Publications by authors named "H Saitou"

Osteogenesis imperfecta (OI) is an inheritable skeletal disorder characterized by bone fragility often caused by pathogenic variants in the COL1A1 gene. Current OI mouse models with a glycine substitution in Col1a1 exhibit excessive severity, thereby limiting long-term pathophysiological analysis and drug effect assessments. To address this limitation, we constructed a novel OI mouse model mimicking a patient with OI type III.

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Recently, a novel wireless flat-panel detector with auto-exposure control has become available. This study aimed to elucidate the potential advantages of the new detector over conventional detectors through a comprehensive analysis of the physical image quality characteristics. Measurements were conducted on two models: new (720C) and conventional (710C) versions; this assessment was performed by assuming the beam quality for bedside chest radiography, utilizing a portable device for X-ray exposure.

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Postmortem imaging, particularly unenhanced postmortem computed tomography (PMCT), has been increasingly utilized for pathological or judicial examination as a substitute for conventional autopsy, to compensate very low autopsy rates. While unenhanced PMCT has a limitation in diagnosing acute coronary syndromes, the fat attenuation index (FAI) which is a novel imaging biomarker measured by clinical coronary CT angiography (CCTA), has been known to noninvasively detect coronary artery inflammation. We investigated the postmortem diagnostic usefulness of perivascular FAI measured by CCTA in a 61-year-old male who died suddenly after chest pain.

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Objective: An accurate measurement of x-ray beams is expected to reduce the uncertainties associated with estimating radiation risk to patients in clinical settings. To perform assessment tasks based on the readings of a solid-state detector (SSD) using semiconductor technology, the characteristics of the detector should be elucidated. In this study, we evaluated the measurement accuracy of a new SSD under diagnostic x-ray beam conditions in terms of air kerma, tube voltage, and half-value layer (HVL).

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Article Synopsis
  • Achondroplasia (ACH) is a genetic condition leading to short stature and distinctive physical features, with a high complication rate observed in young patients.
  • A study reviewing medical records of Japanese children with ACH under 5 years highlighted that 89.2% had complications, and a majority required surgical interventions.
  • Growth hormone treatment initiated at age 3 resulted in significant height increases compared to untreated patients, emphasizing the importance of early diagnosis and monitoring for effective management.
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