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2,551 results for “Complications”
Pisgah Complicated Stamped Rimsherd (2094p1227)
**Pisgah Complicated Stamped rimsherd** Location: Warren Wilson site (31Bn29), Buncombe County, North Carolina. Period: Mississippian, Pisgah phase (AD 1000-1400). Material: ceramic. Dimensions: length, 58.8 mm; width, 36.4 mm; thickness, 10.6 mm. Notes: Catalog no. 2094p1227, North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Chris LaMack. Source: Objaverse 1.0 / Sketchfab
Qualla Complicated Stamped Jar Rim (2156p97)
**Qualla Complicated Stamped jar rim** Location: Birdtown Mound (31Sw7), Swain County, North Carolina.. Period: Mississippian, Qualla phase (AD 1400-1700). Material: ceramic. Dimensions: length, 144 mm; width, 85 mm; thickness, 9 mm. Notes: Catalog no. 2156p97, North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Maddie Ferrell. Source: Objaverse 1.0 / Sketchfab
Data of top 50 most cited articles about COVID-19 and the complications of COVID-19
<p><strong>Background</strong></p> <p>This bibliometric analysis examines the top 50 most-cited articles on COVID-19 complications, offering insights into the multifaceted impact of the virus. Since its emergence in Wuhan in December 2019, COVID-19 has evolved into a global health crisis, with over 770 million confirmed cases and 6.9 million deaths as of September 2023. Initially recognized as a respiratory illness causing pneumonia and ARDS, its diverse complications extend to cardiovascular, gastrointestinal, renal, hematological, neurological, endocrinological, ophthalmological, hepatobiliary, and dermatological systems.</p> <p><strong>Methods</strong></p> <p>Identifying the top 50 articles from a pool of 5940 in Scopus, the analysis spans November 2019 to July 2021, employing terms related to COVID-19 and complications. Rigorous review criteria excluded non-relevant studies, basic science research, and animal models. The authors independently reviewed articles, considering factors like title, citations, publication year, journal, impact factor, authors, study details, and patient demographics.</p> <p><strong>Results</strong></p> <p>The focus is primarily on 2020 publications (96%), with all articles being open-access. Leading journals include The Lancet, NEJM, and JAMA, with prominent contributions from Internal Medicine (46.9%) and Pulmonary Medicine (14.5%). China played a major role (34.9%), followed by France and Belgium. Clinical features were the primary study topic (68%), often utilizing retrospective designs (24%). Among 22,477 patients analyzed, 54.8% were male, with the most common age group being 26–65 years (63.2%). Complications affected 13.9% of patients, with a recovery rate of 57.8%.</p> <p><strong>Conclusion</strong></p> <p>Analyzing these top-cited articles offers clinicians and researchers a comprehensive, timely understanding of influential COVID-19 literature. This approach uncovers attributes contributing to high citations and provides authors with valuable insights for crafting impactful research. As a strategic tool, this analysis facilitates staying updated and making meaningful contributions to the dynamic field of COVID-19 research.</p>
Dataset : Acute kidney injury complicating critical forms of COVID-19: risk factors and prognostic impact
<p><span><span>We aimed to assess the incidence, risk factors and prognostic impact of AKI complicating critical forms of COVID-19. Thus we conducted a</span> retrospective descriptive case/control monocentric study conducted in a medical intensive care unit of a tertiary teaching hospital over a period of 18 months.</span></p>
Even short-term revegetation complicates soil food webs and strengths their links with ecosystem functions
<p>Degradation of dryland ecosystems is a worldwide problem caused by climate change and human activities. To restore these degraded ecosystems, governments have implemented projects that often include revegetation, but we still lack an understanding of how soil food webs and ecosystem functions are affected by revegetation. By conducting a large-scale revegetation experiment under two degradation intensities (low and high) on the Inner Mongolian degraded grassland, we tested the effects of revegetation on primary producers (plants), key components of soil food webs (bacteria, fungi, and nematodes), and ecosystem functions (soil C and N mineralization). After 4 years, revegetation greatly increased the biomass of plants and soil bacteria and fungi but had less effects on soil nematode functional groups. Revegetation increased vegetation and bacterial diversities and soil C and N mineralization rates, altered the structures of vegetation and soil microbial communities, but did not affect fungal or nematode diversity. The stronger effects of revegetation on plants, soil bacteria, soil fungi, and soil nematodes in plots with low degradation intensity than in plots with high degradation intensity indicated that future revegetation efforts should consider the degree of degradation. Revegetation also increased the interactions among plants, soil food webs, and ecosystem functions, indicating that the revegetation-induced changes in soil food webs could facilitate the recovery of soil nutrients and vegetation productivity in degraded grasslands. Synthesis and applications. Overall, the effects of revegetation were stronger on plants (primary producers) and soil microorganisms (intermediate trophic levels) than on soil nematodes (higher trophic levels), and even short-term revegetation increased the complexity of soil food webs and strengthened their relationships with soil functions in degraded grasslands. These results highlight the effects of restoration on multiple trophic levels in degraded drylands, and suggest that some aspects of plant-soil interactions in global drylands could be rapidly improved by appropriate restoration.</p>
FIGURE 24 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 24. Non-metric multidimensional (MDS) ordination of morphometric percentages (%TL) of recently revised Centrophorus species: C. granulosus (blue triangles), C. lesliei (purple diamonds), C. longipinnis (green squares) and C. uyato (red triangles). The samples in size class 1 for each species is distinguished by a dashed line. (A) two-dimensional plot; (B) threedimensional plot.
FIGURE 20 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 20. Distribution of Centrophorus uyato based on specimens examined, genetic tissue samples or validated literature records.
FIGURE 17 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 17. Left pectoral fin skeleton in ventral view (A) and pectoral girdle in lateral view (B) of Centrophorus uyato (CSIRO H 6310-04). Abbreviations: co, coracoid bar; fd, diazonal foramen; ms, mesopterygium; mt, metapterygium; mtx, metapterygial axis; pr, propterygium; rl, segmented radials consisting of proximal elements (pe, pale green), medial elements (pale yellow) and distal elements (de, pale purple); sc, scapula; *, distal separation between mesopterygium and metapterygium. Scale bar: 10 mm.
FIGURE 23 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 23. Colour variation in Centrophorus uyato (from Guallart, 1998): (A) female late-term embryo, 420 mm TL, found in the right uterus of (C) below; (B) juvenile female, 598 mm TL; (C) pregnant female, 978 mm TL; (D) adult male (var dark brown), 875 mm TL. Illustrations by Susana Rodríguez.
FIGURE 14 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 14. Variation in colour of adult male Centrophorus uyato from the Balearic Sea (Western Mediterranean): medium grey in top and bottom individuals, uniformly medium brown in middle individual.
FIGURE 15 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 15. Neurocranium of Centrophorus uyato (CSIRO H 6310-04, female). (A) dorsal view; (B) ventral view; (C) lateral view; (D) posterior view. Abbreviations: af, anterior fontanelle; ba, basal angle; bp, basal plate; btp, basitrabecular process; cp1, first cartilaginous process; cp2, second cartilaginous process; cr, cranial roof; csa, anterior semicircular canal; csl, lateral semicircular canal; csp, posterior semicircular canal; ec, ethmoidal canal; eec, ectethmoid chamber; ef, endolymphatic fossa; elf, endolymphatic foramen; ep, epiphysial pit; es, eye-stalk (base only); fca, foramen for carotid artery; fm, foramen magnum; foa, foramen for orbital artery; fopp, profundus canal; fops, series of foramina for superficial ophthalmic branch of trigeminal and facial nerves; hmf, hyomandibular facet; hmVII, foramen for hyomandibularis facialis; lra, lateral rostral appendage; mrp, median rostral prominence; ns, nasal capsule; oc, otic capsule; occ, occipital condyle; opp, opisthotic process; otc, otic crest; pcf, precerebral fossa; pecet, ectethmoid process; plf, perilymphatic foramen; poc, preorbital canal; pop, postorbital process; potp, prootic process; pow, preorbital wall; ppc, preorbital process; r, rostrum; rk, rostral keel; sec, subethmoid chamber; ser, subethmoidean ridge; snf, subnasal fenestra; soc, supraorbital crest; sphr, sphenopterotic ridge; II, optic foramen; III, oculomotor foramen; IV, trochlear foramen; V, VII, foramen prooticum; VI, abducens foramen; IX, foramen for glossopharyngeal nerve; X, vagus foramen; *, ridge at anterior of csa. Scale bar: 10 mm.
FIGURE 18 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 18. Left pelvic fin skeleton of Centrophorus uyato (CSIRO H 6503-04) in dorsal view. Abbreviations: abv, anterior pelvic basal; bpt, basipterygium; rl, segmented radials consisting of proximal elements (pe, pale green) and distal elements (de, pale purple); basipterygium elements (grey). Scale bar: 10 mm.
FIGURE 12 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 12. Pectoral fin of Centrophorus uyato in ventral view: (A); juvenile (BPS-0489, newborn male 470 mm TL); (B) adult (not retained, male 870 mm TL).
FIGURE 13 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 13. Right clasper of Centrophorus uyato in dorsal view (CSIRO H 6309-01, adult male 865 mm TL). Abbreviations: ap, apopyle; cg, clasper groove; hp, hypopyle; p2, pelvic fin; rh, rhipidion; td, dorsal terminal cartilage; t3, accessory terminal cartilage (spur); * thickened portion at attachment area of clasper and pelvic fin. Scale bar: 10 mm.
FIGURE 19 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 19. Clasper cartilages, right side, of Centrophorus uyato (CSIRO H 6309-02, adult male). Detail of terminal cartilages in (A) dorsal view; (B) ventral view. Abbreviations: ax, axial cartilage; rd, dorsal marginal cartilage; rv, ventral marginal cartilage; td, dorsal terminal cartilage; td2, dorsal terminal 2 cartilage; tv, ventral terminal cartilage; t3, accessory terminal cartilage (spur). Scale bars: 10 mm.
FIGURE 9 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 9. Lateral view of juvenile of Centrophorus uyato CSIRO H 7472-01, 440 mm TL juvenile male): (A) lateral view; (B) dorsal view.
FIGURE 10 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 10. Ventral view of the head of Centrophorus uyato: (A) juvenile (BPS-0489, newborn male 470 mm TL); (B) juvenile (BPS-0488, female 687 mm TL); (C) adult (MNHN-IC 2005-0169, male 892 mm TL).
FIGURE 7 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 7. Maximum Likelihood tree estimated under the General Time Reversible model (GTR) with model terms to accommodate both Invariant site (I) and Gamma Distributed rates (G). Bootstrap support values are shown from a separate ML bootstrap analysis. GenBank accession numbers are provided.
FIGURE 5 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 5. Lateral view of: (A) Dalatias nocturnus, original illustration from Rafinesque (1810); (B) preserved lectotype of Centrophorus bragancae (BMNH 1904.11.30.12, female 467 mm TL); (C) holotype of Centrophorus machiquensis (MMF 3767), original illustration from Maul (1955); (D) holotype (fresh) of Centrophorus zeehaani (CSIRO H 6628–05, adult male 893 mm TL).
FIGURE 8 in Revision of the genus Centrophorus (Squaliformes: Centrophoridae): Part 3-Redescription of Centrophorus uyato (Rafinesque) with a discussion of its complicated nomenclatural history
FIGURE 8. Lateral view of the adult neotype of Centrophorus uyato (BMNH 2021.10.4.1, adult male 983 mm TL; image flipped, right side shown).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.