Author

Kenichi Satomura

Observed names: K Satomura, K. Satomura, KENICHI SATOMURA, Ken-ichi Satomura, Kenichi SATOMURA

Observed institutions: Chiba University, Okayama University, Wakayama Medical University, Kyoto University, Osaka Prefectural Board of Education, Osaka Women's and Children's Hospital, Ome Municipal General Hospital, Kanagawa Children's Medical Center, National Center For Child Health and Development, Osaka University Hospital, Minoh City Hospital, Hara Genitourinary Hospital, Kobe University, The University of Osaka

OpenAlex ID: A5045306508

Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome

2005 · Mayumi Sako, Koichi Nakanishi, et al. · Kidney International · 93

Identification of novel missense mutations (Phe310Leu and Gly439Arg) in a neonatal case of hypophosphatasia

1996 · K Ozono, M Yamagata, et al. · The Journal of Clinical Endocrinology & Metabolism · 79

PAX2 Gene Mutation in a Family with Isolated Renal Hypoplasia

2001 · KAORI NISHIMOTO, KAZUMOTO IIJIMA, et al. · Journal of the American Society of Nephrology · 75

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

2003 · Kyoko Maruyama, Kazumoto Iijima, et al. · Pediatric Nephrology · 70

End-stage renal disease in Japanese children: a nationwide survey during 2006–2011

2015 · Motoshi Hattori, Mayumi Sako, et al. · Clinical and Experimental Nephrology · 69

The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies

2010 · Kandai Nozu, Kazumoto Iijima, et al. · The Journal of Clinical Endocrinology & Metabolism · 64

The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune?Albright syndrome

2005 · Takehisa Yamamoto, Yasuo Imanishi, et al. · Journal of Bone and Mineral Metabolism · 63

Analysis of Localization of Mutated Tissue-Nonspecific Alkaline Phosphatase Proteins Associated with Neonatal Hypophosphatasia Using Green Fluorescent Protein Chimeras

1998 · Guiming Cai, Toshimi Michigami, et al. · The Journal of Clinical Endocrinology & Metabolism · 57

Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Large Heterozygous Deletions With Semiquantitative PCR

2007 · Kandai Nozu, Xue Jun Fu, et al. · Pediatric Research · 48

Novel mutations in the a3 subunit of vacuolar H+-adenosine triphosphatase in a Japanese patient with infantile malignant osteopetrosis

2002 · T Michigami, T Kageyama, et al. · Bone · 47

Effect of Dibutyryl Adenosine 3′,5′-Monophosphate Administration on Plasma Concentrations of 1,25-Dihydroxyvitamin D in Pseudohypoparathyroidism Type I*

1981 · KANJI YAMAOKA, YOSHIKI SEINO, et al. · The Journal of Clinical Endocrinology & Metabolism · 45

Structural Basis and Genotype–Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance

2017 · Jun Hosoe, Hiroko Kadowaki, et al. · Diabetes · 44

Risk factors for developing severe clinical course in HUS patients: a national survey in Japan

2008 · Ichiro Kamioka, Kunihiko Yoshiya, et al. · Pediatrics International · 39

Abnormal relationship between serum phosphate concentration and renal 25-hydroxycholecalciferol-1-alpha-hydroxylase activity in X-linked hypophosphatemic mice.

1986 · K Yamaoka, Y Seino, et al. · PubMed · 39

Increased Serum IL-10 and Endothelin Levels in Hemolytic Uremic Syndrome Caused by Escherichia coli O157

2000 · Takehisa Yamamoto, Ken-ichi Nagayama, et al. · The Nephron journals/Nephron journals · 33

A further case of renal tubular dysgenesis surviving the neonatal period

2008 · Mitsugu Uematsu, Osamu Sakamoto, et al. · European Journal of Pediatrics · 31

Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan

2016 · Yukiko Hashimoto, Sumito Dateki, et al. · Pediatric Diabetes · 30

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Effect of 1,25-Dihydroxyvitamin D3on Insulin Secretion: Direct or Mediated?

1986 · YOSHIYUKI TANAKA, YOSHIKI SEINO, et al. · Endocrinology · 30

EYA1 and SIX1 gene mutations in Japanese patients with branchio-oto-renal (BOR) syndrome and related conditions

2006 · Michiyo Okada, Rika Fujimaru, et al. · Pediatric Nephrology · 28

Renal 25-hydroxyvitamin D3-1-hydroxylase in patients with renal disease

1988 · Kenichi Satomura, Yoshiki Seino, et al. · Kidney International · 26

Hypercalcemia associated with infantile fibrosarcoma producing parathyroid hormone-related protein

1996 · T Michigami, H Yamato, et al. · The Journal of Clinical Endocrinology & Metabolism · 22

Sequence-Based Diagnosis of Tyrosinase-Related Oculocutaneous Albinism: Successful Sequence Analysis of the Tyrosinase Gene from Blood Spots Dried on Filter Paper

1998 · J. Matsunaga, M. Dakeishi-Hara, et al. · Dermatology · 19

The circadian rhythms of blood ionized calcium in humans

1983 · M. Ishida, Y. Seino, et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 18

Risk factors for neurological complications in complete hemolytic uremic syndrome caused by Escherichia coli O157

2008 · Takehisa Yamamoto, Kenichi Satomura, et al. · Pediatrics International · 16

Proteinuria and glomerular hypertrophy in extremely low‐birthweight children

2014 · Asako Hayashi, Yoko Santo, et al. · Pediatrics International · 14

Works count: 65

Citation count: 1,200

H-index: 21

I10-index: 28