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Ikuma Fujiwara

Showing results (11-20 of 74) with videos related to

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Pediatric Blood & Cancer|February 24, 2006
PTHrP-independent hypercalcemia with increased proinflammatory cytokines and bone resorption in two children with CD19-negative precursor B acute lymphoblastic leukemiaHidetaka Niizuma, Kunihiro Fujii, Atsushi Sato, et al.
Nephrology (Carlton, Vic.)|April 23, 2013
Phenotype variability in nephrogenic diabetes insipidus due to p.D85N mutation in the arginine vasopressin receptor 2 geneTetsuji Morimoto, Makiko Nakayama, Ikuma Fujiwara, et al.
Endocrine Journal|September 9, 2006
Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutationTsutomu Ogata, Ikuma Fujiwara, Eishin Ogawa, et al.
Endocrine Journal|August 23, 2008
Hypospadias in a male patient with 21-hydroxylase deficiencyKanako Kojima-Ishii, Ikuma Fujiwara, Noriyuki Katsumata, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 7, 2018
A follow-up during puberty in a Japanese girl with type A insulin resistance due to a novel mutation in <i>INSR</i>Akiko Saito-Hakoda, Aki Nishii, Takashi Uchida, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 31, 2013
Brain white matter abnormality in a newborn infant with congenital adrenal hyperplasiaAkimune Kaga, Akiko Saito-Hakoda, Mitsugu Uematsu, et al.
European Journal of Pediatrics|January 26, 2002
Normal pituitary function in a Japanese patient with Barth syndromeYuriko Katsushima, Ikuma Fujiwara, Osamu Sakamoto, et al.
Endocrine Journal|March 10, 2024
Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in JapanNao Shibata, Chikahiko Numakura, Takashi Hamajima, et al.
Hormone Research in Paediatrics|June 10, 2025
Functional non-coding variants in a TTTG microsatellite on chromosome 15q26.1 are a common genetic etiology of congenital hypothyroidism with thyroid gland in situHirohito Shima, Tomohiro Nakagawa, Kanako Kojima-Ishii, et al.
Brain & Development|April 18, 2006
A preliminary analysis of trace elements in the scalp hair of patients with severe motor disabilities receiving enteral nutritionMitsutoshi Munakata, Akira Onuma, Yasuko Kobayashi, et al.
Pageof 8

Showing results (11-20 of 74) with videos related to

Sort By:
Pageof 8
Pediatric Blood & Cancer|February 24, 2006
PTHrP-independent hypercalcemia with increased proinflammatory cytokines and bone resorption in two children with CD19-negative precursor B acute lymphoblastic leukemiaHidetaka Niizuma, Kunihiro Fujii, Atsushi Sato, et al.
Nephrology (Carlton, Vic.)|April 23, 2013
Phenotype variability in nephrogenic diabetes insipidus due to p.D85N mutation in the arginine vasopressin receptor 2 geneTetsuji Morimoto, Makiko Nakayama, Ikuma Fujiwara, et al.
Endocrine Journal|September 9, 2006
Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutationTsutomu Ogata, Ikuma Fujiwara, Eishin Ogawa, et al.
Endocrine Journal|August 23, 2008
Hypospadias in a male patient with 21-hydroxylase deficiencyKanako Kojima-Ishii, Ikuma Fujiwara, Noriyuki Katsumata, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 7, 2018
A follow-up during puberty in a Japanese girl with type A insulin resistance due to a novel mutation in <i>INSR</i>Akiko Saito-Hakoda, Aki Nishii, Takashi Uchida, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 31, 2013
Brain white matter abnormality in a newborn infant with congenital adrenal hyperplasiaAkimune Kaga, Akiko Saito-Hakoda, Mitsugu Uematsu, et al.
European Journal of Pediatrics|January 26, 2002
Normal pituitary function in a Japanese patient with Barth syndromeYuriko Katsushima, Ikuma Fujiwara, Osamu Sakamoto, et al.
Endocrine Journal|March 10, 2024
Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in JapanNao Shibata, Chikahiko Numakura, Takashi Hamajima, et al.
Hormone Research in Paediatrics|June 10, 2025
Functional non-coding variants in a TTTG microsatellite on chromosome 15q26.1 are a common genetic etiology of congenital hypothyroidism with thyroid gland in situHirohito Shima, Tomohiro Nakagawa, Kanako Kojima-Ishii, et al.
Brain & Development|April 18, 2006
A preliminary analysis of trace elements in the scalp hair of patients with severe motor disabilities receiving enteral nutritionMitsutoshi Munakata, Akira Onuma, Yasuko Kobayashi, et al.
Pageof 8