Results 91 to 100 of about 27,074 (259)

Forensic medical examination in the practice of an ophthalmologist

open access: yesModern technologies in ophtalmology, 2020
N.V. Fomina, E.I. Saidasheva
openaire   +1 more source

Integrative Genomic and Functional Investigation of the Multi‐Layered Genetic Architecture Between Anorexia Nervosa and Bone Loss

open access: yesInternational Journal of Eating Disorders, EarlyView.
ABSTRACT Objective Bone loss is a severe and often irreversible complication of anorexia nervosa (AN), yet the genetic mechanisms underlying this comorbidity remain underexplored. This study focuses on constructing a comprehensive genetic architecture between AN and estimated calcaneal bone mineral density (eBMD).
Tao Han   +14 more
wiley   +1 more source

Do witnesses of functional/dissociative seizures recall them accurately? A UK experimental study of semiology recall at clinically relevant time points with a pilot intervention

open access: yesEpilepsia, EarlyView.
Abstract Objective Different causes of transient loss of consciousness (TLOC) carry distinct risks and require different management. Early accurate diagnosis is essential to guide counseling, investigation, and referral. In routine practice, frontline clinicians and specialists often rely on eyewitness accounts, yet the reliability of witness testimony
Adam John Noble   +11 more
wiley   +1 more source

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort

open access: yesEpilepsia, EarlyView.
Abstract The association between autism spectrum disorder (hereafter referred to as autism) and tuberous sclerosis complex (TSC) is well established, yet the developmental pathways linking genetic mutation, cortical pathology, and epilepsy with autism remain unclear. The Tuberous Sclerosis 2000 Study recruited children newly diagnosed with TSC (N = 125)
Fiona S. McEwen   +12 more
wiley   +1 more source

MODERN SYNTHETIC OPIOIDS AND RABDOMYOLISIS: CLINICAL AND FORENSIC ASPECTS

open access: yesКлінічна та профілактична медицина
Introduction. Every year, the list of chemical substances, including drugs, that can potentially cause rhabdomyolysis grows worldwide. Aim. Analysis of etiological factors that caused the development of rhabdomyolysis of non-traumatic genesis in adult
Natalia V. Kurdil   +6 more
doaj   +1 more source

ER‐Localized Deadenylase PNLDC1 Suppresses Colorectal Cancer Progression by Targeting the mRNA Decay of TUBB4B

open access: yesExploration, EarlyView.
The deficiency of PNLDC1 exacerbates the advancement of CRC. PNLDC1 interacts with TUBB4B mRNA to regulate the p53–p21–CDK2–cyclin E2 pathway, thereby influencing the G2/M phase of the cell cycle. ABSTRACT Colorectal cancer (CRC) remains a leading cause of cancer‐related mortality, highlighting the urgent need for novel therapeutic strategies.
Lexin Liu   +18 more
wiley   +1 more source

[Histopathological examinations in forensic medical expertise].

open access: yesArchiwum medycyny sadowej i kryminologii, 2007
The report reviews the role of histopathology in legal proceedings. The author emphasizes the probative value of results of histopathological analyses, carried out supplementary to post-mortem macroscopic examinations. The issue of recommendations for such examinations is addressed, and the possibilities of employing histopathology for purposes other ...
openaire   +1 more source

Effect of Ammonium Polyphosphate/Silicate Content on the Postfire Mechanics of Epoxy Glass‐Fiber Composites Using Facile Chocolate Bar‐Inspired Structures

open access: yesFire and Materials, Volume 49, Issue 3, Page 329-346, April 2025.
ABSTRACT This study investigates the postfire mechanical properties of epoxy glass‐fiber reinforced composites (EP GFRCs) using increasing concentrations of ammonium polyphosphate (APP) and inorganic silicate (InSi) to modify the char and fire residue.
Sruthi Sunder   +5 more
wiley   +1 more source

Fahr’s disease (clinical case)

open access: yesИзвестия высших учебных заведений. Поволжский регион: Медицинские науки
This article reviews a clinical case of Fahr’s disease. This pathology is a rare hereditary or sporadic neurological disease characterised by abnormal calcium deposition in the basal ganglia and dentate nuclei of the cerebellum.
Marija G. Fedorova   +4 more
doaj   +1 more source

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