Kenichi Satomura - Concepedia

Author

Kenichi Satomura

Osaka International Cancer Institute

Also Known As

K Satomura, K. Satomura, KENICHI SATOMURA, Ken-ichi Satomura, Kenichi SATOMURA, Kenichi Satomura

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Osaka International Cancer Institute The University of Osaka Wakayama Medical University Kobe University National Center For Child Health and Development

About

Kenichi Satomura is an author at Osaka International Cancer Institute specializing in medicine, pathology, and nephrology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	657
2	Health Sciences	4	4	167
3	Biochemistry	1	1	39
4	Biology	1	1	71
5	Cell Biology	1	1	47

Kenichi Satomura

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome Mayumi Sako, Koichi Nakanishi, Mina Obana, Kidney International GlomerulonephritisUrologyGenetic DisorderCongenital Nephrotic SyndromeGenetics	2005	91
PAX2 Gene Mutation in a Family with Isolated Renal Hypoplasia Kaori Nishimoto, Kazumoto Iijima, Taku Shirakawa, Journal of the American Society of Nephrology	2001	75
Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia. Keiichi Ozono, Masayo Yamagata, Toshimi Michigami, The Journal of Clinical Endocrinology & Metabolism BiologySerum Alkaline PhosphataseMendelian DisorderGenetic DisorderGenetics	1996	71
NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children Kyoko Maruyama, Kazumoto Iijima, Masahiro Ikeda, Pediatric Nephrology Genetic DisorderMedicineGeneticsRenal PathologyGenetic Epidemiology	2003	70
The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome Takehisa Yamamoto, Yasuo Imanishi, Eiichi Kinoshita, Journal of Bone and Mineral Metabolism Metabolic SyndromeMetabolic DisorderVitamin D MetabolismPhysiologyParathyroid Hormone	2005	66
The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies Kandai Nozu, Kazumoto Iijima, Kyoko Kanda, The Journal of Clinical Endocrinology & Metabolism	2010	62
End-stage renal disease in Japanese children: a nationwide survey during 2006–2011 Motoshi Hattori, Mayumi Sako, Tetsuji Kaneko, Clinical and Experimental Nephrology GlomerulonephritisHemodialysisUrologyRenal DiseaseJapanese Children	2015	59
Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Large Heterozygous Deletions With Semiquantitative PCR Kandai Nozu, Xue Jun Fu, Koichi Nakanishi, Pediatric Research Mendelian DisorderGenetic DisorderGeneticsPathogenesisMolecular Analysis	2007	49
Analysis of Localization of Mutated Tissue-Nonspecific Alkaline Phosphatase Proteins Associated with Neonatal Hypophosphatasia Using Green Fluorescent Protein Chimeras1 Guiming Cai, Toshimi Michigami, Takehisa Yamamoto, The Journal of Clinical Endocrinology & Metabolism	1998	49
Novel mutations in the a3 subunit of vacuolar H+-adenosine triphosphatase in a Japanese patient with infantile malignant osteopetrosis Toshimi Michigami, Takashi Kageyama, Kenichi Satomura, Bone A3 SubunitNovel MutationsMolecular BiologyPathologyMedicine	2002	47

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