[HTML][HTML] Regulation of Serum Sodium Levels during Chemotherapy Using Selective Arginine Vasopressin V2-Receptor Antagonist Tolvaptan in a Four-Year-Old Girl …

S Hiroshima, H Nyuzuki, S Sasaki, Y Ogawa… - Children, 2021 - mdpi.com
There are limited reports on the use of tolvaptan for syndrome of inappropriate antidiuretic
hormone secretion (SIADH) in children. Managing serum sodium levels in SIADH patients …

[HTML][HTML] Infantile-Onset Isolated Neurohypophyseal Langerhans Cell Histiocytosis with Central Diabetes Insipidus: A Case Report

M Tani, S Hiroshima, H Sato, K Sawano, Y Ogawa… - Children, 2022 - mdpi.com
Central diabetes insipidus (CDI) is a rare disease in children and has a variety of etiologies.
The major causes of CDI with pituitary stalk thickening (PST) are germinoma, Langerhans …

[HTML][HTML] Re-evaluation of the prevalence of permanent congenital hypothyroidism in Niigata, Japan: a retrospective study

K Nagasaki, H Sato, S Sasaki, H Nyuzuki… - International Journal of …, 2021 - mdpi.com
Although newborn screening (NBS) for congenital hypothyroidism (CH) in Japan started
more than 40 years ago, the prevalence of CH remains unclear. Prevalence estimations …

[HTML][HTML] Diagnosis of Chromosome 15q-Terminal Deletion Syndrome through Elevated Fasting Serum Growth Hormone Levels

M Ono, M Tanaka, S Hiroshima, K Sawano, Y Ogawa… - Endocrines, 2022 - mdpi.com
Chromosome 15q26-qter deletion syndrome is a rare disease that causes prenatal and
postnatal growth retardation, microcephaly, developmental delay, and congenital heart …

A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings.

T Onuki, N Shibata, S Hiroshima… - Congenital …, 2022 - search.ebscohost.com
The Indian hedgehog gene (I IHH i; NM 002181.4) is mapped on chromosome 2q35-36 and
encodes the IHH protein belonging to the Hedgehog protein family. As is well known …

Graves' disease in children: an enlarged goitre causes severe tracheal stenosis

S Hiroshima, Y Ueki, K Yamazaki… - BMJ Case …, 2021 - search.proquest.com
Since the disease onset, he had been reporting discomfort during swallowing owing to the
enlarged goitre. The CT scan of the neck showed that the minimum tracheal diameter was 3 …

Two cases of 22q11. 2 deletion syndrome with decreased serum calcium during recovery following thyrotoxicosis.

S Hiroshima, C Taniguchi, M Inoue… - Congenital …, 2022 - search.ebscohost.com
In six cases of Graves' disease, hypocalcemia developed approximately 1-5 months after
antithyroid drug initiation, and in patient 2, serum Ca levels began to decline even when FT4 …

A Study on New Mothers Diagnosed with Inborn Errors of Metabolism Via Positive Newborn Mass Screening in Their Newborns

T Onuki, H Nyuzuki, S Hiroshima, K Sawano… - Available at SSRN … - papers.ssrn.com
There exist some reports of new mothers being diagnosed with inborn errors of metabolism
(IEM) upon positive newborn mass screening (NBS) in their newborn. Such IEM patients are …

[HTML][HTML] A Study of Maternal Patients Diagnosed with Inborn Errors of Metabolism Due to Positive Newborn Mass Screening in Their Newborns

T Onuki, S Hiroshima, K Sawano, N Shibata, Y Ogawa… - Children, 2023 - mdpi.com
Background: There are reports of mothers being diagnosed with inborn errors of metabolism
(IEM) via positive newborn screening (NBS) of their newborns. Mothers with IEM are often …

Growth Hormone Injection Log Analysis with Electronic Injection Device for Qualifying Adherence to Low-Irritant Formulation and Exploring Influential Factors on …

K Takasawa, H Mabe, F Nagamatsu… - Patient preference …, 2023 - Taylor & Francis
Introduction Although the treatment success of long-term growth hormone therapy (GHT) is
dependent on maintaining patients' adherence to treatment, marked variations in adherence …