Results 51 to 60 of about 35,187 (207)
Journal of Intelligent Medicine, EarlyView.Abstract Acute kidney injury (AKI) is a common and severe complication of rhabdomyolysis (RM), and early risk stratification remains challenging because of its multifactorial and heterogeneous nature. We developed and externally validated an interpretable machine learning (ML) model for early prediction of AKI in RM across traumatic and non‐traumatic ...
Chunli Liu +11 more
wiley +1 more source
Molecular Genetics and Metabolism Reports, 2018 Introduction: Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is an autosomal recessive mitochondrial fatty acid oxidation disorder and presents as hypoketotic hypoglycemia or rhabdomyolysis during childhood.
Kenji Watanabe +3 more
doaj +1 more source
MEK Inhibitor Associated Airway Injury in an Infant With Noonan Syndrome: A Case Report
The Laryngoscope, EarlyView.An infant with Noonan syndrome treated with trametinib developed extensive mucosal sloughing of the upper and lower airway, followed by severe supraglottic scarring. Clinicians should consider airway toxicity as a potential adverse effect of MEK inhibitor therapy.
Veronica Drozdowski‐Nuccio +4 more
wiley +1 more source
Acute Kidney Injury Secondary to Hypothyroidism-Induced Rhabdomyolysis
Turkish Journal of Nephrology, 2019 Acute renal impairment due to rhabdomyolysis in patients with hypothyroidism is quite rare. We describe a case of acute kidney injury due to hypothyroidism-induced rhabdomyolysis in a 47-year-old man who was under levothyroxine medication.
Ramazan ULU +4 more
doaj
, 2017 Rhabdomyolysis is commonly defined as elevation of serum creatine kinase (sCK) level of above 10 times the upper limit of normal followed by a rapid decrease to normal values.
최영철, 이정환
core
Movement Disorders Clinical Practice, EarlyView.Abstract Background Childhood‐onset hyperkinetic movement disorders occur in a range of genetic conditions. Recently, there has been an increase in recognition of hyperkinetic movement disorders, mainly dystonia, chorea and dyskinesia, with monogenic conditions associated with neurodevelopmental delay (NDD) and also with developmental and epileptic ...
Hugo Morales‐Briceño +6 more
wiley +1 more source
, 2008 Virus-induced myopathy can be an important cause of life-threatening rhabdomyolysis. We report the case of a 30-year-old patient who developed rhabdomyolysis and acute renal failure in association with herpes simplex virus ...
Seetharaman, Mythili, MD +1 more
core +1 more source
A Gap Analysis of Deep Brain Stimulation for Childhood‐Onset Movement Disorders
Movement Disorders, EarlyView.Abstract Background Deep brain stimulation (DBS) is an established and increasingly utilized therapy for childhood‐onset movement disorders. However, pediatric DBS poses unique challenges that are not adequately addressed by adult‐derived paradigms. Objective To identify key gaps in the current use of DBS in childhood‐onset movement disorders and to ...
Daniela Munoz‐Chesta +6 more
wiley +1 more source
Therapeutic Effects of Procainamide on Endotoxin-Induced Rhabdomyolysis in Rats.
PLoS ONE, 2016 Overt systemic inflammatory response is a predisposing mechanism for infection-induced skeletal muscle damage and rhabdomyolysis. Aberrant DNA methylation plays a crucial role in the pathophysiology of excessive inflammatory response.
Chih-Chin Shih +6 more
doaj +1 more source
Journal of Medical Case Reports, 2018 Background Rhabdomyolysis is a rare but serious complication of lipid-lowering therapy. Statin and fibrate combination increases the risk of rhabdomyolysis possibly by pharmacodynamic interactions.
Chamara Dalugama +2 more
doaj +1 more source