Kiyoshi Omura - Concepedia

Author

Kiyoshi Omura

National Center of Neurology and Psychiatry

Also Known As

K Omura, K. OMURA, K. Omura, KIYOSHI OMURA, Kiyoshi OMURA, Kiyoshi Omura

Publications

631

Citations

H-Index

Concepts

All Affiliations

National Center of Neurology and Psychiatry Tohoku University Sendai Nishitaga National Hospital Osaka City University Takeda (Japan)

About

Kiyoshi Omura is an author at National Center of Neurology and Psychiatry specializing in medicine, biochemistry, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	363
2	Natural Sciences	6	6	117
3	Engineering	3	3	114
4	Health Sciences	2	2	22
5	Public Health	2	2	47

Kiyoshi Omura

Publications

547

Citations

H-Index

Page 1

	Year	Citations
Separation of Selenium-Containing Proteins in Human and Mouse Plasma Using Tandem High-Performance Liquid Chromatography Columns Coupled with Inductively Coupled Plasma-Mass Spectrometry Hiroshi Koyama, Kiyoshi Omura, Akiko Ejima, Analytical Biochemistry EngineeringBiochemistrySelenium DeficiencyMedicineBioanalysis	1999	89
The comparison between pains, difficulties in function, and associating factors of patients in subtypes of temporomandibular disorders Koji Kino, Masayasu Sugisaki, Tadasu Haketa, Journal of Oral Rehabilitation	2005	87
Characteristics of the increase in plasma brain natriuretic peptide level in left ventricular systolic dysfunction, associated with muscular dystrophy in comparison with idiopathic dilated cardiomyopathy Jun Demachi, Yutaka Kagaya, Jun Watanabe, Neuromuscular Disorders CardiomyopathyHeart FailureCardiovascular DiseasePhysiologyCardiovascular Function	2004	36
Efficacy of idebenone for respiratory failure in a patient with Leigh syndrome: A long-term follow-up study Kazuhiro Haginoya, Shigeaki Miyabayashi, Masahiro Kikuchi, Journal of the Neurological Sciences MedicineRespiratory FailureLong-term Follow-up StudyLeigh Syndrome	2008	32
GMl-gangliosidosis: Abnormalities in biosynthesis and early processing of β-galactosidase in fibroblasts Eiji Nanba, Akihiko Tsuji, Kiyoshi Omura, Biochemical and Biophysical Research Communications BiosynthesisBiochemistryEarly ProcessingNatural SciencesGlycobiology	1988	27
Lysine Malabsorption Syndrome: A New Type of Transport Defect Kiyoshi Omura, Nobuko Yamanaka, Shinobu Higami, PEDIATRICS UrologyTransport DefectAmino AcidsRenal FunctionVoiding Dysfunction	1976	26
Hyperalaninemia with Pyruvicemia in a Patient Suggestive of Leigh's Encephalomyelopathy Keiya Tada, KATSUHIRO SUGITA, Ken Fujitani, The Tohoku Journal of Experimental Medicine MedicinePhysiologyInherited Metabolic DiseasePyruvate LevelPathology	1973	26
Galactosialidosis: A direct evidence that a 46-kilodalton protein restores deficient enzyme activities in fibroblasts Eiji Nanba, Akihiko Tsuji, Kiyoshi Omura, Biochemical and Biophysical Research Communications 46-Kilodalton ProteinBiosynthesisCellular EnzymologyBiochemistryMedicine	1987	25
Intracellular Transport of Acid α-Glucosidase in Human Fibroblasts: Evidencefor Involvement of Phosphomannosyl Receptor-Independent System1 Akihiko Tsuji, Kiyoshi Omura, Yoshiyuki Suzuki The Journal of Biochemistry Protein SecretionGlycobiologyCellular PhysiologyMembrane TransportAutophagy	1988	22
Km mutant of acid α‐glucosidase in a case of cardiomyopathy without signs of skeletal muscle involvement Yoshiyuki Suzuki, Akihiko Tsuji, Kiyoshi Omura, Clinical Genetics	1988	22

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