Association of Fentanyl Overdose in Acute Amnestic Syndrome
In the present study, researchers examined the patients with the acute amnestic syndrome to determine the presence of Fentanyl traces in urine through Immunoassays
In the present study, researchers examined the patients with the acute amnestic syndrome to determine the presence of Fentanyl traces in urine through Immunoassays
In recent studies, scientists found genetic profiling could help determine whether an embryo created through in-vitro fertilization (IVF) is likely to successfully transfer to the womb, increasing the success rate of the procedure
In the study, researchers demonstrated that nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) conjugation to magnetic nanoparticles (MNP) increases their stability
The present study provides evidence that a long-term consumption of caffeine has negative effects on Alzheimer's disease, worsening the neuropsychiatric symptoms appearing in the majority of those affected by the disorder
According to new research in the American Heart Association's journal Circulation, women who give birth to infants with congenital heart defects may have an increased risk of cardiovascular hospitalizations later in life
According to research, the study was conducted to evaluate the effect of different bisphosphonates on the efficacy and safety of renal transplant patients through the online Metasystem.
The present study is conducted to determine the mechanism of renal protective effect of polysulfide to prevent nephrotoxicity caused by a chemotherapeutic drug cisplatin
A team led by scientists at Van Andel Research Institute (VARI) and Cedars-Sinai have developed a straightforward, computational way to measure cellular age, a feat that may lead to better, simpler screening and monitoring methods for cancer and other diseases.
A new study estimated that women with dark, coarse hair growth on the face, chest or back should be tested for polycystic ovary syndrome and other underlying health problems. The study was published in The Journal of Clinical Endocrinology & Metabolism.
According to the new research, rare genetic mutations associated with impairment of the breathing muscles are more common in children who have died from sudden infant death syndrome (SIDS) than in healthy controls
Atopic dermatitis is a chronic, recurrent inflammatory skin disease, which is frequently familial. The main cause of the disease seems to be a defect of the epidermal barrier resulting from a genetic predisposition concerning the epidermis, functioning of the immune system as well as environmental factors. Genes responsible for encoding protein S100, filaggrin, proteases and their inhibitors are the main genes related to the problem of epidermal barrier dysfunction.
According to a study, researchers declined most emergency department(ED), doctors underestimated the number of opioids prescriptions was began prescribing fewer upon learning of their behavior, according to results of a study published in Academic Emergency Medicine.