Results 141 to 150 of about 72,242 (280)
Pentalogy of Cantrell compiles the union of five anomalies including defects of the midline abdominal wall, lower sternum, anterior diaphragm, diaphragmatic pericardium, and any form of intra-cardiac pathology 1.
Vaibhav Maheshwari, Manoranjan Sahoo
doaj +1 more source
ABSTRACT Balloon‐assisted transseptal puncture across a large atrial septal defect closure device can permit pulsed‐field ablation in selected patients with complex septal anatomy, achieving durable pulmonary vein isolation and sinus rhythm. A borderline residual left‐to‐right shunt developed post‐procedure but decreased on serial imaging without ...
Ahmed Abdelrazik +5 more
wiley +1 more source
Background and aimsProgress in cardiology has extended the lifespan of patients with congenital heart defects (CHD). Cyanotic patients are exposed to typical diseases of adulthood, including atherosclerosis. Rheological changes typical of cyanosis affect
Sonia Alicja Nartowicz +7 more
doaj +1 more source
Penile Strangulation in a 68 Years Old Male by Plastic Bottleneck: A Case Report
ABSTRACT Penile strangulation is an uncommon urological emergency. The patient is a 68‐year‐old man with penile constriction caused by using plastic bottles resulting in distal edema. Liston bone cutter was used to remove the object under local anesthesia without open surgery. The urinary and erectile functions were maintained.
Nafisa Zaman Akhtar +6 more
wiley +1 more source
Eisenmenger syndrome: current perspectives
Heba Nashat,1–3 Aleksander Kempny,1–3 Colm McCabe,1 Laura C Price,1–3 Carl Harries,1 Rafael Alonso-Gonzalez,1–3 Michael A Gatzoulis,1–3 Stephen J Wort,1–3 Konstantinos Dimopoulos1–3 1Adult Congenital Heart Centre
Nashat H +8 more
doaj
ABSTRACT Patau syndrome (trisomy 13) is a life‐limiting chromosomal disorder with multiple congenital anomalies. We report a term male neonate with bilateral cleft lip and palate, aplasia cutis congenita, postaxial polydactyly, hypotonia, congenital heart disease, and presumed neonatal sepsis.
Sayed Hussain Amiri +4 more
wiley +1 more source
Early Acitretin Therapy in a Patient With Harlequin Ichthyosis
ABSTRACT Harlequin ichthyosis (HI) is a rare, severe congenital disorder of keratinization caused by pathogenic variants in the ABCA12 gene resulting in thick, hyperkeratotic plates, deep fissures, and characteristic facial and limb abnormalities.
Orasa Sukmark +2 more
wiley +1 more source
Transition Metal Chalcogenides: Perspectives on Their Applications for Nitrate Reduction
This review paper reports the syntheses, properties, and applications of TMCs for electrochemical reduction of nitrate to ammonia. Various studies revealed that the conversion of nitrate to ammonia is principally the electrocatalytic hydrogenation of nitrate and the rate and yield of ammonia is competitively challenged by hydrogen evolution reaction ...
Martins O. Omorogie
wiley +1 more source
Congenital methaemoglobinaemia: an infrequent cause of neonatal cyanosis
We present a case study of a newborn girl with a reduced erythrocytic nicotinamide adenine dinucleotide (NADH)-dependent methaemoglobin reductase level. Within the first days of life she developed cyanosis due to a methaemoglobin level of 21%.
Christensen, Ernst +3 more
core +1 more source
Traditional Chinese Medicine for lung cancer: Mechanisms, clinical evidence, and future perspectives
Graphical abstract represents the risk factors for lung cancer, TCM efficacy and clinical outcomes to future challenges. Abstract Lung cancer remains a leading cause of global cancer mortality. Despite advances in conventional treatments such as surgery, chemotherapy, targeted therapy, and immunotherapy, challenges including drug resistance, toxicity ...
Zhangdeng Chen, Liujun Bao
wiley +1 more source

