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Ikuma Fujiwara

Showing results (21-30 of 74) with videos related to

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Congenital Anomalies|November 12, 2014
Association of achondroplasia with Down syndrome: difficulty in prenatal diagnosis by sonographic and 3-D helical computed tomographic analysesAkimune Kaga, Jun Murotsuki, Miki Kamimura, et al.
The Tohoku Journal of Experimental Medicine|November 2, 2006
Reduced exposure to mercury in patients receiving enteral nutritionMitsutoshi Munakata, Akira Onuma, Kazuhiro Haginoya, et al.
European Journal of Endocrinology|October 25, 2014
Heterozygous defects in PAX6 gene and congenital hypopituitarismMasaki Takagi, Keisuke Nagasaki, Ikuma Fujiwara, et al.
Cytogenetic and Genome Research|March 3, 2017
Xp22.31 Microdeletion due to Microhomology-Mediated Break-Induced Replication in a Boy with Contiguous Gene Deletion SyndromeKoki Nagai, Hirohito Shima, Miki Kamimura, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 2006
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosteroneKeiko Homma, Tomonobu Hasegawa, Toshiro Nagai, et al.
Reproductive Toxicology (Elmsford, N.Y.)|January 25, 2020
The association between gestational use of personal care products and neonatal urological abnormality at birth: The Japan Environment and Children's StudyYukiko Nishihama, Nozomi Tatsuta, Miyuki Iwai-Shimada, et al.
American Journal of Medical Genetics. Part A|July 2, 2015
A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondylyMasaki Takagi, Masanori Kouwaki, Koya Kawase, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 11, 2019
A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1Akiko Saito-Hakoda, Junko Kanno, Dai Suzuki, et al.
Journal of the Neurological Sciences|December 15, 2011
Hypoperfusion in caudate nuclei in patients with brain-lung-thyroid syndromeMitsugu Uematsu, Kazuhiro Haginoya, Atsuo Kikuchi, et al.
Endocrine Journal|April 29, 2024
A case of 49,XXXYY followed-up from infancy to adulthood with review of literatureJunko Kanno, Akinobu Miura, Sayaka Kawashima, et al.
Pageof 8

Showing results (21-30 of 74) with videos related to

Sort By:
Pageof 8
Congenital Anomalies|November 12, 2014
Association of achondroplasia with Down syndrome: difficulty in prenatal diagnosis by sonographic and 3-D helical computed tomographic analysesAkimune Kaga, Jun Murotsuki, Miki Kamimura, et al.
The Tohoku Journal of Experimental Medicine|November 2, 2006
Reduced exposure to mercury in patients receiving enteral nutritionMitsutoshi Munakata, Akira Onuma, Kazuhiro Haginoya, et al.
European Journal of Endocrinology|October 25, 2014
Heterozygous defects in PAX6 gene and congenital hypopituitarismMasaki Takagi, Keisuke Nagasaki, Ikuma Fujiwara, et al.
Cytogenetic and Genome Research|March 3, 2017
Xp22.31 Microdeletion due to Microhomology-Mediated Break-Induced Replication in a Boy with Contiguous Gene Deletion SyndromeKoki Nagai, Hirohito Shima, Miki Kamimura, et al.
The Journal of Clinical Endocrinology and Metabolism|April 13, 2006
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosteroneKeiko Homma, Tomonobu Hasegawa, Toshiro Nagai, et al.
Reproductive Toxicology (Elmsford, N.Y.)|January 25, 2020
The association between gestational use of personal care products and neonatal urological abnormality at birth: The Japan Environment and Children's StudyYukiko Nishihama, Nozomi Tatsuta, Miyuki Iwai-Shimada, et al.
American Journal of Medical Genetics. Part A|July 2, 2015
A novel mutation Ser344Cys in FGFR3 causes achondroplasia with severe platyspondylyMasaki Takagi, Masanori Kouwaki, Koya Kawase, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 11, 2019
A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1Akiko Saito-Hakoda, Junko Kanno, Dai Suzuki, et al.
Journal of the Neurological Sciences|December 15, 2011
Hypoperfusion in caudate nuclei in patients with brain-lung-thyroid syndromeMitsugu Uematsu, Kazuhiro Haginoya, Atsuo Kikuchi, et al.
Endocrine Journal|April 29, 2024
A case of 49,XXXYY followed-up from infancy to adulthood with review of literatureJunko Kanno, Akinobu Miura, Sayaka Kawashima, et al.
Pageof 8