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Journal of Human Genetics
|
March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Mingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Internal Medicine (Tokyo, Japan)
|
February 2, 2013
Evaluation of the efficacy of pramipexole for treating levodopa-induced dyskinesia in patients with Parkinson's disease
Hiroya Utsumi, Yasuyuki Okuma, Osamu Kano, et al.
The Journal of Biological Chemistry
|
August 15, 2009
Depletion of vitamin E increases amyloid beta accumulation by decreasing its clearances from brain and blood in a mouse model of Alzheimer disease
Yoichiro Nishida, Shingo Ito, Sumio Ohtsuki, et al.
Journal of the Neurological Sciences
|
April 18, 2012
Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations
Madoka Mori-Yoshimura, Kazunari Monma, Naoki Suzuki, et al.
American Journal of Human Genetics
|
July 8, 2005
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains
Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, et al.
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of 4
Search research articles
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Showing results (31-40 of 35) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 35 results.
Journal of Human Genetics
|
March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Mingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Internal Medicine (Tokyo, Japan)
|
February 2, 2013
Evaluation of the efficacy of pramipexole for treating levodopa-induced dyskinesia in patients with Parkinson's disease
Hiroya Utsumi, Yasuyuki Okuma, Osamu Kano, et al.
The Journal of Biological Chemistry
|
August 15, 2009
Depletion of vitamin E increases amyloid beta accumulation by decreasing its clearances from brain and blood in a mouse model of Alzheimer disease
Yoichiro Nishida, Shingo Ito, Sumio Ohtsuki, et al.
Journal of the Neurological Sciences
|
April 18, 2012
Heterozygous UDP-GlcNAc 2-epimerase and N-acetylmannosamine kinase domain mutations in the GNE gene result in a less severe GNE myopathy phenotype compared to homozygous N-acetylmannosamine kinase domain mutations
Madoka Mori-Yoshimura, Kazunari Monma, Naoki Suzuki, et al.
American Journal of Human Genetics
|
July 8, 2005
An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains
Kinya Ishikawa, Shuta Toru, Taiji Tsunemi, et al.
Page
of 4