Keiji Kurokawa

Kyoto University — Japan

Biochemistry, Genetics and Molecular Biology · Life Sciences

9h-index507citations14works0.02yr avg
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Research Topics

Metabolism and Genetic Disorders(4), Diabetes Management and Research(2), Pancreatic function and diabetes(2), Connective tissue disorders research(2), RNA modifications and cancer(2)

Publications14 total

High-Density β-FeSi<sub>2</sub> crystals with 3D alignment fabricated by an oscillating magnetic field
IOP Conference Series Materials Science and Engineering·2018Open Access
Evaluation of new commercial immunochromatography kit for norovirus in feces
Pediatrics International·2009· 29 cited
Development study of a novel tower-style tank for simultaneous storing warm water and ice
Lecture notes in physics·2007
Molecular and clinical analyses of Japanese patients with carbamoylphosphate synthetase 1 (CPS1) deficiency
Journal of Human Genetics·2007· 42 citedOpen Access
Fibrillin I gene polymorphism is associated with tall stature of normal individuals
Human Genetics·2006· 13 cited
Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiency
European Journal of Pediatrics·2006· 42 cited
Prevalence of Mutations in the FGFR3 Gene in Individuals with Idiopathic Short Stature
Clinical Pediatric Endocrinology·2006· 9 citedOpen Access
The C42R Mutation in the Kir6.2 (KCNJ11) Gene as a Cause of Transient Neonatal Diabetes, Childhood Diabetes, or Later-Onset, Apparently Type 2 Diabetes Mellitus
The Journal of Clinical Endocrinology & Metabolism·2005· 122 citedOpen Access
Neonatal Diabetes Mellitus and Neonatal Polycystic, Dysplastic Kidneys: Phenotypically Discordant Recurrence of a Mutation in the Hepatocyte Nuclear Factor-1β Gene Due to Germline Mosaicism
The Journal of Clinical Endocrinology & Metabolism·2004· 130 citedOpen Access
A Method for Automatic Extracting Intracranial Region in MR Brain Image
IEEJ Transactions on Electronics Information and Systems·2004· 2 citedOpen Access
[Not Available].
PubMed·2003
Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications
Human Genetics·2003· 1 cited
Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications
Human Genetics·2002· 55 cited
Elevated serum interferon γ and interleukin‐6 in patients with necrotizing lymphadenitis (Kikuchi's disease)
British Journal of Haematology·1996· 62 cited

Frequent Co-authors

Tohru Yorifuji(9), Tatsutoshi Nakahata(8), Masahiko Kawai(7), Mitsukazu Mamada(5), Toru Momoi(3), Tsuyoshi Imai(2), Junko Muroi(2), Yosuke Shigematsu(2), Satoko Hirano(2), Nobuo Sakura(2), Ichiro Yoshida(2), Tomiko Kuhara(2), Fumio Endo(2), Hiroshi Mitsubuchi(2), Hironori Nagasaka(2), Shigenori Yamamoto(2), Masanori Adachi(2), Masaki Takayanagi(2), Yoshikazu Nishi(1), Seiichiro Shishido(1)