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No to Hattatsu = Brain and Development|March 23, 2004
[Management of patients with Duchenne muscular dystrophy]Tadayuki IshiharaRinsho Shinkeigaku = Clinical Neurology|May 22, 2004
[Cardiopulmonary failure in Duchenne muscular dystrophy--pathophysiology and management]Tadayuki IshiharaThe International Journal of Biochemistry & Cell Biology|April 12, 2002
Increased expression level of the splicing variant of SIP1 in motor neuron diseasesWulin Aerbajinai, Tadayuki Ishihara, Kiichi Arahata, et al.Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 6, 2009
MELAS with diffuse degeneration of the cerebral white matter: report of an autopsy caseTeruo Yokoyama, Kazuko Hasegawa, Runko Obama, et al.Human Molecular Genetics|July 14, 2011
N88S seipin mutant transgenic mice develop features of seipinopathy/BSCL2-related motor neuron disease via endoplasmic reticulum stressTakuya Yagi, Daisuke Ito, Yoshihiro Nihei, et al.Rinsho Shinkeigaku = Clinical Neurology|April 20, 2006
[Long-term prognosis of the patients of myotonic dystrophy with tube feeding]Teruo Yokoyama, Michiko Takahasi, Ichiro Tsuchiya, et al.Disability and Rehabilitation|September 14, 2007
Dysphagia in patients with Duchenne muscular dystrophy evaluated with a questionnaire and videofluorographyKozo Hanayama, Meigen Liu, Yoshiko Higuchi, et al.Modern Rheumatology|December 18, 2008
Clinical and histopathological features of myopathies in Japanese patients with anti-SRP autoantibodiesTetsuya Takada, Michito Hirakata, Akira Suwa, et al.Journal of the Neurological Sciences|March 31, 2004
FSHD-like patients without 4q35 deletionGaku Yamanaka, Kanako Goto, Tadayuki Ishihara, et al.Internal Medicine (Tokyo, Japan)|December 7, 2007
Inflammatory myopathy with anti-Golgi antibody and anti-SS-A/Ro antibodyHidenori Hattori, Eiichiro Nagata, Tadayuki Ishihara, et al.Pageof 2