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R Minami

Showing results (141-150 of 184) with videos related to

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Annals of Vascular Surgery|July 10, 2025
Projected Survival Benefit of Fenestrated Endovascular Aneurysm Repair versus Observation for Complex Abdominal Aortic Aneurysms in Patients with Limited Life ExpectancyHataka R Minami, Erin K Greenleaf, Besma J Nejim, et al.
Internal Medicine (Tokyo, Japan)|February 16, 2000
A female carrier of Duchenne muscular dystrophy complicated with cardiomyopathyH Ogata, H Nakagawa, K Hamabe, et al.
The Journal of Clinical Investigation|May 1, 1993
Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophyN Narita, H Nishio, Y Kitoh, et al.
Archives of Virology|January 1, 1983
The polypeptide of a human calicivirusH Terashima, S Chiba, Y Sakuma, et al.
No to Hattatsu = Brain and Development|May 1, 1987
[An atypical case of group A xeroderma pigmentosum]N Tate, K Sasaki, T Kusano, et al.
No to Hattatsu = Brain and Development|May 1, 1988
[Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)--clinical features and the findings of nerve pathology]N Tachi, S Hosoya, K Sasaki, et al.
No to Hattatsu = Brain and Development|November 1, 1988
[Rigid spine syndrome: report of three cases]K Kameda, S Wakai, M Okabe, et al.
Vascular Medicine (London, England)|January 19, 2018
Cost-effectiveness analysis of asymptomatic peripheral artery disease screening with the ABI testNathan K Itoga, Hataka R Minami, Meenadachi Chelvakumar, et al.
Pediatric Neurology|January 1, 1989
Glycogen storage disease with normal acid maltase: skeletal and cardiac musclesN Tachi, M Tachi, K Sasaki, et al.
Neurology|September 1, 1994
Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotypeY Takeshima, H Nishio, N Narita, et al.
Pageof 19

Showing results (141-150 of 184) with videos related to

Sort By:
Pageof 19
Annals of Vascular Surgery|July 10, 2025
Projected Survival Benefit of Fenestrated Endovascular Aneurysm Repair versus Observation for Complex Abdominal Aortic Aneurysms in Patients with Limited Life ExpectancyHataka R Minami, Erin K Greenleaf, Besma J Nejim, et al.
Internal Medicine (Tokyo, Japan)|February 16, 2000
A female carrier of Duchenne muscular dystrophy complicated with cardiomyopathyH Ogata, H Nakagawa, K Hamabe, et al.
The Journal of Clinical Investigation|May 1, 1993
Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophyN Narita, H Nishio, Y Kitoh, et al.
Archives of Virology|January 1, 1983
The polypeptide of a human calicivirusH Terashima, S Chiba, Y Sakuma, et al.
No to Hattatsu = Brain and Development|May 1, 1987
[An atypical case of group A xeroderma pigmentosum]N Tate, K Sasaki, T Kusano, et al.
No to Hattatsu = Brain and Development|May 1, 1988
[Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)--clinical features and the findings of nerve pathology]N Tachi, S Hosoya, K Sasaki, et al.
No to Hattatsu = Brain and Development|November 1, 1988
[Rigid spine syndrome: report of three cases]K Kameda, S Wakai, M Okabe, et al.
Vascular Medicine (London, England)|January 19, 2018
Cost-effectiveness analysis of asymptomatic peripheral artery disease screening with the ABI testNathan K Itoga, Hataka R Minami, Meenadachi Chelvakumar, et al.
Pediatric Neurology|January 1, 1989
Glycogen storage disease with normal acid maltase: skeletal and cardiac musclesN Tachi, M Tachi, K Sasaki, et al.
Neurology|September 1, 1994
Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotypeY Takeshima, H Nishio, N Narita, et al.
Pageof 19