Harumasa Nakamura - Concepedia

Author

Harumasa Nakamura

National Center of Neurology and Psychiatry ORCID

Also Known As

H Nakamura, H. NAKAMURA, H. Nakamura, H.N. Nakamura, Harumasa NAKAMURA, Harumasa Nakamura, Hirofumi Komaki, Nakamura, Harumasa

178

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

National Center of Neurology and Psychiatry Tokyo Women's Medical University The University of Osaka The University of Tokyo Kyoto University

About

Harumasa Nakamura is an author at National Center of Neurology and Psychiatry specializing in medicine, pharmacology, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	366
2	Engineering	3	3	124
3	Health Sciences	2	2	71
4	Natural Sciences	1	1	117
5	Public Health	1	1	16

Harumasa Nakamura

Publications

Citations

H-Index

Page 1

	Year	Citations
Systemic administration of the antisense oligonucleotide NS-065/NCNP-01 for skipping of exon 53 in patients with Duchenne muscular dystrophy Hirofumi Komaki, Tetsuya Nagata, Takashi Saito, Science Translational Medicine	2018	150
Subcellular characteristics of phospholipase A2 activity in the rat kidney. Enhanced cytosolic, mitochondrial, and microsomal phospholipase A2 enzymatic activity after renal ischemia and reperfusion. Harumasa Nakamura, Raphael A. Nemenoff, J H Gronich, Journal of Clinical Investigation Renal IschemiaLipid PeroxidationRenal PathologyPhospholipase A2Oxidative Stress	1991	117
Effect of welding speed on microstructural and mechanical properties of laser lap weld joints in dissimilar Al and Cu sheets Su-Jin Lee, Harumasa Nakamura, Yousuke Kawahito, Science and Technology of Welding & Joining Materials ScienceAdvanced Laser ProcessingFriction WeldingEngineeringDissimilar Al	2013	103
Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy) Harumasa Nakamura, En Kimura, Madoka Mori‐Yoshimura, Orphanet Journal of Rare Diseases	2013	73
Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan Mariko Okubo, Kanako Goto, Hirofumi Komaki, Orphanet Journal of Rare Diseases	2017	59
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, Journal of the Neurological Sciences GeneticsMendelian DisorderMolecular BiologyGne Gene Result	2012	54
Nationwide patient registry for GNE myopathy in Japan Madoka Mori‐Yoshimura, Yukiko Hayashi, Naohiro Yonemoto, Orphanet Journal of Rare Diseases	2014	52
Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy Mariko Okubo, S. Noguchi, Shinichiro Hayashi, Human Genetics	2020	45
Long-term effect of repeated lidocaine injections into the external oblique for upper camptocormia in Parkinson's disease Yoshihiko Furusawa, Yohei Mukai, Tomoya Kawazoe, Parkinsonism & Related Disorders Lidocaine InjectionsLong-term EffectMedicineExternal ObliqueNeuropharmacology	2012	43
Heparin-enhanced plasma phospholipase A2 activity and prostacyclin synthesis in patients undergoing cardiac surgery. Harumasa Nakamura, Dong Kun Kim, Daniel M. Philbin, Journal of Clinical Investigation Heart FailureCardiovascular PharmacologyCpb PeriodSurgeryPharmacotherapy	1995	42

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