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Life Sciences|May 4, 2000
Reduced interleukin-1 responsiveness in immune system and central nervous system of inbred polydipsic (STR/N) miceK Okada, Y Yoshida, T Sugiura, et al.Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLAT Ikeuchi, R Koide, O Onodera, et al.Journal of the Neurological Sciences|May 23, 1998
Suprachiasmatic nucleus in a patient with multiple system atrophy with abnormal circadian rhythm of arginine-vasopressin secretion into plasmaT Ozawa, K Oyanagi, H Tanaka, et al.Archives of Neurology|June 16, 1999
Familial paroxysmal dystonic choreoathetosis: clinical findings in a large Japanese family and genetic linkage to 2qH Matsuo, K Kamakura, M Saito, et al.Human Molecular Genetics|June 1, 1996
A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness geneY Tamagawa, K Kitamura, T Ishida, et al.Brain & Development|September 14, 2000
Autosomal recessive juvenile parkinsonismM Saito, M Maruyama, K Ikeuchi, et al.The American Journal of Gastroenterology|October 1, 1987
Measurement of intrahepatic pressure as an index of hepatic sinusoidal pressureM Saito, K Ohnishi, H Terabayashi, et al.The American Journal of Gastroenterology|January 1, 1986
Clinical utility of pulsed Doppler flowmetry in patients with portal hypertensionK Ohnishi, M Saito, S Sato, et al.Acta Neuropathologica|August 15, 1998
Autosomal dominant diffuse Lewy body diseaseK Wakabayashi, S Hayashi, A Ishikawa, et al.American Journal of Medical Genetics|December 18, 1995
Lack of association between dopamine D4 receptor gene and schizophreniaT Tanaka, S Igarashi, O Onodera, et al.Pageof 737