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Frontiers in Endocrinology|February 27, 2023
Monitoring treatment in pediatric patients with 21-hydroxylase deficiencyTomoyo Itonaga, Yukihiro Hasegawa
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|October 11, 2021
Therapeutic needs from early childhood in four patients with 21-hydroxylase deficiency harboring the P30L mutation on one alleleTomoyo Itonaga, Kazuhisa Akiba, Yukihiro Hasegawa
Frontiers in Endocrinology|February 10, 2022
First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase DeficiencyTomoyo Itonaga, Masako Izawa, Takashi Hamajima, et al.
Scientific Reports|April 10, 2023
Long-term trends of pediatric type 1 diabetes incidence in Japan before and after the COVID-19 pandemicFumika Matsuda, Tomoyo Itonaga, Miwako Maeda, et al.
Molecular Genetics and Metabolism Reports|December 11, 2023
Asymptomatic 3-methylglutaconic aciduria type 1 detected by high C5-OH on newborn screeningTomoyo Itonaga, Miwako Maeda, Hiroshi Koga, et al.
Diabetology International|July 3, 2023
Diabetic lipemia as a predisposing state to acute pancreatitis: a case report and literature reviewYuka Hirakuni, Tomoyo Itonaga, Fumika Matsuda, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 19, 2021
A Japanese infant presenting with hypocalcemic seizures resulting from hypovitaminosis D induced by non-celiac gluten sensitivityNobuyuki Kawano, Tomoyo Itonaga, Manabu Tojigamori, et al.
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