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Keiji Kurokawa

Showing results (1-10 of 7) with videos related to

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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Prevalence of Mutations in the FGFR3 Gene in Individuals with Idiopathic Short StatureMitsukazu Mamada, Tohru Yorifuji, Keiji Kurokawa, et al.
Human Genetics|October 7, 2006
Fibrillin I gene polymorphism is associated with tall stature of normal individualsMitsukazu Mamada, Tohru Yorifuji, Junko Yorifuji, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2004
Neonatal diabetes mellitus and neonatal polycystic, dysplastic kidneys: Phenotypically discordant recurrence of a mutation in the hepatocyte nuclear factor-1beta gene due to germline mosaicismTohru Yorifuji, Keiji Kurokawa, Mitsukazu Mamada, et al.
The Journal of Clinical Endocrinology and Metabolism|March 24, 2005
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 mellitusTohru Yorifuji, Kazuaki Nagashima, Keiji Kurokawa, et al.
Human Genetics|August 22, 2002
Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implicationsTohru Yorifuji, Masahiko Kawai, Junko Muroi, et al.
European Journal of Pediatrics|May 17, 2006
Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiencyHironori Nagasaka, Tohru Yorifuji, Kei Murayama, et al.
Journal of Human Genetics|February 21, 2007
Molecular and clinical analyses of Japanese patients with carbamoylphosphate synthetase 1 (CPS1) deficiencyKeiji Kurokawa, Tohru Yorifuji, Masahiko Kawai, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
Prevalence of Mutations in the FGFR3 Gene in Individuals with Idiopathic Short StatureMitsukazu Mamada, Tohru Yorifuji, Keiji Kurokawa, et al.
Human Genetics|October 7, 2006
Fibrillin I gene polymorphism is associated with tall stature of normal individualsMitsukazu Mamada, Tohru Yorifuji, Junko Yorifuji, et al.
The Journal of Clinical Endocrinology and Metabolism|June 8, 2004
Neonatal diabetes mellitus and neonatal polycystic, dysplastic kidneys: Phenotypically discordant recurrence of a mutation in the hepatocyte nuclear factor-1beta gene due to germline mosaicismTohru Yorifuji, Keiji Kurokawa, Mitsukazu Mamada, et al.
The Journal of Clinical Endocrinology and Metabolism|March 24, 2005
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 mellitusTohru Yorifuji, Kazuaki Nagashima, Keiji Kurokawa, et al.
Human Genetics|August 22, 2002
Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implicationsTohru Yorifuji, Masahiko Kawai, Junko Muroi, et al.
European Journal of Pediatrics|May 17, 2006
Effects of arginine treatment on nutrition, growth and urea cycle function in seven Japanese boys with late-onset ornithine transcarbamylase deficiencyHironori Nagasaka, Tohru Yorifuji, Kei Murayama, et al.
Journal of Human Genetics|February 21, 2007
Molecular and clinical analyses of Japanese patients with carbamoylphosphate synthetase 1 (CPS1) deficiencyKeiji Kurokawa, Tohru Yorifuji, Masahiko Kawai, et al.
Pageof 1