Results 51 to 60 of about 49,091 (283)

Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective We describe a series of pregnancies with autosomal dominant lymphedema and generalized lymphatic dysplasia in the fetus diagnosed with prenatal exome or genome sequencing. We focus on specific syndromes, fetal features, and parental symptoms to deepen our understanding of congenital lymphatic anomalies.
Sara G. Vargo   +4 more
wiley   +1 more source

Primary care physicians' perceptions of barriers and facilitators to management of chronic kidney disease: A mixed methods study. [PDF]

open access: yes, 2019
BackgroundGiven the high prevalence of chronic kidney disease (CKD), primary care physicians (PCPs) frequently manage early stage CKD. Nonetheless, there are challenges in providing optimal CKD care in the primary care setting.
Abdel-Kader, Khaled   +15 more
core   +1 more source

Multiscale Engineering of Ion‐Conducting Gels for Sustainable Bioelectronic Systems

open access: yesSmall Methods, EarlyView.
This review highlights multiscale engineering strategies for ion‐conducting gels aimed at achieving sustainable bioelectronic systems. It systematically examines material‐level, device‐level, and system‐level approaches to ensure long‐term stability and functional integrity under physiological conditions, integrating molecular design, device ...
Ji Hong Kim   +6 more
wiley   +1 more source

Use of Antihypertensive Agents and Association With Risk of Adverse Outcomes in Chronic Kidney Disease: Focus on Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers. [PDF]

open access: yes, 2018
Background Our objective was to determine patterns of antihypertensive agent use by stage of chronic kidney disease (CKD) and to evaluate the association between different classes of antihypertensive agents with nonrenal outcomes, especially in advanced ...
Johansen, Kirsten L   +4 more
core  

Incidence of Co-Trimoxazole-Induced Hyperkalemia in a Tertiary Care Hospital

open access: yesRisk Management and Healthcare Policy, 2021
Rana M Al AdAwi1 1, Zainab Albu-Mahmood1 1, Mohamed Abdelgelil1 1, Hani Abdelaziz,2 Derek Stewart3 3, Ahmed Awaisu3 1Clinical Pharmacist, Hamad General Hospital, Hamad Medical Corporation, Doha, Qatar; 2Clinical Pharmacist Supervisor, Al Wakra Hospital ...
Al AdAwi RM   +5 more
doaj  

Initial and Recurrent Hyperkalemia Events in Patients With CKD in Older Adults: A Population-Based Cohort Study

open access: yesCanadian Journal of Kidney Health and Disease, 2021
Background: The risk of hyperkalemia is elevated in chronic kidney disease (CKD); however, the initial and recurrent risk among older individuals is less clear.
Sriram Sriperumbuduri   +10 more
doaj   +1 more source

Explosive Weapons Trauma Care Collective (EXTRACCT) Clinical Practice Guideline: Resuscitation of Pediatric Blast Injury Patient

open access: yesWorld Journal of Surgery, EarlyView.
Children living in conflict or post‐conflict zones are frequently exposed to explosive injuries, with thousands killed and injured every year. The clinical practice guideline from the Explosive Weapons Trauma Care Collective (EXTRACCT) group provides a review of current best practice for the resuscitation of a child who has sustained a blast injury in ...
Gavin Wooldridge   +6 more
wiley   +1 more source

Integrating Dialysis in Ex Situ Machine Perfusion: A Systematic Review and Meta‐Analysis of Outcomes

open access: yesArtificial Organs, EarlyView.
Dialysis‐enhanced EVMP effectively maintains biochemical homeostasis, potentially mitigating metabolic stress and extending perfusion duration. Functional outcomes varied depending on the organ type, with the most pronounced benefits observed in cardiac perfusion.
Yomna E. Dean   +12 more
wiley   +1 more source

Oral transmucosal fentanyl [PDF]

open access: yes, 1998
None ...
D. Prosser   +4 more
core   +1 more source

Case Report: Compound Heterozygous SCNN1B Mutations Causing Pseudohypoaldosteronism Type 1B2 in Neonatal Twins. [PDF]

open access: yesMol Genet Genomic Med
First Chinese neonatal cases of systemic PHA1B from novel compound‐heterozygous SCNN1B variants (c.585+2T>C; c.1544T>C) presented with life‐threatening hyperkalemia and hyponatremia unresponsive to steroids. Early genetic testing enabled targeted sodium supplementation and potassium‐binding therapy, normalizing electrolytes and underscoring SCNN1B ...
Wang Z, Long L, Bi H.
europepmc   +2 more sources

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