Results 11 to 20 of about 130,707 (355)
Incorporating a Spatial Prior into Nonlinear D-Bar EIT imaging for Complex Admittivities [PDF]
arXiv, 2016 Electrical Impedance Tomography (EIT) aims to recover the internal conductivity and permittivity distributions of a body from electrical measurements taken on electrodes on the surface of the body. The reconstruction task is a severely ill-posed nonlinear inverse problem that is highly sensitive to measurement noise and modeling errors.
Alsaker, Melody +2 more
arxiv +5 more sources
Annals of Gastroenterological Surgery, Volume 7, Issue 1, Page 131-137, January 2023., 2023 The cornerstone of treatment for symptomatic gallbladder stones is laparoscopic cholecystectomy. Pain is the commonest cause of extended hospital stay. Disturbance of liver—diaphragm surface tension is the main cause of pain. Retained CO2 is a major concern post laparoscopic cholecystectomy.
Mohamed Lotfy Ali Abuelzein +3 more
wiley +1 more source
Folliculin haploinsufficiency causes cellular dysfunction of pleural mesothelial cells
Scientific Reports, 2021 Birt–Hogg–Dubé syndrome (BHDS), an autosomal dominant inheritance disease caused by folliculin (FLCN) mutations, is associated with lung cysts and spontaneous pneumothorax.
Shouichi Okamoto +11 more
doaj +1 more source
American Journal of Medical Genetics Part A, Volume 191, Issue 1, Page 37-51, January 2023., 2023 Abstract Vascular Ehlers–Danlos syndrome (vEDS) is a hereditary connective tissue disorder (HCTD) characterized by arterial dissection/aneurysm/rupture, sigmoid colon rupture, or uterine rupture. Diagnosis is confirmed by detecting heterozygous variants in COL3A1.
Tomomi Yamaguchi +25 more
wiley +1 more source
American Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 332-337, February 2023., 2023 Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings +1 more
wiley +1 more source
BMC Pulmonary Medicine, 2022 Background Pneumocystis jirovecii pneumonia (PCP) with acute respiratory failure can result in development of pneumothorax during treatment. This study aimed to identify the incidence and related factors of pneumothorax in patients with PCP and acute ...
Ji Soo Choi +17 more
doaj +1 more source
Cancer, Volume 129, Issue 2, Page 283-295, 15 January 2023., 2023 Abstract Background Antibody–drug conjugates (ADCs) have complex molecular structures and have been tested in numerous clinical trials. Therefore, understanding the mechanisms of their toxicity when applied in medical practice is of high importance. Methods In a systematic review and meta‐analysis of data gathered from different scientific databases ...
Youwen Zhu +3 more
wiley +1 more source
The Clinical Respiratory Journal, 2022 Objectives Delayed pneumothorax can cause an emergency room visit and be life‐threatening in case of tension pneumothorax after transthoracic needle biopsy.
Jeong Suk Koh +8 more
doaj +1 more source
Electrocardiographic alterations by pneumothorax: a case-control study with review of the literature
Swiss Medical Weekly, 2021 BACKGROUND: Numerous ECG alterations due to pneumothorax have been reported. The objective of the study was to establish the presence of ECG changes associated with pneumothorax in the literature, and in a cohort of patients with proven pneumothorax ...
Bruno Minotti +5 more
doaj +1 more source
BMC Pulmonary Medicine, 2021 Background We aim to analyze the risk factors for pneumothorax associated with computed tomography (CT)-guided percutaneous core needle biopsy (PCNB) of the lung. Whether the lung function characteristics are related to pneumothorax is unclear.
Chunhai Li +7 more
doaj +1 more source