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Mitsukazu Mamada

Showing results (11-20 of 19) with videos related to

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Cureus|August 1, 2024
Diphenhydramine Intoxication With Blood Extended Half-Life and a False Positive Result for Tricyclic AntidepressantsKoji Yokoyama, Asuka Kaizaki-Mitsumoto, Satoshi Numazawa, et al.
Cureus|October 20, 2025
Symptomatic Congenital Cytomegalovirus Infection in a Preterm Very-Low-Birth-Weight Infant Treated With Intravenous Ganciclovir Followed by Oral ValganciclovirHiroki Kita, Keisuke Maeda, Takayuki Nukada, et al.
Clinical Endocrinology|April 24, 2004
Earlier initiation of GH therapy does not influence adult height but enables earlier start of pubertal induction in children with multiple pituitary hormone deficiencyMasahiko Kawai, Toru Momoi, Mitsukazu Mamada, et al.
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.
American Journal of Medical Genetics|September 5, 2002
Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotypeAyumi Uematsu, Tohru Yorifuji, Junko Muroi, 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.
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.
The Journal of Clinical Endocrinology and Metabolism|September 26, 2024
Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 PatientsHiromune Narusawa, Tomoe Ogawa, Hideaki Yagasaki, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Cureus|August 1, 2024
Diphenhydramine Intoxication With Blood Extended Half-Life and a False Positive Result for Tricyclic AntidepressantsKoji Yokoyama, Asuka Kaizaki-Mitsumoto, Satoshi Numazawa, et al.
Cureus|October 20, 2025
Symptomatic Congenital Cytomegalovirus Infection in a Preterm Very-Low-Birth-Weight Infant Treated With Intravenous Ganciclovir Followed by Oral ValganciclovirHiroki Kita, Keisuke Maeda, Takayuki Nukada, et al.
Clinical Endocrinology|April 24, 2004
Earlier initiation of GH therapy does not influence adult height but enables earlier start of pubertal induction in children with multiple pituitary hormone deficiencyMasahiko Kawai, Toru Momoi, Mitsukazu Mamada, et al.
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.
American Journal of Medical Genetics|September 5, 2002
Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotypeAyumi Uematsu, Tohru Yorifuji, Junko Muroi, 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.
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.
The Journal of Clinical Endocrinology and Metabolism|September 26, 2024
Comprehensive Study on Central Precocious Puberty: Molecular and Clinical Analyses in 90 PatientsHiromune Narusawa, Tomoe Ogawa, Hideaki Yagasaki, et al.
Pageof 2