with splenectomy on portal hemodynamicsM Saito, K Ohnishi, H Tanaka, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 16, 1999
Nocturnal decrease in vasopressin secretion into plasma in patients with multiple system atrophyT Ozawa, H Tanaka, R Nakano, et al.Neuroscience Letters|August 18, 1995
GTP cyclohydrolase I gene in hereditary progressive dystonia with marked diurnal fluctuationH Ichinose, T Ohye, M Segawa, et al.Biochemical and Biophysical Research Communications|December 15, 1993
Chromosomal localization of the epsilon 1, epsilon 3 and zeta 1 subunit genes of the human NMDA receptor channelH Takano, O Onodera, H Tanaka, et al.Pageof 737