Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tokuo Mukai

Showing results (1-10 of 32) with videos related to

Pageof 4
Sort By:
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 13, 2006
[Kallmann syndrome]Kenji Fujieda, Tokuo Mukai
Nihon Rinsho. Japanese Journal of Clinical Medicine|February 19, 2004
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency]Kenji Fujieda, Tokuo Mukai
Pediatrics International : Official Journal of the Japan Pediatric Society|May 8, 2009
Prevalence and risk factors of vitamin D deficiency rickets in Hokkaido, JapanKumihiro Matsuo, Tokuo Mukai, Shigeru Suzuki, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 3, 2011
Patient reports: Two novel frameshift mutations in the SOX9 gene in two patients with campomelic dysplasia who showed long-term survivalToshio Okamoto, Eiki Nakamura, Ken Nagaya, et al.
The Journal of Clinical Endocrinology and Metabolism|July 20, 2007
Molecular basis of neonatal diabetes in Japanese patientsShigeru Suzuki, Yoshio Makita, Tokuo Mukai, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 29, 2003
Molecular pathogenesis of lipoid adrenal hyperplasia and adrenal hypoplasia congenitaKenji Fujieda, Koji Okuhara, Shuji Abe, et al.
Diabetologia|May 26, 2020
Sufficient increment of sulfonylurea without reintroduction of insulin ameliorates pubertal deterioration of glycaemic control in KCNJ11 neonatal diabetes treated with long-term sulfonylureaShigeru Suzuki, Tokuo Mukai, Takahide Kokumai, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 31, 2013
A Case of Vitamin D Deficiency without Elevation of Serum Alkaline Phosphatase in a Carrier of HypophosphatasiaKumihiro Matsuo, Tokuo Mukai, Akiko Furuya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 12, 2016
High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidismKumihiro Matsuo, Yusuke Tanahashi, Tokuo Mukai, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 19, 2022
Early Diagnosis of Wolfram Syndrome by Ophthalmologic Screening in a Patient with Type 1B Diabetes Mellitus: A Case ReportTakahide Kokumai, Shigeru Suzuki, Noriko Nishikawa, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 13, 2006
[Kallmann syndrome]Kenji Fujieda, Tokuo Mukai
Nihon Rinsho. Japanese Journal of Clinical Medicine|February 19, 2004
[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency]Kenji Fujieda, Tokuo Mukai
Pediatrics International : Official Journal of the Japan Pediatric Society|May 8, 2009
Prevalence and risk factors of vitamin D deficiency rickets in Hokkaido, JapanKumihiro Matsuo, Tokuo Mukai, Shigeru Suzuki, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 3, 2011
Patient reports: Two novel frameshift mutations in the SOX9 gene in two patients with campomelic dysplasia who showed long-term survivalToshio Okamoto, Eiki Nakamura, Ken Nagaya, et al.
The Journal of Clinical Endocrinology and Metabolism|July 20, 2007
Molecular basis of neonatal diabetes in Japanese patientsShigeru Suzuki, Yoshio Makita, Tokuo Mukai, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 29, 2003
Molecular pathogenesis of lipoid adrenal hyperplasia and adrenal hypoplasia congenitaKenji Fujieda, Koji Okuhara, Shuji Abe, et al.
Diabetologia|May 26, 2020
Sufficient increment of sulfonylurea without reintroduction of insulin ameliorates pubertal deterioration of glycaemic control in KCNJ11 neonatal diabetes treated with long-term sulfonylureaShigeru Suzuki, Tokuo Mukai, Takahide Kokumai, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 31, 2013
A Case of Vitamin D Deficiency without Elevation of Serum Alkaline Phosphatase in a Carrier of HypophosphatasiaKumihiro Matsuo, Tokuo Mukai, Akiko Furuya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 12, 2016
High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidismKumihiro Matsuo, Yusuke Tanahashi, Tokuo Mukai, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 19, 2022
Early Diagnosis of Wolfram Syndrome by Ophthalmologic Screening in a Patient with Type 1B Diabetes Mellitus: A Case ReportTakahide Kokumai, Shigeru Suzuki, Noriko Nishikawa, et al.
Pageof 4