History – 28 yrs age gravid female with history of past LSCS delivery. USG done about 1 month back suggesting relative low intrauterine pregnancy (images not available). Patient did not want to continue the pregnancy due to unknown reasons & hence MTP was attempted following which minimal PV bleed occurred without any definite expulsion of products. Patient was referred for MRI pelvis to assess the present status of the gestation sac & to look for the status of uterine scar from previous...
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Publication date: Available online 19 March 2020Source: Journal of Neuroscience MethodsAuthor(s): Catherine E. Davey, Artemio Soto-Breceda, Anthony Shafton, Robin M. McAllen, John B. Furness, David B. Grayden, Martin J. Stebbing
Thu Mar 19, 2020 14:42
Publication date: Available online 18 March 2020Source: Journal of Neuroscience MethodsAuthor(s): Yichao Ou, Mingfeng Zhou, Guangsen Wu, Haodong Gong, Kai Li, Xingqin Wang, Junjie Peng, Peirong Niu, Yawei Liu, Songtao Qi, Zhanpeng Feng
Thu Mar 19, 2020 14:42
Related Articles[Using the big data ofinternet to understand coronavirus disease 2019's symptom characteristics: a big data study]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2020 Mar 18;55(0):E004 Authors: Qiu HJ, Yuan LX, Huang XK, Zhou YQ, Wu QW, Zheng R, Yang QT Abstract Objective: Analyzing the symptom characteristics of Coronavirus Disease 2019(COVID-19) to improve its prevention. Methods: Using Baidu Index Platform (http://index.baidu.com)...
Thu Mar 19, 2020 14:42
Acute aortic dissection (AAD) is a catastrophic cardiovascular disease with high disability and mortality due to multiple fatal complications. However, the molecular changes of the serum proteome after AAD are not very clear. Here, we performed isobaric tags for relative and absolute quantitation- (iTRAQ-) based comparative proteomic analysis to investigate the proteome profile changes after AAD by collecting plasma samples from 20 AAD patients and 20 controls. Out of the 345 identified proteins,...
Thu Mar 19, 2020 13:20
Zusammenfassung Schwindelsyndrome haben oft keine oder nur unspezifische Biomarker. Deshalb erfordert ihre Definition eine Herangehensweise, die sich auf operationale Kriterien von Symptomkonstellationen stützt, d. h. dem Vorhandensein von Ein- und Ausschlusskriterien – ähnlich wie bei Kopfschmerzsyndromen und psychiatrischen Erkrankungen. Vor 10 Jahren begann die Bárány-Gesellschaft damit, eine Internationale Klassifikation Vestibulärer Krankheiten (ICVD, International Classification...
Thu Mar 19, 2020 02:00
Abstract RAD21 encodes a key component of the cohesin complex, and variants in RAD21 have been associated with Cornelia de Lange Syndrome (CdLS). Limited information on phenotypes attributable to RAD21 variants and genotype–phenotype relationships is currently published. We gathered a series of 49 individuals from 33 families with RAD21 alterations [24 different intragenic sequence variants (2 recurrent), 7 unique microdeletions], including 24 hitherto unpublished cases. We evaluated...
Thu Mar 19, 2020 02:00
Presentation of Case. Dr. Ryan J. Sullivan: A 64-year-old man presented to this hospital for evaluation of a mass in the left frontal and left parietal lobes. Four weeks before this presentation, while residing at his home in Florida, the patient began to have clumsiness of the right upper arm, as…
Thu Mar 19, 2020 02:00
Neurofibromatosis type 1, an autosomal dominant genetic disorder characterized by multiple progressive tumor and nontumor manifestations, has limited treatment options. In patients with the disorder, dysfunction of the guanosine triphosphatase–activating protein neurofibromin leads to…
Wed Mar 18, 2020 02:00
Hereditary angioedema is a rare, potentially life-threatening disorder characterized by attacks of cutaneous and submucosal swelling. Quincke first described its clinical presentation, and Osler’s recognition of the autosomal dominant inheritance pattern followed in 1888. The initial name of the…
Thu Mar 19, 2020 02:00
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