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199
datasets available to search
ShareScore release 0.9.0
Dataset results
199 results for “CASE REPORT”
Diagnosis and Clinical Presentation of Iliac Graft-Enteric Fistula: A Case Report
ClinicalTrials.gov study NCT06553105. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Two Cases of Pulmonary Cysticercosis Manifesting as Pleural Effusion: Case Report and Literature Review
ClinicalTrials.gov study NCT05010811. IPD Sharing: NO. Countries: 0. Publications: 0.
Carpal Tunnel Syndrome: Case Reports and Analysis - Ultrasound Imaging and Pathomechanics of Median Nerve Compression
ClinicalTrials.gov study NCT00987571. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Impact of Real-time MIC (Minimum Inhibitory Concentration) Reporting (<6 Hours) on β-lactam Prescription in Cases of Gram-negative Bacilli Bacteremia in ICU Patients in Real-life Settings
ClinicalTrials.gov study NCT07202377. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Case Report of Endometrioma in Layers of Broad Ligament.
ClinicalTrials.gov study NCT02513953. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Report 2 Cases of Massive Incarceration Necrosis Rectal Prolapse Are Successfully Treated With Altemeier's Procedure
ClinicalTrials.gov study NCT03643393. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
Multiple chromoanasynthesis in a rare case of sporadic renal leiomyosarcoma: case report
GEO Series GSE151766. Homo sapiens. 1 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array; SNP genotyping by SNP array.
ALK-TPM3 rearrangement in adult renal cell carcinoma: report of a novel case showing misleading TFE3 expression and loss of chromosome 3 and literature review
GEO Series GSE96980. Homo sapiens. 1 samples. Type: Genome variation profiling by genome tiling array.
Single-cell transcriptome sequencing provides insight into multiple chemotherapy resistance in a patient with refractory DLBCL: a case report
GEO Series GSE244622. Homo sapiens. 1 samples. Type: Expression profiling by high throughput sequencing.
Drug-interaction annotations over full text articles reporting on clinical studies reports or case reports
<p>Drug interaction annotations over full text reports. These annotations were done as part of the National Library of Medicine funded research project "Addressing gaps in clinically useful evidence on drug-drug interactions" (R01LM011838)</p>
Hypodiploidy in a pediatric patient of T-cell acute lymphoblastic leukemia: a case report
GEO Series GSE178261. Homo sapiens. 1 samples. Type: Genome variation profiling by genome tiling array; Genome variation profiling by SNP array.
H3K27-mutant diffuse hemispheric glioma presenting typical molecular features of diffuse midline glioma: A case report and literature review.
GEO Series GSE286743. Homo sapiens. 1 samples. Type: Methylation profiling by array.
Cancer incidence and treatment utilization patterns at a regional cancer center in Tanzania from 2008-2016: Initial report of 2,772 cases
This descriptive, retrospective study reviewed all cancer cases recorded in the Bugando Cancer Registry (BCR), a clinical and pathology based registry at the only cancer referral hospital in the region. Primary tumor site, method of diagnosis, HIV status, and cancer treatment were reported. Using census data, the 2012 GLOBOCAN estimates for Tanzania were scaled to the Lake Zone and adjusted for 2016 population growth. These estimates were then compared to BCR cases using one-sample tests of proportion. Here we report the pediatric cancer cases.
Dataset related to the article "Cryoablation of Atrial Fibrillation With the Fourth-Generation Balloon: The First Reported Case"
<p>This record contains raw data related to the article "Cryoablation of Atrial Fibrillation With the Fourth-Generation Balloon: The First Reported Case"</p> <p>ABSTRACT</p> <p>Cryoballoon ablation was developed as a new treatment for pulmonary vein (PV) isolation and has demonstrated high procedural success and comforting long-term clinical outcome. However, some improvements are necessary for real-time visualization of PV signals that appeared important to increase the efficacy and reduce ineffective cryoapplications. We report, for the first time, a cryoablation procedure using the fourth-generation cryoballoon, describing betterment in vein signal recording and acute procedural success.</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>
Occasionally Detection of Lupus Erythematosus cells in bone marrow sample: A case report
<p>SLE is a heterogeneous systemic autoimmune disease. Lupus Erythematosus cells (LE) are mature neutrophils, and phagocytized cells. In this case report, the observation of these cells in the bone marrow aspirate (BMA) raised the suspicion of SLE.</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>
Thyroid cancer harboring PTEN and TP53 mutations: A peculiar molecular and clinical case report
<p>To date, the molecular mechanisms that underline aggressiveness and resistance to tyrosine kinase inhibitors in some thyroid carcinomas (TCs) are not known yet. We report the case of a young patient with a metastatic poorly differentiated (PDTC) and follicular thyroid carcinoma (FTC) refractory to conventional therapies and to Sorafenib. The patient, despite an initial partial response, died of progressive disease 21 months after diagnosis. The genetic analysis performed on the primary tumor and on lymph nodes and distant metastases allowed to identify a frameshift mutation (p.P248Tfs*5) in the <em>PTEN</em> gene, never described in TC. This mutation was present in the primary tumor and, with a lower allelic frequency, in metastases diagnosed after treatment with Sorafenib. Mutations in <em>TP53</em> (p.C135Y and c.920-2A>G previously detected in anaplastic carcinomas and p.M133R never found in TC) were also detected in the primary tissue together with a mono-allelic expression of the p.C135Y mutant at RNA level. At metastatic sites level, we found only the <em>TP53</em> splicing mutation c.920-2A>G. The presence of defects in mismatch repair (MMR) proteins and genomic instability was also evaluated. The primary tumor showed a partial expression of MMR proteins together with a strong genomic instability. In conclusion, we demonstrated that the rare combination of somatic <em>PTEN</em> and <em>TP53</em> mutations in a patient with a metastatic FTC, together with the presence of tumor heterogeneity and genomic instability, might be associated with a high tumor aggressiveness and resistance to treatments.</p>
ScienceDex guides
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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.