Search research articles
Contact Us
Filters
Showing results (41-50 of 98) with videos related to
Page
of 10
Sort By:
Journal of the Neurological Sciences
|
May 20, 1998
A small direct tandem duplication of the myelin protein zero gene in a patient with Dejerine-Sottas disease phenotype
N Tachi, N Kozuka, K Ohya, et al.
Journal of Intellectual Disability Research : JIDR
|
February 25, 1999
Long-term effects of zonisamide in the treatment of epilepsy in children with intellectual disability
K Iinuma, T Minami, K Cho, et al.
Pediatric Neurology
|
July 1, 1988
Walker-Warburg syndrome in a Japanese patient
N Tachi, M Tachi, K Sasaki, et al.
Pediatric Neurology
|
August 23, 2001
Fukuyama muscular dystrophy associated with lack of C-terminal domain of dystrophin
N Tachi, S Chiba, M Matsuo, et al.
Pediatric Neurology
|
April 1, 1995
Muscle involvement in congenital insensitivity to pain with anhidrosis
N Tachi, K Ohya, S Chiba, et al.
Journal of the Neurological Sciences
|
October 23, 1997
Congenital muscular dystrophy with partial deficiency of merosin
N Tachi, S Kamimura, K Ohya, et al.
Pediatric Neurology
|
May 30, 2001
A double mutation in a patient with X-linked myotubular myopathy
N Tachi, N Kozuka, S Chiba, et al.
Brain & Development
|
March 1, 1992
Demyelinating peripheral neuropathy in Cockayne syndrome: a histopathologic and morphometric study
K Sasaki, N Tachi, M Shinoda, et al.
Journal of the Neurological Sciences
|
June 1, 1994
Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III
N Tachi, K Kasai, S Chiba, et al.
Journal of the Neurological Sciences
|
July 1, 1992
Delayed expression of dystrophin on regenerating muscle from two siblings with Becker muscular dystrophy
N Tachi, S Wakai, Y Watanabe, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 98) with videos related to
Sort By:
Page
of 10
Journal of the Neurological Sciences
|
May 20, 1998
A small direct tandem duplication of the myelin protein zero gene in a patient with Dejerine-Sottas disease phenotype
N Tachi, N Kozuka, K Ohya, et al.
Journal of Intellectual Disability Research : JIDR
|
February 25, 1999
Long-term effects of zonisamide in the treatment of epilepsy in children with intellectual disability
K Iinuma, T Minami, K Cho, et al.
Pediatric Neurology
|
July 1, 1988
Walker-Warburg syndrome in a Japanese patient
N Tachi, M Tachi, K Sasaki, et al.
Pediatric Neurology
|
August 23, 2001
Fukuyama muscular dystrophy associated with lack of C-terminal domain of dystrophin
N Tachi, S Chiba, M Matsuo, et al.
Pediatric Neurology
|
April 1, 1995
Muscle involvement in congenital insensitivity to pain with anhidrosis
N Tachi, K Ohya, S Chiba, et al.
Journal of the Neurological Sciences
|
October 23, 1997
Congenital muscular dystrophy with partial deficiency of merosin
N Tachi, S Kamimura, K Ohya, et al.
Pediatric Neurology
|
May 30, 2001
A double mutation in a patient with X-linked myotubular myopathy
N Tachi, N Kozuka, S Chiba, et al.
Brain & Development
|
March 1, 1992
Demyelinating peripheral neuropathy in Cockayne syndrome: a histopathologic and morphometric study
K Sasaki, N Tachi, M Shinoda, et al.
Journal of the Neurological Sciences
|
June 1, 1994
Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III
N Tachi, K Kasai, S Chiba, et al.
Journal of the Neurological Sciences
|
July 1, 1992
Delayed expression of dystrophin on regenerating muscle from two siblings with Becker muscular dystrophy
N Tachi, S Wakai, Y Watanabe, et al.
Page
of 10