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| | {{ft|I}} | | {{ft|I}} |
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| | + | '''[[SARS-2 compared to anything]]''' |
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| | '''[[Parvovirus B19]]''' broad manif overlap, up to 75% igg prevalence, proportional to age, maybe a helper virus (my pretty idea 08/22th 2020) | | '''[[Parvovirus B19]]''' broad manif overlap, up to 75% igg prevalence, proportional to age, maybe a helper virus (my pretty idea 08/22th 2020) |
| | | | |
| − | personal opinion:
| + | '''[[SDP MERS]] ''' |
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| − | part of the '''microangiopathic-hemolytic anemia / HELLP / SIH / HUS / TTP spectrum''' bc:
| + | '''[[SDP SARS ]]''' |
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| − | 1. micro/thromboembolism
| + | '''[[SDP other human coronaviruses]] |
| − | 2. net's
| + | |
| − | 3. thrombocytopenia
| + | |
| − | 4. various neurological
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| − | 5. liver enzymes
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| − | data on vWF, adamts13, sflt3, vegf needed.
| + | '''[[SDP any pig swine coronaviruses]] |
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| − | '''Infectious vasculitis''' | + | '''[[SDP any cattle coronaviruses]] |
| − | *''Kawasaki might be infectious or something transmitted by intercontinental aerosols...''
| + | |
| − | *''Wegners responds to cotrim...''
| + | |
| − | *''NETosis is a pretty concept anything which triggers PMN...''
| + | |
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| − | '''MERS ''' | + | '''[[SDP any feline coronaviruses]] |
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| − | '''SARS ''' | + | '''[[SDP any murine coronaviruses]] |
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| − | '''Influenza ''' | + | '''[[SDP any avian coronaviruses]] |
| − | {{tp|p=32405236|t=2020. Comparative review of respiratory diseases caused by coronaviruses and influenza A viruses during epidemic season.|pdf=|usr=009}}
| + | |
| − | *[https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0028-1108874?fbclid=IwAR2j0XWPCVT8d4-JJHkKSLwUpSQP_PnvQo2idF6DtRW50kkAUdy_DqayOhI 1970 Influenza associated Pulmonary embolism]
| + | |
| | | | |
| | + | '''[[SDP any new animal coronaviruses]] |
| | | | |
| − | '''Influenza 1918 ''' | + | '''[[SDP any other animal coronaviruses]] |
| − | *[https://www.history.com/news/spanish-flu-second-wave-resurgence history.com]
| + | |
| | | | |
| − | '''anything Ebola '''
| |
| − | look as this (title only currently available to me) and the following on topic
| |
| − | {{tp|p=13833162|t=1959. Glomerular capillary endotheliosis in toxemia of pregnancy |pdf=|usr=}}
| |
| − | {{tp|p=14511965|t=2003. Glomerular endotheliosis in normal pregnancy and pre-eclampsia |pdf=|usr=}}
| |
| − | ----
| |
| | | | |
| | | | |
| | + | '''[[SDP Influenza]] ''' |
| | | | |
| | + | '''[[SDP Influenza 1918]] ''' |
| | | | |
| − | {{tp|p=31256729|t=2020. Narrative review of Middle East respiratory syndrome coronavirus (MERS-CoV) infection: updates and implications for practice.|pdf=|usr=018}}
| + | '''[[SDP Dengue]]''' |
| | | | |
| | + | '''[[SDP Ebola]] ''' |
| | | | |
| − | {{tp|p=32871999|t=2020. Human coronavirus OC43 infection associated pneumonia in a girl with acute lymphoblastic leukemia: A case report.|pdf=|usr=018}}
| + | ---- |
| − | {{tp|p=32785421|t=2020. A novel Betacoronavirus characterised in collared peccaries from the Rio de Janeiro Zoo (Brazil) killed by unknown disease.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31792450|t=2019. Structures of MERS-CoV spike glycoprotein in complex with sialoside attachment receptors.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32798533|t=2020. Medical features of COVID-19 and influenza infection: A comparative study in Paris, France.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32213247|t=2020. N-glycosylation of infectious bronchitis virus M41 spike determines receptor specificity.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31592752|t=2019. Isolation and growth characterization of novel full length and deletion mutant human MERS-CoV strains from clinical specimens collected during 2015.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31727466|t=2020. Focus on Middle East respiratory syndrome coronavirus (MERS-CoV).|pdf=|usr=018}}
| + | |
| − | | + | |
| − | {{tp|p=30064709|t=2020. Herd level estimation of probability of disease freedom applied on the Norwegian control program for bovine respiratory syncytial virus and bovine coronavirus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31900356|t=2020. Cryo-EM analysis of a feline coronavirus spike protein reveals a unique structure and camouflaging glycans.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32867979|t=2020. Alteration of immunological parameters in infectious bronchitis vaccinated-specific pathogen-free broilers after the use of different infectious bursal disease vaccines.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32416792|t=2020. Pathogenicity of a QX-like avian infectious bronchitis virus isolated in China.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32036979|t=2020. Research Note: First evidence of infectious bronchitis virus Middle-East GI-23 lineage (Var2-like) in Germany.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32343704|t=2020. Immune responses to porcine epidemic diarrhea virus (PEDV) in swine and protection against subsequent infection.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32730327|t=2020. Transferrin receptor 1 levels at the cell surface influence the susceptibility of newborn piglets to PEDV infection.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32059047|t=2020. A realistic two-strain model for MERS-CoV infection uncovers the high risk for epidemic propagation.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32610501|t=2020. The Effect of Natural Feline Coronavirus Infection on the Host Immune Response: A Whole-Transcriptome Analysis of the Mesenteric Lymph Nodes in Cats with and without Feline Infectious Peritonitis.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32635137|t=2020. Evaluation of Interferon-Gamma Polymorphisms as a Risk Factor in Feline Infectious Peritonitis Development in Non-Pedigree Cats-A Large Cohort Study.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32707796|t=2020. Correlation of Feline Coronavirus Shedding in Feces with Coronavirus Antibody Titer.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31963705|t=2020. In Vivo Antiviral Effects of U18666A Against Type I Feline Infectious Peritonitis Virus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32825430|t=2020. Buffalopox Virus: An Emerging Virus in Livestock and Humans.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32879801|t=2020. A comparison of COVID-19, SARS and MERS.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31835559|t=2019. Feline Infectious Peritonitis as a Systemic Inflammatory Disease: Contribution of Liver and Heart to the Pathogenesis.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32768236|t=2020. Cellular poly(C) binding protein 2 interacts with porcine epidemic diarrhea virus papain-like protease 1 and supports viral replication.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32041637|t=2020. PEDV enters cells through clathrin-, caveolae-, and lipid raft-mediated endocytosis and traffics via the endo-/lysosome pathway.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31706335|t=2019. Evolution of infectious bronchitis virus in the field after homologous vaccination introduction.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32580381|t=2020. Infectious Bronchitis Virus Evolution, Diagnosis and Control.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32493436|t=2020. Three kinds of treatment with Homoharringtonine, Hydroxychloroquine or shRNA and their combination against coronavirus PEDV in vitro.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32552831|t=2020. Challenge infection model for MERS-CoV based on naturally infected camels.|pdf=|usr=018}}
| + | |
| − | {{ttp|p=32094077|t=2020. Inhibitory effects of glycopyrronium, formoterol, and budesonide on coronavirus HCoV-229E replication and cytokine production by primary cultures of human nasal and tracheal epithelial cells.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32803835|t=2020. Comparative analysis of the genome structure and organization of the Middle East respiratory syndrome coronavirus (MERS-CoV) 2012 to 2019 revealing evidence for virus strain barcoding, zoonotic transmission, and selection pressure.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32792041|t=2020. Hydroxychloroquine and Coronavirus Disease 2019: A Systematic Review of a Scientific Failure.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32220667|t=2020. Oral Mutian(R)X stopped faecal feline coronavirus shedding by naturally infected cats.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31265112|t=2019. Simultaneous and visual detection of infectious bronchitis virus and Newcastle disease virus by multiple LAMP and lateral flow dipstick.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31264704|t=2019. Molecular epidemiology of infectious bronchitis virus and avian metapneumovirus in Greece.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31222258|t=2019. Molecular characteristics and pathogenicity analysis of QX-like avian infectious bronchitis virus isolated in China in 2017 and 2018.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31399745|t=2019. Vaccine or field strains: the jigsaw pattern of infectious bronchitis virus molecular epidemiology in Poland.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31399732|t=2019. Protective effects of hypericin against infectious bronchitis virus induced apoptosis and reactive oxygen species in chicken embryo kidney cells.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32245150|t=2020. Characterization of the Humoral Immune Response to Porcine Epidemic Diarrhea Virus Infection under Experimental and Field Conditions Using an AlphaLISA Platform.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32782912|t=2020. Prolonged (6-Month) Shedding of Middle East Respiratory Syndrome Coronavirus RNA in the Sputum of a Lymphoma Patient.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31924756|t=2020. Comparative therapeutic efficacy of remdesivir and combination lopinavir, ritonavir, and interferon beta against MERS-CoV.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31852899|t=2019. SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32065987|t=2020. Effect of TLR agonist on infections bronchitis virus replication and cytokine expression in embryonated chicken eggs.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31536759|t=2019. Comprehensive codon usage analysis of porcine deltacoronavirus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31505263|t=2019. Influenza A virus infection induces liver injury in mice.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32107296|t=2020. Complete Genome Sequence of Avian Coronavirus Strain GA08 (GI-27 Lineage).|pdf=|usr=018}}
| + | |
| − | {{tp|p=32107295|t=2020. A 25-Year-Old Sample Contributes the Complete Genome Sequence of Avian Coronavirus Vaccine Strain ArkDPI, Reisolated from Commercial Broilers in the United States.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32079638|t=2020. Complete Genome Sequences of Five Human Coronavirus NL63 Strains Causing Respiratory Illness in Hospitalized Children in China.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31727697|t=2019. Genome Sequences of Human Coronavirus OC43 and NL63, Associated with Respiratory Infections in Kilifi, Kenya.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32239666|t=2020. Porcine deltacoronavirus infection alters bacterial communities in the colon and feces of neonatal piglets.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32872640|t=2020. Dissecting Transcription Factor-Target Interaction in Bovine Coronavirus Infection.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32848272|t=2020. Increased Incidence, Morbidity, and Mortality in Human Coronavirus NL63 Associated with ACE Inhibitor Therapy and Implication in SARS-CoV-2 (COVID-19).|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883088|t=2020. Deducing the Crystal Structure of MERS-CoV Helicase.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883087|t=2020. Bacterial Artificial Chromosome-Based Lambda Red Recombination with the I-SceI Homing Endonuclease for Genetic Alteration of MERS-CoV.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883086|t=2020. Crystallization and Structural Determination of the Receptor-Binding Domain of MERS-CoV Spike Glycoprotein.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883085|t=2020. Biochemical Characterization of Middle East Respiratory Syndrome Coronavirus Spike Protein Proteolytic Processing.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883084|t=2020. Evaluating MERS-CoV Entry Pathways.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883083|t=2020. Studying Evolutionary Adaptation of MERS-CoV.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31144002|t=2020. Alphacoronavirus Detection in Lungs, Liver, and Intestines of Bats from Brazil.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31639467|t=2020. Immunohistochemical and molecular detection of natural cases of bovine rotavirus and coronavirus infection causing enteritis in dairy calves.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31982568|t=2020. Gga-miR-30d regulates infectious bronchitis virus infection by targeting USP47 in HD11 cells.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32011472|t=2020. Effect of isolation practice on the transmission of middle east respiratory syndrome coronavirus among hemodialysis patients: A 2-year prospective cohort study.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883095|t=2020. Development of a Mouse-Adapted MERS Coronavirus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883094|t=2020. Genetically Engineering a Susceptible Mouse Model for MERS-CoV-Induced Acute Respiratory Distress Syndrome.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883093|t=2020. Qualitative and Quantitative Determination of MERS-CoV S1-Specific Antibodies Using ELISA.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883092|t=2020. Generation of MERS-CoV Pseudotyped Viral Particles for the Evaluation of Neutralizing Antibodies in Mammalian Sera.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883091|t=2020. Evaluation of MERS-CoV Neutralizing Antibodies in Sera Using Live Virus Microneutralization Assay.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883090|t=2020. Quantification of the Middle East Respiratory Syndrome-Coronavirus RNA in Tissues by Quantitative Real-Time RT-PCR.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31883089|t=2020. Antigen Capture Enzyme-Linked Immunosorbent Assay for Detecting Middle East Respiratory Syndrome Coronavirus in Humans.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31279728|t=2020. Confronting the persisting threat of the Middle East respiratory syndrome to global health security.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31838832|t=2020. Middle East Respiratory Syndrome-Coronavirus Infection into Established hDPP4-Transgenic Mice Accelerates Lung Damage Via Activation of the Pro-Inflammatory Response and Pulmonary Fibrosis.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31838830|t=2020. Surface-Displayed Porcine IFN-lambda3 in Lactobacillus plantarum Inhibits Porcine Enteric Coronavirus Infection of Porcine Intestinal Epithelial Cells.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32785948|t=2020. How close is SARS-CoV-2 to canine and feline coronaviruses?|pdf=|usr=018}}
| + | |
| − | {{tp|p=32759577|t=2020. Role of cytotoxic T lymphocytes and interferon-gamma in coronavirus infection: lessons from murine coronavirus infections in mice.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32848107|t=2020. Clinical efficacy of combination therapy of itraconazole and prednisolone for treating effusive feline infectious peritonitis.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31940691|t=2020. Assessment of hemagglutination activity of porcine deltacoronavirus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31694947|t=2020. Three Amino Acid Changes in Avian Coronavirus Spike Protein Allow Binding to Kidney Tissue.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31694960|t=2020. Murine Coronavirus Infection Activates the Aryl Hydrocarbon Receptor in an Indoleamine 2,3-Dioxygenase-Independent Manner, Contributing to Cytokine Modulation and Proviral TCDD-Inducible-PARP Expression.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31801868|t=2020. Trypsin Treatment Unlocks Barrier for Zoonotic Bat Coronavirus Infection.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31776269|t=2020. Molecular Basis of Binding between Middle East Respiratory Syndrome Coronavirus and CD26 from Seven Bat Species.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31554686|t=2019. Broad Cross-Species Infection of Cultured Cells by Bat HKU2-Related Swine Acute Diarrhea Syndrome Coronavirus and Identification of Its Replication in Murine Dendritic Cells In Vivo Highlight Its Potential for Diverse Interspecies Transmission.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31534041|t=2019. The 3.1-Angstrom Cryo-electron Microscopy Structure of the Porcine Epidemic Diarrhea Virus Spike Protein in the Prefusion Conformation.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31534035|t=2019. Diversity of Dromedary Camel Coronavirus HKU23 in African Camels Revealed Multiple Recombination Events among Closely Related Betacoronaviruses of the Subgenus Embecovirus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31562757|t=2020. Activation of C-Type Lectin Receptor and (RIG)-I-Like Receptors Contributes to Proinflammatory Response in Middle East Respiratory Syndrome Coronavirus-Infected Macrophages.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32354534|t=2020. Demographic, clinical, and outcomes of confirmed cases of Middle East Respiratory Syndrome coronavirus (MERS-CoV) in Najran, Kingdom of Saudi Arabia (KSA); A retrospective record based study.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32307315|t=2020. The first clusters of Middle East respiratory syndrome coronavirus in Oman: Time to act.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31056437|t=2020. MERS-CoV infection among healthcare workers and risk factors for death: Retrospective analysis of all laboratory-confirmed cases reported to WHO from 2012 to 2 June 2018.|pdf=|usr=018}}
| + | |
| − | {{tp|p=30900940|t=2020. Preliminary investigation on feline coronavirus presence in the reproductive tract of the tom cat as a potential route of viral transmission.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31729897|t=2020. Feline coronavirus with and without spike gene mutations detected by real-time RT-PCRs in cats with feline infectious peritonitis.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31094626|t=2020. Effect of cat litters on feline coronavirus infection of cell culture and cats.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32720708|t=2020. Longitudinal epidemiology of human coronavirus OC43 in Yamagata, Japan, 2010-2017: Two groups based on spike gene appear one after another.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32720706|t=2020. More than just a common cold: Endemic coronaviruses OC43, HKU1, NL63, and 229E associated with severe acute respiratory infection and fatality cases among healthy adults.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31810359|t=2019. A Recombinant Influenza A/H1N1 Carrying A Short Immunogenic Peptide of MERS-CoV as Bivalent Vaccine in BALB/c Mice.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31861369|t=2019. Minimum Determinants of Transmissible Gastroenteritis Virus Enteric Tropism Are Located in the N-Terminus of Spike Protein.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31888266|t=2019. Endocytic Pathway of Feline Coronavirus for Cell Entry: Differences in Serotype-Dependent Viral Entry Pathway.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32150528|t=2020. Serologic Detection of Middle East Respiratory Syndrome Coronavirus Functional Antibodies.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31855530|t=2020. Diabetes Mellitus, Hypertension, and Death among 32 Patients with MERS-CoV Infection, Saudi Arabia.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31961300|t=2020. Middle East Respiratory Syndrome Coronavirus Transmission.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32223537|t=2020. Competing endogenous RNA network profiling reveals novel host dependency factors required for MERS-CoV propagation.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32090691|t=2020. Swine acute diarrhea syndrome coronavirus-induced apoptosis is caspase- and cyclophilin D- dependent.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32090689|t=2020. Trypsin promotes porcine deltacoronavirus mediating cell-to-cell fusion in a cell type-dependent manner.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31996093|t=2020. Discovery of a subgenotype of human coronavirus NL63 associated with severe lower respiratory tract infection in China, 2018.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31964246|t=2020. Polymorphisms in dipeptidyl peptidase 4 reduce host cell entry of Middle East respiratory syndrome coronavirus.|pdf=|usr=018}}
| + | |
| − | {{tp|p=31959375|t=2020. The risk factors associated with MERS-CoV patient fatality: A global survey.|pdf=|usr=018}}
| + | |
| − | {{tp|p=32604724|t=2020. Betacoronavirus Genomes: How Genomic Information has been Used to Deal with Past Outbreaks and the COVID-19 Pandemic.|pdf=|usr=011}}
| + | |
| − | {{tp|p=31859605|t=2020. Genetic manipulation of porcine deltacoronavirus reveals insights into NS6 and NS7 functions: a novel strategy for vaccine design |pdf=|usr=}}
| + | |
| − | {{tp|p=32186278|t=2020. Influenza-associated pneumonia as reference to assess seriousness of coronavirus disease (COVID-19) |pdf=|usr=}}
| + | |
| − | {{tp|p=32536567|t=2020. COVID-19 and Crimean-Congo Hemorrhagic Fever: Similarities and Differences.|pdf=|usr=011}}
| + | |
| − | {{tp|p=32556292|t=2020. COVID-19 and granulomatosis with polyangiitis (GPA): a diagnostic challenge.|pdf=|usr=010}}
| + | |
| − | {{tp|p=32370951|t=ä. Missed or Delayed Diagnosis of Kawasaki Disease During the 2019 Novel Coronavirus Disease (COVID-19) Pandemic |pdf=|usr=}}
| + | |
| − | {{tp|p=32341622|t=2020. SARS-CoV-2: Camazotz s Curse |pdf=|usr=}}
| + | |
| | {{tp|p=32246819|t=2020. Pulmonary High-Resolution Computed Tomography (HRCT) Findings of Patients with Early-Stage Coronavirus Disease 2019 (COVID-19) in Hangzhou, China |pdf=|usr=}} | | {{tp|p=32246819|t=2020. Pulmonary High-Resolution Computed Tomography (HRCT) Findings of Patients with Early-Stage Coronavirus Disease 2019 (COVID-19) in Hangzhou, China |pdf=|usr=}} |
| − | {{tp|p=32358574|t=ä. 100 years of influenza research seen through the lens of Covid-19 |pdf=|usr=}}
| |
| − | {{tp|p=32372197|t=ä. New challenges from Covid-19 pandemic: an unexpected opportunity to enlighten the link between viral infections and brain disorders?|pdf=|usr=}}
| |
| − | {{tp|p=32323862|t=2020. What can Parkinson s disease teach us about COVID-19?|pdf=|usr=}}
| |
| − | {{tp|p=30867314|t=2019. The Infectious Bronchitis Coronavirus Envelope Protein Alters Golgi pH To Protect the Spike Protein and Promote the Release of Infectious Virus.|pdf=|usr=011}}
| |
| − | {{tp|p=32342879|t=ä. COVID-19 and radiation induced pneumonitis: overlapping clinical features of different diseases |pdf=|usr=}}
| |
| − | {{tp|p=32202647|t=2020. Mimics and chameleons of COVID-19 |pdf=|usr=}}
| |
| − | {{tp|p=32184131|t=ä. Comparison of clinical characteristics of coronavirus disease (COVID-19) and severe acute respiratory syndrome (SARS) as experienced in Taiwan |pdf=|usr=}}
| |
| − | {{tp|p=32293833|t=2020. Emerging and reemerging respiratory viral infections up to Covid-19 |pdf=|usr=}}
| |
| − | {{tp|p=31670218|t=2020. Porcine deltacoronavirus (PDCoV) modulates calcium influx to favor viral replication |pdf=|usr=}}
| |
| − | {{tp|p=31936476|t=2020. Isolation and Identification of Porcine Deltacoronavirus and Alteration of Immunoglobulin Transport Receptors in the Intestinal Mucosa of PDCoV-Infected Piglets |pdf=|usr=}}
| |
| − | {{tp|p=30918070|t=2019. Identification and Characterization of a Human Coronavirus 229E Nonstructural Protein 8-Associated RNA 3'-Terminal Adenylyltransferase Activity.|pdf=|usr=011}}
| |
| | {{tp|p=32348692|t=2020. COVID-19 Related Genes in Sputum Cells in Asthma: Relationship to Demographic Features and Corticosteroids |pdf=|usr=}} | | {{tp|p=32348692|t=2020. COVID-19 Related Genes in Sputum Cells in Asthma: Relationship to Demographic Features and Corticosteroids |pdf=|usr=}} |
| − | {{tp|p=32374218|t=2020. Avian coronaviruses |pdf=|usr=}} | + | {{tp|p=32792041|t=2020. Hydroxychloroquine and Coronavirus Disease 2019: A Systematic Review of a Scientific Failure.|pdf=|usr=018}} |
| − | {{tp|p=32609845|t=2020. Influenza-induced thrombocytopenia is dependent on the subtype and sialoglycan receptor and increases with virus pathogenicity.|pdf=|usr=011}}
| + | {{tp|p=C7247491|t=?. Shedding ultraviolet light on coronavirus.|pdf=|usr=015}} |
| − | {{tp|p=32277530|t=ä. COVID?19 and SARS: Differences and similarities |pdf=|usr=}}
| + | {{tp|p=C7354272|t=2020. Modification of cellulose microfibers by polyglutamic acid and mesoporous silica nanoparticles for Enterovirus 71 adsorption.|pdf=|usr=015}} |
| − | {{tp|p=32522830|t=2020. Comparative pathogenesis of bovine and porcine respiratory coronaviruses in the animal host species and SARS-CoV-2 in humans.|pdf=|usr=011}}
| + | |
| − | {{tp|p=32319148|t=2020. COVID-19: searching for clues among other respiratory viruses |pdf=|usr=}}
| + | |
| − | {{tp|p=32237148|t=2020. Differences between COVID-19 and suspected then confirmed SARS-CoV-2-negative pneumonia: a retrospective study from a single center |pdf=|usr=}}
| + | |
| − | {{tp|p=32265517|t=2020. SARS-CoV-2 detection in patients with influenza-like illness |pdf=|usr=}}
| + | |
| − | {{tp|p=32287052|t=2020. Febrile Infant: COVID-19 in Addition to the Usual Suspects |pdf=|usr=}} | + | |
| − | {{ttp|p=32245885|t=2020. Learning from our immunological history: What can SARS-CoV teach us about SARS-CoV-2?|pdf=|usr=}}
| + | |
| − | {{tp|p=32358120|t=2020. How related is SARS-CoV-2 to other coronaviruses?|pdf=|usr=}}
| + | ---- |
| − | {{tp|p=15631713|t=2004. A preliminary investigation on the serological and epidemiological characteristics of severe acute respiratory syndrome in children |pdf=|usr=}}
| + | &pathomechanisms... endothelial topics went to pathobiology, thrombosis and renal. |
| − | {{tp|p=32198915|t=2020. When COVID-19 encounters interstitial lung disease: challenges and management |pdf=|usr=}}
| + | |
| − | {{tp|p=32133833|t=2020. The differential diagnosis of pulmonary infiltrates in cancer patients during the outbreak of the 2019 novel coronavirus disease |pdf=|usr=}} | + | personal opinion: |
| − | {{tp|p=32602823|t=2020. Bat SARS-Like WIV1 coronavirus uses the ACE2 of multiple animal species as receptor and evades IFITM3 restriction via TMPRSS2 activation of membrane fusion.|pdf=|usr=011}}
| + | |
| − | {{tp|p=32402576|t=ä. Oxidative Stress as Key Player in Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) Infection |pdf=|usr=}}
| + | part of the '''microangiopathic-hemolytic anemia / HELLP / SIH / HUS / TTP spectrum''' bc: |
| − | {{tp|p=25421478|t=2015. Biochemical Characterization of Recombinant Enterovirus 71 3C Protease with Fluorogenic Model Peptide Substrates and Development of a Biochemical Assay |pdf=|usr=}}
| + | |
| − | {{tp|p=24995382|t=2014. Accessory proteins of SARS-CoV and other coronaviruses |pdf=|usr=}}
| + | 1. micro/thromboembolism |
| − | {{ttp|p=23607598|t=2013. Involvement of high mobility group box 1 and the therapeutic effect of recombinant thrombomodulin in a mouse model of severe acute respiratory distress syndrome |pdf=|usr=}}
| + | 2. net's |
| − | {{tp|p=30461192|t=2019. Toward development of generic inhibitors against the 3C proteases of picornaviruses |pdf=|usr=}}
| + | 3. thrombocytopenia |
| − | {{tp|p=32574297|t=2020. Comparative Analysis of Early-Stage Clinical Features Between COVID-19 and Influenza A H1N1 Virus Pneumonia.|pdf=|usr=011}}
| + | 4. various neurological |
| − | {{tp|p=C7130142|t=ä. Tuberculosis and novel Wuhan coronavirus infection: Pathological interrelationship |pdf=|usr=}}
| + | 5. liver enzymes |
| − | {{tp|p=32387967|t=2020. A single centre study of viral community-acquired pneumonia in children: No evidence of SARS-CoV-2 from October 2019 to March 2020 |pdf=|usr=}}
| + | |
| − | {{ttp|p=17031779|t=2006. Expression of elevated levels of pro?inflammatory cytokines in SARS?CoV?infected ACE2+ cells in SARS patients: relation to the acute lung injury and pathogenesis of SARS? |pdf=|usr=}}
| + | data on vWF, adamts13, sflt3, vegf needed. |
| − | {{tp|p=15141376|t=2004. Organ distribution of severe acute respiratory syndrome (SARS) associated coronavirus (SARS?CoV) in SARS patients: implications for pathogenesis and virus transmission pathways |pdf=|usr=}}
| + | |
| − | {{tp|p=14743497|t=2004. Tissue and cellular tropism of the coronavirus associated with severe acute respiratory syndrome: an in?situ hybridization study of fatal cases |pdf=|usr=}}
| + | '''Infectious vasculitis''' |
| − | {{tp|p=12845623|t=2003. The clinical pathology of severe acute respiratory syndrome (SARS): a report from China |pdf=|usr=}}
| + | *''Kawasaki might be infectious or something transmitted by intercontinental aerosols...'' |
| − | {{tp|p=32387581|t=ä. EGFR Tyrosine Kinase Inhibitor?Associated Interstitial Lung Disease During the Coronavirus Disease 2019 Pandemic |pdf=|usr=}}
| + | *''Wegners responds to cotrim...'' |
| − | {{tp|p=32599823|t=2020. Host-Pathogen Responses to Pandemic Influenza H1N1pdm09 in a Human Respiratory Airway Model.|pdf=|usr=011}}
| + | *''NETosis is a pretty concept anything which triggers PMN...'' |
| − | {{tp|p=C7149537|t=2008. (mech resp)Severe Acute Respiratory Syndrome (SARS) |pdf=|usr=}}
| + | |
| − | {{tp|p=32145185|t=2020. Middle East respiratory syndrome |pdf=|usr=}}
| + | |
| − | {{tp|p=17142081|t=2007. Molecular pathogenesis of severe acute respiratory syndrome |pdf=|usr=}}
| + | |
| − | {{tp|p=28675506|t=2017. Determination of the cell tropism of serotype 1 feline infectious peritonitis virus using the spike affinity histochemistry in paraffin?embedded tissues |pdf=|usr=}}
| + | |
| − | {{tp|p=C7204879|t=2020. Human Coronavirus-229E, -OC43, -NL63, and -HKU1 |pdf=|usr=}}
| + | |
| − | {{tp|p=32397138|t=2020. A Systematic Review Analyzing the Prevalence and Circulation of Influenza Viruses in Swine Population Worldwide.|pdf=|usr=009}}
| + | |
| − | {{tp|p=23821437|t=2013. Activation of influenza viruses by proteases from host cells and bacteria in the human airway epithelium |pdf=|usr=}}
| + | |
| − | {{tp|p=15127935|t=2003. Prediction of amino acid pairs sensitive to mutations in the spike protein from SARS related coronavirus |pdf=|usr=}}
| + | |
| − | {{tp|p=15306390|t=2004. Viral evolution and the emergence of SARS coronavirus |pdf=|usr=}}
| + | |
| − | {{tp|p=31541590|t=2020. Pathogenicity of porcine deltacoronavirus (PDCoV) strain NH and immunization of pregnant sows with an inactivated PDCoV vaccine protects 5?day?old neonatal piglets from virulent challenge |pdf=|usr=}}
| + | |
| − | {{tp|p=30520548|t=2019. Co?localization of Middle East respiratory syndrome coronavirus (MERS?CoV) and dipeptidyl peptidase?4 in the respiratory tract and lymphoid tissues of pigs and llamas |pdf=|usr=}}
| + | |
| − | {{tp|p=32035270|t=ä. Fatal human coronavirus 229E (HCoV-229E) and RSV?Related pneumonia in an AIDS patient from Colombia |pdf=|usr=}}
| + | |
| − | {{tp|p=15381196|t=2004. Cellular entry of the SARS coronavirus |pdf=|usr=}}
| + | |
| − | {{tp|p=15833113|t=2005. Molecular advances in the cell biology of SARS-CoV and current disease prevention strategies |pdf=|usr=}}
| + | |
| − | {{tp|p=16690096|t=2006. Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |pdf=|usr=}}
| + | |
| − | {{tp|p=16678878|t=2006. Induction of protective immunity against severe acute respiratory syndrome coronavirus (SARS-CoV) infection using highly attenuated recombinant vaccinia virus DIs |pdf=|usr=}}
| + | |
| − | {{tp|p=32482591|t=2020. Swine enteric alphacoronavirus (swine acute diarrhea syndrome coronavirus): An update three years after its discovery.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32503352|t=2020. Genomic Sequencing and Analysis of Eight Camel-Derived Middle East Respiratory Syndrome Coronavirus (MERS-CoV) Isolates in Saudi Arabia.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32461317|t=2020. Porcine Deltacoronavirus nsp5 Cleaves DCP1A to Decrease Its Antiviral Ability.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32407507|t=2020. Genomic epidemiology, evolution, and transmission dynamics of porcine deltacoronavirus.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32461321|t=2020. Porcine epidemic diarrhea virus deficient in RNA cap guanine-N-7 methylation is attenuated and induces higher type I and III interferon responses.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32241072|t=2020. [Comparison of clinical and pathological features between severe acute respiratory syndrome and coronavirus disease 2019].|pdf=|usr=007}}
| + | |
| − | {{tp|p=32502331|t=2020. Comparison of confirmed COVID-19 with SARS and MERS cases - Clinical characteristics, laboratory findings, radiographic signs and outcomes: A systematic review and meta-analysis.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32418550|t=2020. Are Iranian Sulfur Mustard Gas-Exposed Survivors More Vulnerable to SARS-CoV-2? Some Similarity in Their Pathogenesis.|pdf=|usr=007}}
| + | |
| − | {{tp|p=32398299|t=2020. To compare the incomparable: COVID-19 pneumonia and high altitude disease.|pdf=|usr=008}}
| + | |
| − | {{tp|p=32437766|t=2020. Multivesicular bodies mimicking SARS-CoV-2 in patients without COVID-19.|pdf=|usr=009}}
| + | |
| − | {{tp|p=32392945|t=2020. [Comparison of pathological changes and pathogenic mechanisms caused by H1N1 influenza virus, highly pathogenic H5N1 avian influenza virus, SARS-CoV, MERS-CoV and 2019-nCoV].|pdf=|usr=007}}
| + | |
| − | {{tp|p=32360499|t=2020. Comparative seasonalities of influenza A, B and 'common cold' coronaviruses - setting the scene for SARS-CoV-2 infections and possible unexpected host immune interactions.|pdf=|usr=008}}
| + | |
| − | {{tp|p=32053148|t=2020. Three Emerging Coronaviruses in Two Decades.|pdf=|usr=008}}
| + | |
&pathomechanisms... endothelial topics went to pathobiology, thrombosis and renal.
1. micro/thromboembolism
2. net's
3. thrombocytopenia
4. various neurological
5. liver enzymes
