Results 141 to 150 of about 912,627 (390)

An Ethics Framework for Medical Assistance in Dying: Supporting Ethical Decision‐Making in the Practice of MAiD

open access: yesBioethics, EarlyView.
ABSTRACT This paper presents an Ethics Framework for MAiD (Medical Assistance in Dying) to support the integration of evidence‐informed, values‐based, inclusive and transparent ethical decision‐making into everyday MAiD practice. As with other areas of clinical practice, ethical decision‐making is an intrinsic part of MAiD.
Andrea N. Frolic, Tim Holland
wiley   +1 more source

Whole genome sequencing for mutation discovery in a single case of lysosomal storage disease (MPS type 1) in the dog. [PDF]

open access: yes, 2020
Mucopolysaccharidosis (MPS) is a metabolic storage disorder caused by the deficiency of any lysosomal enzyme required for the breakdown of glycosaminoglycans.
Aguilar, Miriam   +13 more
core   +3 more sources

Robotic surgery for paediatric neurogenic lower urinary tract dysfunction: a systematic review

open access: yesBJU International, Volume 135, Issue 4, Page 557-566, April 2025.
Objective To evaluate in a systematic review the outcomes, benefits, and limitations of robot‐assisted surgeries for paediatric neurogenic lower urinary tract dysfunction (LUTD), as robot‐assisted techniques have emerged as a potential alternative, offering enhanced precision, dexterity, and visualisation.
Ihtisham Ahmad   +6 more
wiley   +1 more source

Cardiovascular Health in Women—Across the Lifespan

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar   +5 more
wiley   +1 more source

Expanding the Genotype and Phenotype Diversity in a Chinese Cohort With TRPV4‐Related Dysplasia

open access: yesClinical Genetics, EarlyView.
Exploring the genotype and phenotype diversity in a Chinese cohort with TRPV4‐related dysplasia. ABSTRACT Dominant mutations in the calcium permeable ion channel TRPV4 (transient receptor potential vanilloid 4) typically result in skeletal dysplasia or peripheral neuromuscular disease.
Lina Dong   +8 more
wiley   +1 more source

Diffusion Tensor Imaging in a Large Longitudinal Series of Patients With Cervical Spondylotic Myelopathy Correlated With Long-Term Functional Outcome [PDF]

open access: yes, 2018
BACKGROUND Fractional anisotropy (FA) of the high cervical cord correlates with upper limb function in acute cervical cord injury. We investigated the correlation between preoperative FA at the level of maximal compression and functional recovery in a ...
Budde, Matthew D.   +8 more
core   +1 more source

Prevalence and Associated Factors of Olfactory and Gustatory Loss in Patients With Nasal Septal Deviation

open access: yesClinical Otolaryngology, EarlyView.
ABSTRACT Objectives This study aimed to evaluate the olfactory and gustatory functions of patients with nasal septal deviation (NSD) and identify the factors associated with olfactory loss (OL) and gustatory loss (GL). Design and Setting Retrospective data analysis of cohort group. Participants Two‐hundred fourteen adult patients with NSD at a tertiary
Ja‐Yoon Kim   +3 more
wiley   +1 more source

Development of Lumbar Spinal Stenosis Caused by Lumbar Vertebral Compression Fracture

open access: yesTürk Osteoporoz Dergisi, 2004
Spinal stenosis is a narrowing of the spinal canal by a combination of bone and soft tissues, which causes mechanical compression of spinal nerve roots.Diagnosis is made by computerized tomography, myelography, or magnetic resonance (MR) imaging. The aim
Hidayet Sarı   +2 more
doaj  

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