Results 1 to 10 of about 12,742,253 (357)
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
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
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
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
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
Diagnosis in vascular dementia, applying ‘Cochrane diagnosis rules’ to ‘dementia diagnostic tools’ [PDF]
In this issue of Clinical Science, Biesbroek and colleagues describe recent work on magnetic resonance imaging (MRI)-based cerebral lesion location and its association with cognitive decline.
McCleery, Jenny, Quinn, Terence J.
core +1 more source
Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations
Background The potential correlations between chromosomal abnormalities and craniofacial malformations (CFMs) remain a challenge in prenatal diagnosis.
Chenyang Xu +6 more
doaj +1 more source
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
Diagnosis of South Asia Specific Diseases [PDF]
Asian StudiesHindi Urdu FlagshipSouth Asia ...
Joshi, Himanshu +3 more
core +1 more source
Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array
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

