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1 uminescence emission measurements along with postmortem examination.
2 n Aging-Reagan criteria following a standard postmortem examination.
3 survival of dopamine neurons was observed at postmortem examination.
4 a at risk, and infarct size were measured at postmortem examination.
5 pa uptake on positron-emission tomography or postmortem examination.
6 a cohort of newly diagnosed patients and by postmortem examination.
7 One of these two kidneys was small at postmortem examination.
8 most consistent with an embolic etiology on postmortem examination.
9 is large and confirms the importance of the postmortem examination.
10 variant of Alzheimer's disease who underwent postmortem examination.
11 using positron emission tomography (PET) and postmortem examination.
12 ably present in the lung and other organs at postmortem examination.
13 o have coronary artery disease identified on postmortem examination.
14 of the most reliable alterations observed at postmortem examination.
15 from radiologically confirmed pneumonia and postmortem examinations.
16 ues might provide an alternative approach to postmortem examinations.
17 ethods: Tissue was acquired from 11 detailed postmortem examinations.
18 268 [52.3%; 95% CI, 47.9%-56.7%]), perinatal postmortem examination (161 [31.4%; 95% CI, 27.5%-35.7%]
21 a/COVID-19 respiratory failure who underwent postmortem examination and/or tracheobronchial biopsy du
23 that considered the time-of-death interval, postmortem examination, and reliability of the gestation
25 0 days post-MI (43% versus 22%; P=0.04), and postmortem examination confirmed cardiac rupture as the
27 us was born at term and euthanized on day 3: postmortem examination confirmed the patency of the sten
31 nexplained death (19.5%) was the most common postmortem examination finding, followed by idiopathic l
37 8 years and lived for 105 months, underwent postmortem examination, including neuropathological exam
38 H relative to those of healthy controls upon postmortem examination, it remains controversial whether
39 ive tissue sampling (MITS) is a standardized postmortem examination method that holds promise for use
44 ption of individuals with genetic mutations, postmortem examination of brain tissue remains the only
53 here have been no reports on the findings of postmortem examination of the brain in treated patients
57 012, through November 11, 2014, we conducted postmortem examination of the eyes of 23 infants and chi
59 hilic Muller cell foot processes swelling in postmortem examination of young infant eyes, a potential
61 be distinguished from Alzheimer's disease by postmortem examination or by future in vivo measurements
71 asive tissue sampling (MITS) is a simplified postmortem examination technique that has shown to be an
72 ete diagnostic autopsy, is a pathology-based postmortem examination that has been validated in low- a
76 rdial tissue blocks obtained at the original postmortem examination were the source of deoxyribonucle
78 he patient who survived 105 months underwent postmortem examination which confirmed the diagnosis of
79 ases, substances were identified in serum at postmortem examination without evidence of drug overdose