Abstract P-380
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چکیده
منابع مشابه
P 380 Colorimetric analysis of the retinal pigmentation
Progrlsive cone dystroph!, ((:OI)), cone-rod dystrophy (CRD), choroidereruia (CHD) and rethdlis p@nentosa are fouur retinal progressive diwnl+rs which can he inherited iu a X linked fasbioo. We present 13 families afktd with ooe of tbes:r 4 disoredr;. We bare studied 16 arfecti men aurl 30 puaible feumle carriers. A completr ophtiilmic exploratiou a115 ILRG resting baoe hen done in every cxx. I...
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The paper presents an application of the Skyhook control of suspension MR dampers in a vehicular vibration control system. Experiments were conducted using an ATV (all-terrain vehicle) traversing a test route. The system elements were analyzed and calibrated paying special attention to the space orientation of sensors and MR dampers. Orientation data and inversed Bingham model, which maps dynam...
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O steoporosis is a systemic disorder characterized by microarchitectural deterioration of bone and increased susceptibility to fracture. Although osteoporosis can occur in men, it is principally a disease of women, who account for 80% of such cases and in whom osteoporosis (together with heart disease and cancer) is one of the three most common medical conditions.1-3 According to the National O...
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Background: A school’s learning environment is believed to influence academic performance yet few studies have evaluated this association controlling for prior academic ability, an important factor since students who do well in school tend to rate their school’s environment more highly than students who are less academically strong. Aim: To evaluate the effect of student perception of the learn...
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Ion channel dysfunction causes a range of neurological disorders by altering transmembrane ion fluxes, neuronal or muscle excitability, and neurotransmitter release. Genetic neuronal channelopathies affecting peripheral axons provide a unique opportunity to examine the impact of dysfunction of a single channel subtype in detail in vivo. Episodic ataxia type 2 is caused by mutations in CACNA1A, ...
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ژورنال
عنوان ژورنال: Pediatric Critical Care Medicine
سال: 2018
ISSN: 1529-7535
DOI: 10.1097/01.pcc.0000537837.89675.d1