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552 results for “Literature review”
Systematic Literature Review - Selected Articles Data Extraction
<p>The files included are the following:</p> <p>- CSV with the raw data extracted from abstract + full-text review from the selected articles.</p> <p>- CSV with normalized data according to the article.</p> <p> </p>
Visual system involvement in GFAP astrocytopathy: two case reports and a systematic literature review
<p>Background and Objectives: Glial fibrillary acidic protein (GFAP) antibodies can associate with an astrocytopathy often presenting as a meningoencephalitis. Visual involvement has been reported, but scarcely defined. We describe two cases of GFAP astrocytopathy with predominant visual symptoms and present a systematic review of the literature. Methods: We describe two patients with GFAP astrocytopathy from our neurology department. We performed a systematic review of the literature according to PRISMA guidelines, including all patients with this disease and available clinical data, focusing on visual involvement. Results: Patient 1 presented with bilateral optic disc edema and severe sudden bilateral loss of vision poorly responsive to therapy. Patient 2 showed bilateral optic disc edema, headache, and mild visual loss with complete recovery after steroids. We screened 275 records and included 84 papers (62 case reports and 22 case series) for a total of 592 patients. Visual involvement was reported in 149/592 (25%), with either clinical symptoms, or paraclinical test-restricted abnormalities. Bilateral optic disc edema was found in 80/159 (50%) of patients investigated with fundoscopy, among which 49/80 (61%) were asymptomatic. One hundred (100/592, 17%) reported visual symptoms, often described as blurred vision or transient visual obscurations. Optic neuritis was rare and diagnosed in only 6% of all patients with GFAP astrocytopathy, often without consistent clinical and paraclinical evidence to support the diagnosis. Four patients (including patient 1) manifested a severe, bilateral optic neuritis with poor treatment response. In patients with follow-up information, a relapsing disease course was more frequently observed in those with vs without visual involvement (35% vs 11%, p=0.0035, OR 3.6 [CI 1.44 - 8.88]). Discussion: Visual system involvement in GFAP astrocytopathy is common and heterogeneous, ranging from asymptomatic bilateral optic disc edema to severe bilateral loss of vision, but optic neuritis is rare. GFAP CSF antibody testing should be considered in patients with encephalitis/meningoencephalitis or myelitis and bilateral optic disc edema, even without visual symptoms, and in patients with severe bilateral optic neuritis, especially when AQP4 antibodies are negative. Visual symptoms might associate with a higher relapse risk and help to identify patients which may require chronic immunosuppression.</p>
Visual system involvement in GFAP astrocytopathy: two case reports and a systematic literature review
<p>The database contains information regarding patients with GFAP astrocytopathy reported in the literature included in the revew, including demographic, clinical presentation and course, neuroradiological data, laboratory data, treatment and outcome data, paraclinical test results.</p>
A global systematic literature review of ecosystem services in reef environments
<p>Data from a systematic review about ecosystem services in reef environments. </p>
Cognitive function in DMD carriers: personal case series and literature review
<p>Introduction: This database includes the raw data linked with the paper “Cognitive function in DMD carriers: personal case series and literature review” published on “Acta Myologica”. Aim: This study aimed to investigate the cognitive involvement in a cohort of DMD carriers.</p> <p>Methods: Our case series consisted of 22 carrier patients from two different centers (IRCCS Mondino, Pa- via and Policlinico Gemelli, Rome), for whom we retrospectively collected cognitive, clinical and genetic data.</p> <p>Results: We found that the average IQ of DMD carriers was lower (74; very low) than the average score on normal curve (100 as average standard score). Furthermore, about 50% of them fell in the “extremely low IQ” range, compared with 2-3% of general population. A higher incidence of intellectual disability was confirmed in symptomatic DMD carriers (mean IQ 66; extremely low) from the IRCCS Mondino, but not for the asymptomatic ones (mean IQ 99; average), when compared to the general population.</p>
Central hypogonadism in Klinefelter syndrome: report of two cases and review of the literature, Table
<p><strong>Review of previously published reports of hypogonadotropic hypogonadism in Klinefelter syndrome (KS).</strong></p> <p>Ys, years. N/A, not assessed. HH, hypogonadotropic hypogonadism. T, total testosterone. LH, luteinizing hormone. FSH, follicle stimulating hormone. LHRH, LH releasing hormone. hCG, human chorionic gonadotropin. GH, growth hormone. ACTH, adrenocorticotropin. TSH, thyroid stimulating hormone. CHH, congenital hypogonadotropic hypogonadism.</p> <p>Table of <a href="https://doi.org/10.1007/S40618-020-01324-3"><strong>10.1007/S40618-020-01324-3</strong></a></p>
Collection of primary literature pdfs from the Goldberg reviews
<p>These are the archive copies of all currently crawled pdf files from the Goldberg reviews.</p>
Chapter 5 Identifying Adaptive Algorithms for Increasing Comparative Judgment Efficiency: A Systematic Literature Review
<p>This is a taxonomy of adaptive algorithms as a supplementary file with the article "Identifying Adaptive Algorithms for Increasing Comparative Judgment Efficiency: A Systematic Literature Review" and Chapter 5, with the same title, of the dissertation "Beyond a Mere Rank Order: The Method, the Reliability and the Efficiency of Comparative Judgment" by San Verhavert (University of Antwerp).</p>
Preventive measures against the development of white spot lesions during fixed orthodontic treatment: a systematic review of the literature and meta-analysis
<p>Datasets for all analyses done in the study.</p>
Which are the most frequently involved peripheral joints in calcium pyrophosphate crystal deposition at imaging? A Systematic Literature Review and meta-analysis by the OMERACT Ultrasound – CPPD subgroup
<p><strong>Objectives</strong>: To identify the prevalence of calcium pyrophosphate crystal deposition (CPPD) using ultrasound and conventional radiology at peripheral joints in patients with suspected or definite CPPD.</p> <p><strong>Methods: </strong>A systematic literature search was performed in PubMed and Embase using pre-defined search strategies from inception to April 2021 to identify studies that evaluated conventional radiology and ultrasound in detecting CPPD at peripheral joints, including definite or suspected CPPD [Research question 1 (RQ1) and Research Question 2 (RQ2), respectively]. For the meta-analysis, the first, second, and third sub-analysis included studies with the knee, and knee or wrist as the index joint for CPPD (without restrictions on the reference standard) and synovial fluid analysis or histology as a reference standard (without restrictions on the index joint), respectively.</p> <p><strong>Results: </strong>One-thousand eight hundred and twenty-seven manuscripts were identified, of which 94 articles were finally included. Twenty-two and seventy-two papers were included in RQ1 and RQ2, respectively. The knee had the highest prevalence for RQ1 and RQ2 by both conventional radiology and ultrasound, followed by the wrist with the highest prevalence for RQ1. The hand had the lowest CPPD prevalence. The third sub-analysis showed a higher CPPD prevalence on ultrasound than conventional radiology at the knee (only data available).</p> <p><strong>Conclusion: </strong>Among all peripheral joints, the knees and wrists could be regarded as the target joints for CPPD detection by imaging. Furthermore, ultrasound seems to detect a higher number of calcium pyrophosphate deposits than conventional radiology, even when using a more restrictive reference standard.</p>
dataset related to submitted article "Novel HSPG2 gene mutation causing Schwartz-Jampel syndrome in a Moroccan family and review of the literature"
<p>Next Generation Sequencing, real-time, sequensing cDNA</p>
Defining Secure DevOps and the Missing Global Dimension: A Multi-vocal Literature Review
<p>Data and associated materials</p>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.