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Reiko Horikawa

Showing results (171-180 of 196) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|March 6, 2004
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patientsNaoko Sato, Noriyuki Katsumata, Masayo Kagami, et al.
Molecular Genetics and Metabolism|April 3, 2004
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118RKanako Kojima, Shigeo Kure, Fumiaki Kamada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 17, 2015
Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in JapanToshiaki Tanaka, Yutaka Igarashi, Keiichi Ozono, et al.
BMC Health Services Research|October 23, 2016
Effects of financial support on treatment of adolescents with growth hormone deficiency: a retrospective study in JapanEri Maeda, Takahiro Higashi, Tomonobu Hasegawa, et al.
Cytogenetic and Genome Research|June 4, 2019
DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number VariationsKenichiro Ogushi, Atsushi Hattori, Erina Suzuki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Favorable impact of growth hormone treatment on cholesterol levels in turner syndromeHitoshi Kohno, Yutaka Igarashi, Keiichi Ozono, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 2, 2017
Childbirth and fertility preservation in childhood and adolescent cancer patients: a second national survey of Japanese pediatric endocrinologistsYoko Miyoshi, Tohru Yorifuji, Reiko Horikawa, et al.
Nutrients|January 23, 2024
The Population-Attributable Fractions of Small-for-Gestational-Age Births: Results from the Japan Birth Cohort ConsortiumKazue Ishitsuka, Aurélie Piedvache, Sumitaka Kobayashi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 5, 2009
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patientsMaki Fukami, Gen Nishimura, Keiko Homma, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 24, 2016
Gonadal function, fertility, and reproductive medicine in childhood and adolescent cancer patients: a national survey of Japanese pediatric endocrinologistsYoko Miyoshi, Tohru Yorifuji, Reiko Horikawa, et al.
Pageof 20

Showing results (171-180 of 196) with videos related to

Sort By:
Pageof 20
The Journal of Clinical Endocrinology and Metabolism|March 6, 2004
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patientsNaoko Sato, Noriyuki Katsumata, Masayo Kagami, et al.
Molecular Genetics and Metabolism|April 3, 2004
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118RKanako Kojima, Shigeo Kure, Fumiaki Kamada, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 17, 2015
Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in JapanToshiaki Tanaka, Yutaka Igarashi, Keiichi Ozono, et al.
BMC Health Services Research|October 23, 2016
Effects of financial support on treatment of adolescents with growth hormone deficiency: a retrospective study in JapanEri Maeda, Takahiro Higashi, Tomonobu Hasegawa, et al.
Cytogenetic and Genome Research|June 4, 2019
DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number VariationsKenichiro Ogushi, Atsushi Hattori, Erina Suzuki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Favorable impact of growth hormone treatment on cholesterol levels in turner syndromeHitoshi Kohno, Yutaka Igarashi, Keiichi Ozono, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 2, 2017
Childbirth and fertility preservation in childhood and adolescent cancer patients: a second national survey of Japanese pediatric endocrinologistsYoko Miyoshi, Tohru Yorifuji, Reiko Horikawa, et al.
Nutrients|January 23, 2024
The Population-Attributable Fractions of Small-for-Gestational-Age Births: Results from the Japan Birth Cohort ConsortiumKazue Ishitsuka, Aurélie Piedvache, Sumitaka Kobayashi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 5, 2009
Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patientsMaki Fukami, Gen Nishimura, Keiko Homma, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 24, 2016
Gonadal function, fertility, and reproductive medicine in childhood and adolescent cancer patients: a national survey of Japanese pediatric endocrinologistsYoko Miyoshi, Tohru Yorifuji, Reiko Horikawa, et al.
Pageof 20