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Journal of Human Genetics
|
June 8, 2001
Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant connexin 32 (GJB1)
W Matsuyama, M Nakagawa, T Moritoyo, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
September 1, 1987
[Quantification of plasminogen activator antigen in plasma by ELISA and age-related changes in its concentration]
M Soma, Y Maeda, M Ueda, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
March 23, 1999
Loss of 123I-MIBG uptake by the heart in Parkinson's disease: assessment of cardiac sympathetic denervation and diagnostic value
A Satoh, T Serita, M Seto, et al.
Experimental Neurology
|
December 1, 1993
Immortalized GABAergic cell lines derived from rat striatum using a temperature-sensitive allele of the SV40 large T antigen
M Giordano, H Takashima, A Herranz, et al.
Journal of the Neurological Sciences
|
March 27, 2001
Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence
M Nakagawa, H Takashima, F Umehara, et al.
Acta Neurologica Scandinavica
|
July 1, 1992
Systemic interferon-alpha in the treatment of HTLV-I-associated myelopathy
Y Kuroda, K Kurohara, F Fujiyama, et al.
Clinical Nuclear Medicine
|
August 26, 1998
False-positive iodine-131 whole-body imaging due to gestational sac
Y Nishiyama, Y Yamamoto, K Takahashi, et al.
Neuropediatrics
|
March 19, 2009
Genetically confirmed patients with merosin-deficient congenital muscular dystrophy in China
J Yuan, H Takashima, I Higuchi, et al.
Rinsho Hoshasen. Clinical Radiography
|
January 1, 1989
[CT-guided transcutaneous lung biopsy]
Y Kawase, K Satoh, H Seo, et al.
Acta Neuropathologica
|
January 1, 1986
Ultrastructural study of the effect of calcium ionophore, A23187, on rat muscle
T Yoshimura, M Tsujihata, A Satoh, et al.
Page
of 26
Search research articles
Search
Showing results (131-140 of 252) with videos related to
Sort By:
Page
of 26
Journal of Human Genetics
|
June 8, 2001
Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant connexin 32 (GJB1)
W Matsuyama, M Nakagawa, T Moritoyo, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
September 1, 1987
[Quantification of plasminogen activator antigen in plasma by ELISA and age-related changes in its concentration]
M Soma, Y Maeda, M Ueda, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
March 23, 1999
Loss of 123I-MIBG uptake by the heart in Parkinson's disease: assessment of cardiac sympathetic denervation and diagnostic value
A Satoh, T Serita, M Seto, et al.
Experimental Neurology
|
December 1, 1993
Immortalized GABAergic cell lines derived from rat striatum using a temperature-sensitive allele of the SV40 large T antigen
M Giordano, H Takashima, A Herranz, et al.
Journal of the Neurological Sciences
|
March 27, 2001
Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence
M Nakagawa, H Takashima, F Umehara, et al.
Acta Neurologica Scandinavica
|
July 1, 1992
Systemic interferon-alpha in the treatment of HTLV-I-associated myelopathy
Y Kuroda, K Kurohara, F Fujiyama, et al.
Clinical Nuclear Medicine
|
August 26, 1998
False-positive iodine-131 whole-body imaging due to gestational sac
Y Nishiyama, Y Yamamoto, K Takahashi, et al.
Neuropediatrics
|
March 19, 2009
Genetically confirmed patients with merosin-deficient congenital muscular dystrophy in China
J Yuan, H Takashima, I Higuchi, et al.
Rinsho Hoshasen. Clinical Radiography
|
January 1, 1989
[CT-guided transcutaneous lung biopsy]
Y Kawase, K Satoh, H Seo, et al.
Acta Neuropathologica
|
January 1, 1986
Ultrastructural study of the effect of calcium ionophore, A23187, on rat muscle
T Yoshimura, M Tsujihata, A Satoh, et al.
Page
of 26