Takeshi Matsuyama - Concepedia

Author

Takeshi Matsuyama

Also Known As

Hiroshi Hataya, Hitoshi Nakazato, Koichi Nakanishi, Matsuyama Takeshi, Motohiro Arai, TAKESHI MATSUYAMA, Takeshi MATSUYAMA, Takeshi Matsuyama, Tomoko Horinouchi, Tsutomu Ichinose

Publications

2.5K

Citations

H-Index

118

Concepts

All Affiliations

Nara Medical University National Center For Child Health and Development Tokyo Metropolitan Children's Medical Center The University of Tokyo Kobe University

About

Takeshi Matsuyama is an author at Nara Medical University specializing in medicine, neurology, and nephrology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	26	1.2K
2	Health Sciences	4	4	178
3	Public Health	4	4	244
4	Engineering	2	2	30
5	Social Sciences	1	1	86

Takeshi Matsuyama

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Urinary Megalin Deficiency Implicates Abnormal Tubular Endocytic Function in Fanconi Syndrome Anthony G.W. Norden, Marta Lapsley, Takashi Igarashi, Journal of the American Society of Nephrology	2002	127
Catechin Safely Improved Higher Levels of Fatness, Blood Pressure, and Cholesterol in Children Takeshi Matsuyama, Yuriko Tanaka, Isamu Kamimaki, Obesity	2008	114
Age, gender, and body length effects on reference serum creatinine levels determined by an enzymatic method in Japanese children: a multicenter study Osamu Uemura, Masataka Honda, Takeshi Matsuyama, Clinical and Experimental Nephrology ObesityNutritionBody Length EffectsJapanese ChildrenBody Composition	2011	111
Comparison of C1–2 posterior fusion and decompression of the vertebral artery in the treatment of bow hunter's stroke Takeshi Matsuyama, Tetsuya Morimoto, Toshisuke Sakaki Journal of neurosurgery	1997	110
Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease Takashi Sekine, Mutsuko Konno, Satoshi Sasaki, Kidney International Glomerular DiseaseGlomerulonephritisUrologyEpstein–fechtner SyndromesMyh9 R702 Mutations	2010	105
Clinical Practice Guidebook for Diagnosis and Treatment of Chronic Kidney Disease Seiichi Matsuo, Tsuyoshi Watanabe, Yasuhiko Iino, Clinical and Experimental Nephrology Glomerular DiseaseGlomerulonephritisHemodialysisRenal FunctionRenal Disease	2009	90
Chronic Schwann Cell Denervation and the Presence of a Sensory Nerve Reduce Motor Axonal Regeneration Olawale A.R. Sulaiman, Rajiv Midha, Catherine A. Munro, Experimental Neurology NeuroregenerationPeripheral Nerve InjuryNeuroanatomyRehabilitationNeurology	2002	86
Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis Naoko Akuta, Sarah E. Lloyd, Takashi Igarashi, Kidney International Japanese ChildrenGenetic DisorderMedicineGeneticsRenal Pathology	1997	82
The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia Fusako Komoda, Takashi Sekine, Jun Inatomi, Pediatric Nephrology UrologyRenal FunctionW258x MutationMedicineGenetics	2004	82
Transorbital Penetrating Injury by a Chopstick. Case Report. Takeshi Matsuyama, Kazuo Okuchi, Keiji Nogami, Neurologia medico-chirurgica SurgeryInjury PreventionAnatomyCraniomaxillofacial TraumaFacial Trauma	2001	73

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