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Reiko Horikawa

Showing results (151-160 of 212) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patientsMasayo Kagami, Keisuke Nagasaki, Rika Kosaki, et al.
Pediatric Transplantation|October 18, 2014
Two-step transplantation for primary hyperoxaluria: a winning strategy to prevent progression of systemic oxalosis in early onset renal insufficiency casesKengo Sasaki, Seisuke Sakamoto, Hajime Uchida, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2004
Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndromeRie Yoshida, Tomonobu Hasegawa, Yukihiro Hasegawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Adult heights of 258 girls with turner syndrome on low dose of growth hormone therapy in JapanKeinosuke Fujita, Susumu Yokoya, Kenji Fujieda, et al.
Pediatric Transplantation|November 7, 2024
The Impact of Early Indication of Living Donor Liver Transplantation on the Outcomes of Patients With Propionic Acidemia: A Single-Center ExperienceToshimasa Nakao, Seisuke Sakamoto, Seiichi Shimizu, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision), , , et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 22, 2020
A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivorsYoko Miyoshi, Tohru Yorifuji, Chikako Shimizu, et al.
The Journal of Clinical Endocrinology and Metabolism|June 3, 2016
Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1bAkie Nakamura, Erika Hamaguchi, 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, 2013
Hepatocyte transplantation using a living donor reduced graft in a baby with ornithine transcarbamylase deficiency: a novel source of hepatocytesShin Enosawa, Reiko Horikawa, Akiko Yamamoto, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision), , , et al.
Pageof 22

Showing results (151-160 of 212) with videos related to

Sort By:
Pageof 22
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patientsMasayo Kagami, Keisuke Nagasaki, Rika Kosaki, et al.
Pediatric Transplantation|October 18, 2014
Two-step transplantation for primary hyperoxaluria: a winning strategy to prevent progression of systemic oxalosis in early onset renal insufficiency casesKengo Sasaki, Seisuke Sakamoto, Hajime Uchida, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2004
Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndromeRie Yoshida, Tomonobu Hasegawa, Yukihiro Hasegawa, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 9, 2013
Adult heights of 258 girls with turner syndrome on low dose of growth hormone therapy in JapanKeinosuke Fujita, Susumu Yokoya, Kenji Fujieda, et al.
Pediatric Transplantation|November 7, 2024
The Impact of Early Indication of Living Donor Liver Transplantation on the Outcomes of Patients With Propionic Acidemia: A Single-Center ExperienceToshimasa Nakao, Seisuke Sakamoto, Seiichi Shimizu, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision), , , et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 22, 2020
A nationwide questionnaire survey targeting Japanese pediatric endocrinologists regarding transitional care in childhood, adolescent, and young adult cancer survivorsYoko Miyoshi, Tohru Yorifuji, Chikako Shimizu, et al.
The Journal of Clinical Endocrinology and Metabolism|June 3, 2016
Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1bAkie Nakamura, Erika Hamaguchi, 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, 2013
Hepatocyte transplantation using a living donor reduced graft in a baby with ornithine transcarbamylase deficiency: a novel source of hepatocytesShin Enosawa, Reiko Horikawa, Akiko Yamamoto, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 24, 2015
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision), , , et al.
Pageof 22