Search Results - "Narumi, Hiroko"
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1
Successful control of radicular pain in a pediatric patient with Guillain–Barré syndrome
Published in Brain & development (Tokyo. 1979) (01-10-2015)“…Abstract A 10-year-old boy was diagnosed as having the axonal form of Guillain–Barré syndrome (GBS). The patient noticed progressive weakness of the lower legs…”
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2
Time-Course Evaluation of Body Mass Index in Japanese Children With Obstructive Sleep Apnea Syndrome After Adenotonsillectomy: A Three-Years Follow-Up Study
Published in Frontiers in pediatrics (04-02-2020)“…Delayed physical growth is a common complication of pediatric obstructive sleep apnea syndrome (OSAS). Adenotonsillectomy (AT) is the first-line treatment for…”
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3
Clitoral preputial edema can be mistaken for clitoromegaly: a clinical analysis of ten cases
Published in Frontiers in endocrinology (Lausanne) (07-07-2023)“…We herein reported ten, female neonates with transient clitoral preputial edema, which was mistaken for clitoromegaly. Although it is well known that the…”
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4
Non-androgen secreting adrenocortical carcinoma in preadolescence: a case report and literature review
Published in Journal of pediatric endocrinology & metabolism : JPEM (01-11-2016)“…Adrenocortical carcinoma (ACC) is a rare malignancy in childhood. Affected children with ACC mostly present with virilization, but not the pure form of…”
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A novel de novo mutation of β-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy
Published in Journal of genetics (01-08-2014)Get full text
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A novel de novo mutation of [beta]-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy
Published in Journal of genetics (01-08-2014)“…Hypertrophic cardiomyopathy (HCM) is characterized by thickening of left ventricle (LV), especially the interventricular septum (IVS), and diastolic…”
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Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects
Published in The journal of clinical endocrinology and metabolism (13-08-2024)“…Abstract Context Thyroglobulin (Tg), encoded by TG, is essential for thyroid hormone synthesis. TG defects result in congenital hypothyroidism (CH). Most…”
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Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects
Published in The journal of clinical endocrinology and metabolism (19-02-2024)“…Thyroglobulin (Tg), encoded by TG, is essential for thyroid hormone synthesis. TG defects result in congenital hypothyroidism (CH). Most reported patients were…”
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