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T Miike

Showing results (31-40 of 107) with videos related to

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Brain & Development|January 1, 1997
Subacute sclerosing panencephalitis and chorioretinitisA Tomoda, T Miike, S Miyagawa, et al.
Brain & Development|July 1, 1991
Progressive myoclonus epilepsy: dentato-rubro-pallido-luysian atrophy (DRPLA) in childhoodA Tomoda, M Ikezawa, Y Ohtani, et al.
Clinical Genetics|February 1, 1991
XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardationT Matsumoto, K Taku, T Miike, et al.
No to Hattatsu = Brain and Development|January 1, 1990
[Two siblings with interstitial deletion of chromosome 14 [46 XX, del (14) (q12 q13.3)]]M Kodama, Y Kai, S Sugino, et al.
Brain & Development|January 1, 1989
Immunohistochemical dystrophin reaction in synaptic regionsT Miike, M Miyatake, J Zhao, et al.
Journal of the Neurological Sciences|December 1, 1987
Vascular endothelial cell injury and platelet embolism in Duchenne muscular dystrophy at the preclinical stageT Miike, S Sugino, Y Ohtani, et al.
Brain & Development|January 1, 1986
Muscle fiber type transformation in nemaline myopathy and congenital fiber type disproportionT Miike, Y Ohtani, H Tamari, et al.
The Journal of Pediatrics|August 10, 2000
Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failureN Iwatani, H Mabe, K Devriendt, et al.
Pediatric Neurology|February 22, 2001
Combined treatment with interferon-alpha and ribavirin for subacute sclerosing panencephalitisA Tomoda, S Shiraishi, M Hosoya, et al.
Human Mutation|March 27, 1999
Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. OnlineM Ikezawa, I Nishino, Y Goto, et al.
Pageof 11

Showing results (31-40 of 107) with videos related to

Sort By:
Pageof 11
Brain & Development|January 1, 1997
Subacute sclerosing panencephalitis and chorioretinitisA Tomoda, T Miike, S Miyagawa, et al.
Brain & Development|July 1, 1991
Progressive myoclonus epilepsy: dentato-rubro-pallido-luysian atrophy (DRPLA) in childhoodA Tomoda, M Ikezawa, Y Ohtani, et al.
Clinical Genetics|February 1, 1991
XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardationT Matsumoto, K Taku, T Miike, et al.
No to Hattatsu = Brain and Development|January 1, 1990
[Two siblings with interstitial deletion of chromosome 14 [46 XX, del (14) (q12 q13.3)]]M Kodama, Y Kai, S Sugino, et al.
Brain & Development|January 1, 1989
Immunohistochemical dystrophin reaction in synaptic regionsT Miike, M Miyatake, J Zhao, et al.
Journal of the Neurological Sciences|December 1, 1987
Vascular endothelial cell injury and platelet embolism in Duchenne muscular dystrophy at the preclinical stageT Miike, S Sugino, Y Ohtani, et al.
Brain & Development|January 1, 1986
Muscle fiber type transformation in nemaline myopathy and congenital fiber type disproportionT Miike, Y Ohtani, H Tamari, et al.
The Journal of Pediatrics|August 10, 2000
Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failureN Iwatani, H Mabe, K Devriendt, et al.
Pediatric Neurology|February 22, 2001
Combined treatment with interferon-alpha and ribavirin for subacute sclerosing panencephalitisA Tomoda, S Shiraishi, M Hosoya, et al.
Human Mutation|March 27, 1999
Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. OnlineM Ikezawa, I Nishino, Y Goto, et al.
Pageof 11