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Reiko Horikawa

Showing results (11-20 of 212) with videos related to

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Endocrine Journal|February 14, 2008
Novel missense mutation in the P-box of androgen receptor in a patient with androgen insensitivity syndromeNoriyuki Katsumata, Reiko Horikawa, Toshiaki Tanaka
Endocrine Journal|May 26, 2006
Replacement of alanine with asparagic acid at position 203 in human steroidogenic acute regulatory protein impairs the ability to enhance steroidogenesis in vitroNoriyuki Katsumata, Reiko Horikawa, Toshiaki Tanaka
Metabolism: Clinical and Experimental|April 29, 2010
Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiencyNoriyuki Katsumata, Takashi Shinagawa, Reiko Horikawa, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|November 26, 2018
Auxiliary Partial Orthotopic Liver Transplantation for Noncirrhotic Metabolic Liver Disease: Reigniting Interest in an Old but New TechniqueMureo Kasahara, Seisuke Sakamoto, Reiko Horikawa, et al.
Endocrine Journal|May 8, 2003
The comparison of the effects of short-term growth hormone treatment in patients with achondroplasia and with hypochondroplasiaNoriko Tanaka, Noriyuki Katsumata, Reiko Horikawa, et al.
Expert Opinion on Drug Delivery|October 11, 2016
Growth hormone delivery devices: current features and potential for enhanced treatment adherenceTilman R Rohrer, Reiko Horikawa, Anne-Marie Kappelgaard
Pediatrics International : Official Journal of the Japan Pediatric Society|April 13, 2017
Portosystemic shunt as a cause of congenital hyperinsulinemic hypoglycemiaKeisuke Yoshii, Masahiro Noda, Yasuhiro Naiki, et al.
American Journal of Medical Genetics. Part A|December 6, 2017
Biallelic mutations in LARS2 can cause Perrault syndrome type 2 with neurologic symptomsRika Kosaki, Reiko Horikawa, Eriko Fujii, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 18, 2022
Novel non-stop variant of the <i>NR0B1</i> gene in two siblings with adrenal hypoplasia congenitaTomoko Ota, Noriyuki Katsumata, Yasuhiro Naiki, et al.
Endocrine Journal|November 10, 2017
Mismatch between fetal sexing and birth phenotype: a case of complete androgen insensitivity syndromeKeisuke Yoshii, Yasuhiro Naiki, Yumiko Terada, et al.
Pageof 22

Showing results (11-20 of 212) with videos related to

Sort By:
Pageof 22
Endocrine Journal|February 14, 2008
Novel missense mutation in the P-box of androgen receptor in a patient with androgen insensitivity syndromeNoriyuki Katsumata, Reiko Horikawa, Toshiaki Tanaka
Endocrine Journal|May 26, 2006
Replacement of alanine with asparagic acid at position 203 in human steroidogenic acute regulatory protein impairs the ability to enhance steroidogenesis in vitroNoriyuki Katsumata, Reiko Horikawa, Toshiaki Tanaka
Metabolism: Clinical and Experimental|April 29, 2010
Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiencyNoriyuki Katsumata, Takashi Shinagawa, Reiko Horikawa, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|November 26, 2018
Auxiliary Partial Orthotopic Liver Transplantation for Noncirrhotic Metabolic Liver Disease: Reigniting Interest in an Old but New TechniqueMureo Kasahara, Seisuke Sakamoto, Reiko Horikawa, et al.
Endocrine Journal|May 8, 2003
The comparison of the effects of short-term growth hormone treatment in patients with achondroplasia and with hypochondroplasiaNoriko Tanaka, Noriyuki Katsumata, Reiko Horikawa, et al.
Expert Opinion on Drug Delivery|October 11, 2016
Growth hormone delivery devices: current features and potential for enhanced treatment adherenceTilman R Rohrer, Reiko Horikawa, Anne-Marie Kappelgaard
Pediatrics International : Official Journal of the Japan Pediatric Society|April 13, 2017
Portosystemic shunt as a cause of congenital hyperinsulinemic hypoglycemiaKeisuke Yoshii, Masahiro Noda, Yasuhiro Naiki, et al.
American Journal of Medical Genetics. Part A|December 6, 2017
Biallelic mutations in LARS2 can cause Perrault syndrome type 2 with neurologic symptomsRika Kosaki, Reiko Horikawa, Eriko Fujii, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 18, 2022
Novel non-stop variant of the <i>NR0B1</i> gene in two siblings with adrenal hypoplasia congenitaTomoko Ota, Noriyuki Katsumata, Yasuhiro Naiki, et al.
Endocrine Journal|November 10, 2017
Mismatch between fetal sexing and birth phenotype: a case of complete androgen insensitivity syndromeKeisuke Yoshii, Yasuhiro Naiki, Yumiko Terada, et al.
Pageof 22