Search Results - "Itonaga, Tomoyo"

Long-term trends of pediatric type 1 diabetes incidence in Japan before and after the COVID-19 pandemic by Matsuda, Fumika, Itonaga, Tomoyo, Maeda, Miwako, Ihara, Kenji

“…Type 1 diabetes incidence has increased worldwide, although the long-term trends on pediatric type 1 diabetes in Japan remain elusive. To investigate the…”
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Monitoring treatment in pediatric patients with 21-hydroxylase deficiency by Itonaga, Tomoyo, Hasegawa, Yukihiro

“…21-hydroxylase deficiency (21-OHD) is the most common form of congenital adrenal hyperplasia. In most developed countries, newborn screening enables diagnosis…”
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Factors associated with low bone mineral density in Turner syndrome: a multicenter prospective observational study by Ikegawa, Kento, Koga, Eri, Itonaga, Tomoyo, Sakakibara, Hideya, Kawai, Masanobu, Hasegawa, Yukihiro

“…Turner syndrome (TS) is associated with a high risk of fracture due to low bone mineral density (BMD). While hypogonadism is known to play a role in decreasing…”
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Diabetic lipemia as a predisposing state to acute pancreatitis: a case report and literature review by Hirakuni, Yuka, Itonaga, Tomoyo, Matsuda, Fumika, Maeda, Miwako, Ihara, Kenji

“…Hypertriglyceridemia has been recognized as a common complication of diabetes ketoacidosis (DKA), whereas severe hypertriglyceridemia, also known as diabetic…”
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First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase Deficiency by Itonaga, Tomoyo, Izawa, Masako, Hamajima, Takashi, Hasegawa, Yukihiro

“…Biochemically monitoring 21-hydroxylase deficiency (21-OHD) is challenging. Serum/blood 17-hydroxyprogesterone (17OHP) measurements are normally used for this…”
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A retrospective multicenter study of bone mineral density in adolescents and adults with Turner syndrome in Japan by Itonaga, Tomoyo, Koga, Eri, Nishigaki, Satsuki, Kawai, Masanobu, Sakakibara, Hideya, Hasegawa, Yukihiro

“…Osteoporosis is one of the clinical features of women with Turner syndrome (TS). The reasons for low bone mineral density (BMD) and increased bone fragility…”
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Atypical food protein‐induced enterocolitis syndrome after vaccinations by Nishibayashi, Hayato, Itonaga, Tomoyo, Kuga, Shuji, Ohno, Takuro, Ihara, Kenji

“…Eight days later, poor activity with severe hypoalbuminemia (serum albumin level of 1.6 g/dL) with weight loss (5.9 kg) were detected by the primary…”
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A longitudinal ulcer due to Yersinia pseudotuberculosis infection in a girl by Hirahara, Shinnosuke, Itonaga, Tomoyo, Takeguchi, Masahiro, Suenobu, Souichi, Ihara, Kenji

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Asymptomatic 3-methylglutaconic aciduria type 1 detected by high C5-OH on newborn screening by Itonaga, Tomoyo, Maeda, Miwako, Koga, Hiroshi, Hasegawa, Yuki, Ihara, Kenji

“…3-Methylglutaconic aciduria type 1 (MGCA1) is an inborn error of leucine catabolism caused by pathogenic variants of the AUH gene. MGCA1 can be identified by…”
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Knowns and unknowns about congenital hypothyroidism: 2022 update by Itonaga, Tomoyo, Hasegawa, Yukihiro, Higuchi, Shinji, Satoh, Mari, Sawada, Hirotake, Shimura, Kazuhiro, Takahashi, Ikuko, Takubo, Noriyuki, Nagasaki, Keisuke

“…Several excellent guidelines and expert opinions on congenital hypothyroidism (CH) are currently available. Nonetheless, these guidelines do not address…”
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Therapeutic needs from early childhood in four patients with 21-hydroxylase deficiency harboring the P30L mutation on one allele by Itonaga, Tomoyo, Akiba, Kazuhisa, Hasegawa, Yukihiro

“…21-hydroxylase deficiency (21-OHD) is the most common type of congenital adrenal hyperplasia. Phenotypically, 21-OHD can be divided into classical and…”
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Hydrocortisone improved dexamethasone‐induced neuropsychological adverse effects by Oyake, Momoko, Itonaga, Tomoyo, Hirano, Naoki, Suenobu, Souichi, Ihara, Kenji

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An autopsy case of recurrent pneumothorax and peliosis-like intrapulmonary hematoma with X-linked myotubular myopathy by Yabe, Tomona, Itonaga, Tomoyo, Kuga, Shuji, Koga, Hiroshi, Kusaba, Takahiro, Nishida, Haruto, Daa, Tsutomu, Maeda, Tomoki, Ihara, Kenji

“…The typical non-muscle complications of long-surviving X-linked myotubular myopathy (XLMTM) include scoliosis, head deformity, macrocephaly, gastroesophageal…”
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Pubertal induction in Turner syndrome without gonadal function: A possibility of earlier, lower-dose estrogen therapy by Hasegawa, Yukihiro, Hasegawa, Tomonobu, Satoh, Mari, Ikegawa, Kento, Itonaga, Tomoyo, Mitani-Konno, Marie, Kawai, Masanobu

“…Delayed and absent puberty and infertility in Turner syndrome (TS) are caused by primary hypogonadism. A majority of patients with TS who are followed at…”
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Onasemnogene Abeparvovec Treatment after Nusinersen in an Infant with Spinal Muscular Atrophy Type 1 by Nanri, Daiki, Yuge, Kotaro, Goto, Kohei, Kimura, Takuro, Yae, Yukako, Mizuochi, Tatsuki, Sato, Ryosuke, Itonaga, Tomoyo, Maeda, Tomoki, Yamashita, Yushiro

“…Until recently, the treatment of spinal muscular atrophy (SMA) was limited to symptomatic treatment with no cure. Three innovative drugs, nusinersen,…”
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Levothyroxine Dosage as Predictor of Permanent and Transient Congenital Hypothyroidism: A Multicenter Retrospective Study in Japan by Itonaga, Tomoyo, Higuchi, Shinji, Shimura, Kazuhiro, Nagasaki, Keisuke, Satoh, Mari, Takubo, Noriyuki, Takahashi, Ikuko, Sawada, Hirotake, Hasegawa, Yukihiro

“…Congenital hypothyroidism (CH) can be divided into 2 types, transient CH (T-CH) and permanent CH (P-CH), depending on the requirement of levothyroxine (LT4)…”
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A Seven-Year-Old Girl With Dysphagia Due to Fear of Swallowing: A Favorable Outcome With Cognitive Behavioral Therapy Using an Anxiety Hierarchy Chart by Etoh, Mika, Itonaga, Tomoyo, Oguri, Saori, Kiyota, Akio, Ihara, Kenji

“…Avoidant/restrictive food intake disorder (ARFID) is an eating disorder characterized by avoidance and aversion to food and eating. Food restriction is not due…”
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Ultra-low-dose estrogen therapy for female hypogonadism by Hasegawa, Yukihiro, Itonaga, Tomoyo, Ikegawa, Kento, Nishigaki, Satsuki, Kawai, Masanobu, Koga, Eri, Sakakibara, Hideya, Ross, Judith L.

“…In females, endogenous estrogen secretion increases gradually before pubertal development. The benefits of low-dose estrogen therapy in patients with Turner…”
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PTPN11 and FLNA variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features by Muranishi, Yuki, Itonaga, Tomoyo, Ihara, Kenji, Katoh-Fukui, Yuko, Tamaoka, Satoshi, Hattori, Atsushi, Kon, Masafumi, Shinohara, Nobuo, Fukami, Maki

“…Noonan syndrome is a congenital disorder characterized by distinctive facial appearance, congenital heart defects, short stature, and skeletal dysplasia…”
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A Japanese infant presenting with hypocalcemic seizures resulting from hypovitaminosis D induced by non-celiac gluten sensitivity by Kawano, Nobuyuki, Itonaga, Tomoyo, Tojigamori, Manabu, Daa, Tsutomu, Ihara, Kenji

“…Vitamin D deficiency is a major cause of hypocalcemic seizures in infants. Chronic enteropathy can cause both malnutrition and vitamin deficiency disorders,…”
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