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T Ikeuchi

Showing results (281-290 of 303) with videos related to

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Neurology|June 27, 2008
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 familiesK Hara, A Shiga, H Nozaki, et al.
Journal of Medical Genetics|August 7, 2007
Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in AsiaN Maksimova, K Hara, A Miyashia, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|August 18, 2009
Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer diseaseK Kasuga, T Shimohata, A Nishimura, et al.
Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology|January 1, 1996
[Random biopsy and recurrence risk in patients with bladder cancer]Y Yamada, Y Hayashi, K Kohri, et al.
Annals of Neurology|December 24, 1997
Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese populationT Ikeuchi, H Takano, R Koide, et al.
Hinyokika Kiyo. Acta Urologica Japonica|September 30, 1998
[Clinical study on chlormadinone acetate alone followed by combination with LH-RH analogue for prostatic cancer: effects on lipid metabolism]M Shimada, H Uchida, T Kasahara, et al.
Neurology|February 13, 2002
Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorderP Hedera, S Rainier, X P Zhao, et al.
Genomics|October 29, 1998
Human genes for KNSL4 and MAZ are located close to one another on chromosome 16p11.2J Song, H Murakami, Z Q Yang, et al.
Translational Psychiatry|July 1, 2015
Genes associated with the progression of neurofibrillary tangles in Alzheimer's diseaseA Miyashita, H Hatsuta, M Kikuchi, et al.
Pageof 31

Showing results (281-290 of 303) with videos related to

Sort By:
Pageof 31
Neurology|June 27, 2008
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 familiesK Hara, A Shiga, H Nozaki, et al.
Journal of Medical Genetics|August 7, 2007
Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in AsiaN Maksimova, K Hara, A Miyashia, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|August 18, 2009
Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer diseaseK Kasuga, T Shimohata, A Nishimura, et al.
Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology|January 1, 1996
[Random biopsy and recurrence risk in patients with bladder cancer]Y Yamada, Y Hayashi, K Kohri, et al.
Annals of Neurology|December 24, 1997
Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese populationT Ikeuchi, H Takano, R Koide, et al.
Hinyokika Kiyo. Acta Urologica Japonica|September 30, 1998
[Clinical study on chlormadinone acetate alone followed by combination with LH-RH analogue for prostatic cancer: effects on lipid metabolism]M Shimada, H Uchida, T Kasahara, et al.
Neurology|February 13, 2002
Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorderP Hedera, S Rainier, X P Zhao, et al.
Genomics|October 29, 1998
Human genes for KNSL4 and MAZ are located close to one another on chromosome 16p11.2J Song, H Murakami, Z Q Yang, et al.
Translational Psychiatry|July 1, 2015
Genes associated with the progression of neurofibrillary tangles in Alzheimer's diseaseA Miyashita, H Hatsuta, M Kikuchi, et al.
Pageof 31