266) Clinical evaluation included pocket depth, |
267) Our findings suggest that clinical evaluation of aqueous flare is su |
268) Sterility measures were applied for clinical evaluation. |
269) tiating cells and the benefit for further clinical evaluation. |
270) ve to pathobiological modeling as well as clinical management for oral mucositis cau |
271) The daily clinical management has benefited by the i |
272) s well-tolerated and may be useful in the clinical management of bone-invasive felin |
273) e subsequent physiologic consequences and clinical management. |
274) rt of embryos on day 3 resulted in better clinical outcomes compared with cryopreser |
275) nuary and 31 December of 2010 to evaluate clinical outcomes that occur when a new In |
276) veness of various debridement methods and clinical outcomes to help inform clinician |
277) king and impulsivity may markedly improve clinical outcomes. |
278) in disease (LSD) in Jordan and associated clinical signs, complications and prelimin |
279) Signalment, type and duration of clinical signs, metastasis site, pathology |
280) ient animals by monitoring development of clinical signs, testing of blood for the p |
281) ion and decreased body weight were common clinical signs, while mastitis and myiasis |
282) bleeding on probing, probing depth (PD), clinical attachment level (CAL), and gingi |
283) Probing depth, clinical attachment level, and keratinized |
284) idual pockets (pocket depth (PD) ≥5 mm, clinical attachment loss ≥2 mm, and blee |
285) and its relation to age of disease onset, clinical course, and response to therapy. |
286) ive" and "executive" parallel the disease clinical course, being at the same time re |
287) r stratification by age of disease onset, clinical course, or response to therapy. |
288) cute pulmonary edema was suspected on the clinical examination, chest radiography, b |
289) to fibrogenic dust, who were subjected to clinical examination, pulmonary function t |
290) iagnosis is typically made by history and clinical examination, while ancillary test |
291) with HCV infection, as well as share our clinical experience in diagnosing and mana |
292) a selective literature search and our own clinical experience is to characterise the |
293) preclinical studies, we report our first clinical experience with transcatheter clo |
294) Setting : Clinical information and DNA samples were |
295) ly accepted vocabulary standards into our clinical information systems, physiotherap |
296) 7 index were performed in all samples and clinical information was obtained by a fol |
297) t, which may explain the heterogeneity in clinical manifestations and symptom severi |
298) rioration model, which are similar to the clinical manifestations of DTI deteriorati |
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