Results 161 to 170 of about 38,108 (302)

Reduced Muscular Carnosine in Proximal Myotonic Myopathy—A Pilot 1H‐MRS Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Myotonic dystrophy type 2 (proximal myotonic myopathy, PROMM) is a progressive multisystem disorder with muscular symptoms (proximal weakness, pain, myotonia) and systemic manifestations such as diabetes mellitus, cataracts, and cardiac arrhythmias.
Alexander Gussew   +11 more
wiley   +1 more source

ITER breeding blanket module design & analysis

open access: yesITER breeding blanket module design & analysis
トリチウム増殖材と中性子増倍材をいずれも微小球ペブル状として充填する設計となっているITER増殖ブランケットに対し、とくにペブル充填層の熱・機械特性に着目して汎用熱・構造解析コードABAQUSの特殊計算オプションを使用した熱・機械解析を実施した。また、耐高熱負荷が問題となる第一壁について、Beアーマとステンレス鋼構造材の接合部における熱応力履歴を弾塑性解析により求めると共に、これに基づいて、アーマ/構造材接合部における強度評価方法について検討した。さらに、増殖ブランケット・モジュールの製作に関し、第一壁及び冷却パネル、増殖材充填部等の各構成要素を個々に製作し、それらを組み合わせることを基本として各構成要素の製作方法及び全体組立手順を検討した。
openaire  

Association of Corticospinal Tract Asymmetry With Ambulatory Ability After Intracerebral Hemorrhage

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Ambulatory ability after intracerebral hemorrhage (ICH) is important to patients. We tested whether asymmetry between ipsi‐ and contra‐lesional corticospinal tracts (CSTs) assessed by diffusion tensor imaging (DTI) is associated with post‐ICH ambulation.
Yasmin N. Aziz   +25 more
wiley   +1 more source

Liquid metals power advanced nuclear energy systems. [PDF]

open access: yesInnovation (Camb)
Zhang L, Deng C, Ji X, Liu X.
europepmc   +1 more source

Tritium breeding capability of heliotron-H fusion reactor blankets. [PDF]

open access: yesJournal of Nuclear Science and Technology, 1982
Hideki NAKASHIMA   +2 more
openaire   +1 more source

Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz   +3 more
wiley   +1 more source

Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky   +8 more
wiley   +1 more source

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