Results 1 to 10 of about 5,456,377 (265)

Post-acute COVID-19 syndrome

open access: yesNature Medicine, 2021
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the pathogen responsible for the coronavirus disease 2019 (COVID-19) pandemic, which has resulted in global healthcare crises and strained health resources.
Ani Nalbandian   +33 more
semanticscholar   +1 more source

The GoodHope Ehlers Danlos Syndrome Clinic: development and implementation of the first interdisciplinary program for multi-system issues in connective tissue disorders at the Toronto General Hospital

open access: yesOrphanet Journal of Rare Diseases, 2021
Ehlers-Danlos Syndrome (EDS) are a heterogeneous group of genetic connective tissue disorders, and typically manifests as weak joints that subluxate/dislocate, stretchy and/or fragile skin, organ/systems dysfunction, and significant widespread pain ...
Nimish Mittal   +25 more
doaj   +1 more source

The species Severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2

open access: yesNature Microbiology, 2020
The present outbreak of a coronavirus-associated acute respiratory disease called coronavirus disease 19 (COVID-19) is the third documented spillover of an animal coronavirus to humans in only two decades that has resulted in a major epidemic.
Alexander E. Susan C. Ralph S. Raoul J. Christian Anastasia Gorbalenya Baker Baric de Groot Drosten Gulyaeva H   +17 more
semanticscholar   +1 more source

RETRACTED ARTICLE: Targeting transforming growth factor beta (TGF-β) using Pirfenidone, a potential repurposing therapeutic strategy in colorectal cancer

open access: yesScientific Reports, 2023
The modulating factors within the tumor microenvironment, for example, transforming growth factor beta (TGF-β), may limit the response to chemo and immunotherapy protocols in colorectal cancer (CRC).
Hamid Jamialahmadi   +17 more
doaj   +1 more source

Pathological findings of COVID-19 associated with acute respiratory distress syndrome

open access: yesThe Lancet Respiratory Medicine, 2020
Treatment and Research Center for Infectious Diseases (Z Xu MD, L Shi MD, J Zhang PhD, L Huang MD, C Zhang PhD, P Zhao MSc, H Liu BSc, J Song PhD, P Xia MSc, Prof F-S Wang MD), Department of Pathology and Hepatology (Y Wang PhD, S Liu MSc, L Zhu MSc ...
Zhe Xu   +17 more
semanticscholar   +1 more source

A Synopsis of the Evidence for the Science and Clinical Management of Cardiovascular-Kidney-Metabolic (CKM) Syndrome: A Scientific Statement From the American Heart Association

open access: yesCirculation, 2023
A growing appreciation of the pathophysiological interrelatedness of metabolic risk factors such as obesity and diabetes, chronic kidney disease, and cardiovascular disease has led to the conceptualization of cardiovascular-kidney-metabolic syndrome. The
C. Ndumele   +28 more
semanticscholar   +1 more source

Utility of the EULAR Sjögren syndrome disease activity index in Japanese children: a retrospective multicenter cohort study

open access: yesPediatric Rheumatology Online Journal, 2020
Background The European League Against Rheumatism (EULAR) Sjögren Syndrome Disease Activity Index (ESSDAI) has been utilized to assess Sjögren syndrome-related systemic involvement in adult patients. To date, however, the ESSDAI has not been validated in
Naomi Iwata   +10 more
doaj   +1 more source

Primary breast angiosarcoma in postmenopausal women with a picture like Kasabach-Merritt syndrome: A case report [PDF]

open access: yesVojnosanitetski Pregled, 2021
Introduction. Primary breast angiosarcoma is a very rare tumor and accounts for 0.04% of all breast malignant tumors and most commonly occur in young women.
Ćuk Mirjana   +5 more
doaj   +1 more source

Dental Management of Prader-Willi Syndrome in a 7-year-old Girl: A Rare Case Report [PDF]

open access: yesJournal of South Asian Association of Pediatric Dentistry, 2022
Prader-Willi syndrome (PWS) is a rare genetic disorder characterized by a lack of expression of paternal genes located on chromosome 15q11-q13. Prader-Willi syndrome is characterized by hypothalamic dysfunction.
Mallayya C Hiremath   +4 more
doaj   +1 more source

Intracerebral haemorrhage in Down syndrome: protected or predisposed? [version 1; referees: 2 approved]

open access: yesF1000Research, 2016
Down syndrome (DS), which arises from trisomy of chromosome 21, is associated with deposition of large amounts of amyloid within the central nervous system.
Lewis Buss   +6 more
doaj   +1 more source

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