Results 1 to 10 of about 12,404,465 (380)

Case for diagnosis [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2014
Intravascular papillary endothelial hyperplasia is a benign vascular lesion caused by proliferation of endothelium. It is reactive to thrombotic or inflammatory stimuli in the vessel wall.We report the case of a 14-yearold male patient with a violet-colored erythematous tumoral lesion of progressive growth in the occipital region.
Fabre, Andréa Buosi   +5 more
  +30 more sources

Polymorphisms in Genes of Lipid Metabolism Are Associated with Type 2 Diabetes Mellitus and Periodontitis, as Comorbidities, and with the Subjects’ Periodontal, Glycemic, and Lipid Profiles

open access: yesJournal of Diabetes Research, 2021
Background. Type 2 diabetes mellitus (T2DM) and periodontitis (P) commonly occur as comorbidities, but the commonalities in the genetic makeup of affected individuals is largely unknown. Since dyslipidemia is a frequent condition in these individuals, we
Ingra G. Nicchio   +9 more
doaj   +1 more source

Myeloid-Derived Suppressor Cells and CD68+CD163+M2-Like Macrophages as Therapeutic Response Biomarkers Are Associated with Plasma Inflammatory Cytokines: A Preliminary Study for Non-Small Cell Lung Cancer Patients in Radiotherapy

open access: yesJournal of Immunology Research, 2022
Background. Recent studies show that myeloid-derived suppressor cells (MDSCs) and M2-like macrophages are involved in the treatment of tumors; however, their therapeutic response role is rarely known in non-small cell lung cancer (NSCLC) during ...
Minghe Lv   +7 more
doaj   +1 more source

2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure

open access: yesEuropean Journal of Heart Failure, 2022
Document Reviewers: Rudolf A. de Boer (CPG Review Coordinator) (Netherlands), P. Christian Schulze (CPG Review Coordinator) (Germany), Magdy Abdelhamid (Egypt), Victor Aboyans (France), Stamatis Adamopoulos (Greece), Stefan D.
T. McDonagh   +30 more
semanticscholar   +1 more source

Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies

open access: yesGenetics Research, 2022
Objective. The current study aimed to compare the characteristics of chromosome abnormalities detected by conventional G-banding karyotyping, chromosome microarray analysis (CMA), or fluorescence in situ hybridization (FISH)/CNVplex analysis and further ...
Jin Wang   +9 more
doaj   +1 more source

Round ligament varices mimicking inguinal hernia during pregnancy

open access: yesRadiology Case Reports, 2019
Varicosities of the round ligament is a rare condition. Our gravid patient had left inguinal swelling noticeable for 2 weeks and pain on and off. Swelling was reducible and treating surgeon referred patient for ultrasound to rule out inguinal hernia ...
Shailendra Singh Naik, MD, DNB Radio diagnosis, MNAMS   +1 more
doaj   +1 more source

Mining Potential Drug Targets and Constructing Diagnostic Models for Heart Failure Based on miRNA-mRNA Networks

open access: yesMediators of Inflammation, 2022
Heart failure (HF) is a globally prevalent cardiovascular disease, but effective drug targets and diagnostic models are still lacking. This study was designed to investigate effective drug targets and diagnostic models for HF in terms of miRNA targets ...
Xiangming Fang   +4 more
doaj   +1 more source

Sarcopenia: revised European consensus on definition and diagnosis

open access: yesAge and Ageing, 2018
Background in 2010, the European Working Group on Sarcopenia in Older People (EWGSOP) published a sarcopenia definition that aimed to foster advances in identifying and caring for people with sarcopenia.
A. Cruz-Jentoft   +28 more
semanticscholar   +1 more source

Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array

open access: yesMolecular Cytogenetics, 2023
Background With the application of chromosome microarray, next-generation sequencing and other highly sensitive genetic techniques in disease diagnosis, the detection of mosaicism has become increasingly prevalent.
Lili Zhou   +5 more
doaj   +1 more source

Prenatal diagnosis of 7 cases with uniparental disomy by utilization of single nucleotide polymorphism array

open access: yesMolecular Cytogenetics, 2021
Background The phenotypes of uniparental disomy (UPD) are variable, which may either have no clinical impact, lead to clinical signs and symptoms. Molecular analysis is essential for making a correct diagnosis.
Lili Zhou   +5 more
doaj   +1 more source

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