Metastases of Hepatocellular Carcinoma Misdiagnosed as Isolated Hypertrophic Cardiomyopathy.
In conclusion, we suggest that the ultrasound appearance of hypertrophic cardiomyopathy in hepatocellular carcinoma patients should be seen as a "red flag" and recommend the introduction of magnetic resonance imaging assessment of transplant candidates. PMID: 31171339 [PubMed]
Conclusions: The transduodenal approach for obtaining samples from solid lesions using a 19-G flexible needle seems feasible and accurate. PMID: 32447874 [PubMed - as supplied by publisher]
It’s been enough for a bit, isn’t it? For three months now, there has been little space in the world for any other kind of news. That is, news without the word ‘coronavirus’. But there was innovation, there is excitement and, well, even some weird (although useful!) inventions that appeared while the world has been in lockdown. So here’s an outlook on such news, all, promise, without that particular C-word. Hospitals have been facing great challenges recently. But they are on the verge of a new era that brings better care and more focus on the patient. This is a trend we have been talking a...
Publication date: Available online 24 May 2020Source: Materials Science and Engineering: AAuthor(s): Y.C. Wang, L.M. Lei, L. Shi, H.Y. Wan, F. Liang, G.P. Zhang
Publication date: Available online 24 May 2020Source: Chemical Engineering and Processing - Process IntensificationAuthor(s): Sajad Shokri, Seyed Shahram Shekarforoush, Saeid Hosseinzadeh
Publication date: Available online 24 May 2020Source: Chemical Engineering and Processing - Process IntensificationAuthor(s): R.M. González-Balderas, S.B. Velásquez-Orta, M.T. Orta Ledesma
ConclusionPurr is a low-level Rust library for working with SMILES. It currently includes a parser that, while not complete, would not take much effort or knowledge of Rust to finish. A SMILES writer should be straightforward to implement given a depth-first traversal and existing Purr data structures. The combination of a low-levelMolecule implementation as already described, and a Purr reader/writer would create a solid foundation for a future cheminformatics toolkit in Rust.
Authors: Aktuglu-Zeybek AC, Kiykim E, Cansever MS Abstract Hereditary tyrosinemia type 1 (HT1, OMIM 276700) is a rare autosomal recessively inherited inborn error of metabolism in the tyrosine catabolic pathway due to deficiency of the enzyme fumarylacetoacetate hydrolase. The clinical features of HT1 are widely heterogenous even within the same family members. Clinical features includes acute or chronic liver disease with increased risk of hepatocellular carcinoma, hypophosphatemic rickets due to renal tubular dysfunction, glomerulosclerosis, failure to thrive, neurological porphyria-like crisis, hypertrophic card...