Production of Prompt Charmonia in e+e- Annihilation at sqrt[s] ≈ 10.6 GeV

journal articl

＜論説＞延命医療・ケアの決定法制における争点の比較研究―韓国・日本・台湾の規範を中心として―

departmental bulletin pape

アタラシイ ヒカリエネルギー ヘンケンケイ ノ コウチク

video/mp4講演者所属: 大阪大学大学院工学研究科vide

Effects of Addition of Na and S to Alumina Catalyst for the Selective Reduction of Nitrogen Monoxide with Ethene in Excess Oxygen

journal articl

ヨーロッパにおける国境を越えた集団的権利保護

2010-03-25departmental bulletin pape

特集10 : 研究速報 : 閉鎖空間内の対流熱伝達シミュレーション : 低レイノルズ数型k-εモデルによる自然対流解析の試み

特集 乱流の数値シミュレーション（NST） その7departmental bulletin pape

Haplotypes and polyclonal infections detected in Th2R, Th3R and the repeat region.

Haplotypes and polyclonal infections detected in Th2R, Th3R and the repeat region.</p

Distribution of Th3R haplotypes across seasons, age groups, and clinical and non-clinical <i>Plasmodium falciparum</i> infections.

The prevalence of each unique Th3R haplotype that was present in at least 10% of all 454 reads of a given sample was calculated and stratified by the malaria transmission season in which they were collected, by three age groups (age≤5, age 6–10, and age≥11), and whether or not they were derived from samples that came from clinical vs. asymptomatic infections.</p

A Rare Case of a Solid Variant Aneurysmal Bone Cyst of the Medial Sphenoid Bone: Clinical Features, Diagnostic Points, and Treatment

A 5-year-old boy presented to our hospital with ptosis and an abnormal ocular position. Magnetic resonance imaging showed a well-defined mass measuring 20 mm in diameter in the medial sphenoid bone extending to the orbit and compressing the external ocular muscle. The patient underwent total surgical excision and was subsequently diagnosed with a solid variant of aneurysmal bone cyst via molecular integrated diagnosis. Solid variant of aneurysmal bone cyst is an extremely rare subtype of aneurysmal bone cyst, accounting for 0.2% of all primary bone tumors. It is characterized by the absence of a solid cystic component, which is difficult to diagnose via conventional hematoxylin and eosin staining. Molecular analyses revealed that this subtype is also characterized by the rearrangement of USP6 and the absence of the H3F3A mutation. This report discusses the clinical features of this extremely rare neoplastic lesion, the importance of an integrated diagnosis, and treatment options

Clinical, direct microscopic and Wood’s lamp examination features of <i>tinea capitis</i> lesions according to the identified dermatophyte species and non-dermatophyte filamentous fungus.

<p>Clinical, direct microscopic and Wood’s lamp examination features of <i>tinea capitis</i> lesions according to the identified dermatophyte species and non-dermatophyte filamentous fungus.</p