Results 11 to 20 of about 8,808,626 (352)

Case for diagnosis [PDF]

Anais Brasileiros de Dermatologia, 2014
Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unknown etiology characterized by infarcts in the dermis, gastrointestinal tract, central nervous system, and other organs. It is characterized by papules, which become umbilicated and evolve with a depressed porcelain-white central area, with an erythematous
Lima, Lourenço de Azevedo, Haddad, Natacha de Carvalho Mello, Lima, Ricardo Barbosa, D'Acri, Antonio Macedo, Martins, Carlos José   +4 more
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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

Journal 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, Thamiris Cirelli, Rafael Nepomuceno, Marco A. R. Hidalgo, Carlos Rossa, Joni A. Cirelli, Silvana R. P. Orrico, Silvana P. Barros, Letícia H. Theodoro, Raquel M. Scarel-Caminaga   +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

Journal 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, Xibing Zhuang, Shali Shao, Xuan Li, Yunfeng Cheng, Duojiao Wu, Xiangdong Wang, Tiankui Qiao   +7 more
doaj   +1 more source

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

Genetics 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, Danni Wang, Yan Yin, Yi Deng, Mengling Ye, Ping Wei, Zhuo Zhang, Chun Chen, Shengfang Qin, Xueyan Wang   +9 more
doaj   +1 more source

Round ligament varices mimicking inguinal hernia during pregnancy

Radiology 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, Padhmini Balasubramanian, MD, DNB Radio diagnosis   +1 more
doaj   +1 more source

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

Mediators 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, Rensheng Song, Jiaxing Wei, Qin Liao, Zhenhong Zeng   +4 more
doaj   +1 more source

Post-Mortem diagnosis of dementia by informant interview. [PDF]

, 2010
The diagnosis of normal cognition or dementia in the Brazilian Brain Bank of the Aging Brain Study Group (BBBABSG) has relied on postmortem interview with an informant. Objectives:To ascertain the sensitivity and specificity of postmortem diagnosis based
Balbino, Érika Silvério, Battela, Camila, Brucki, Sonia Maria Dozzi, Campora, Flávia, Damin, Antonio Eduardo, Farfel, José Marcelo, Ferretti, Renata Eloah de Lucena, Grinberg, Lea Tenenholz, Jacob-Filho, Wilson, Leite, Renata Elaine Paraiso, Lima, Maria do Carmo de Ascenção, Moreira, Eliza Guccione, Morillo, Lilian Schafirovits, Nitrini, Ricardo, Pasqualucci, Carlos Augusto, Perroco, Tibor Rilho, Rosemberg, Sérgio, Ruiz, Lumena, Saldiva, Paulo Hilário Nascimento, Suemoto, Claudia Kimie   +19 more
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Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations

Molecular Cytogenetics, 2020
Background The potential correlations between chromosomal abnormalities and craniofacial malformations (CFMs) remain a challenge in prenatal diagnosis.
Chenyang Xu, Yanbao Xiang, Xueqin Xu, Lili Zhou, Huanzheng Li, Xueqin Dong, Shaohua Tang   +6 more
doaj   +1 more source

Diagnosis of South Asia Specific Diseases [PDF]

, 2010
Asian StudiesHindi Urdu FlagshipSouth Asia ...
Joshi, Himanshu, Nik Ilieva, Gabriela, Ranjan, Rakesh, Shankar, Jishnu   +3 more
core   +1 more source

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

Molecular 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, Zhaoke Zheng, Yunzhi Xu, Xiaoxiao Lv, Chenyang Xu, Xueqin Xu   +5 more
doaj   +1 more source