Results 1 to 10 of about 5,596,228 (313)
Orphanet 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
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Scientific 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
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Pediatric 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
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Primary breast angiosarcoma in postmenopausal women with a picture like Kasabach-Merritt syndrome: A case report [PDF]
Vojnosanitetski 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
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Dental Management of Prader-Willi Syndrome in a 7-year-old Girl: A Rare Case Report [PDF]
Journal 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
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Parent and self-report health-related quality of life measures in young patients with Tourette syndrome [PDF]
, 2012 Tourette syndrome is a neurodevelopmental disorder characterized by tics and comorbid behavioral problems. This study compared child- and parent-reported quality of life and everyday functioning.
Balottin, U +11 more
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Optimized real-time fluorescence PCR assay for the detection of porcine Circovirus type 3 (PCV3)
BMC Veterinary Research, 2020 Background Porcine circovirus type 3 (PCV3) has been an emerging porcine virus spread around the world. The conserved DNA sequence of PCV3 enabled good performance in molecular biological assays.
Lin Yuan +9 more
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Comparison of resting-state EEG between adults with Down syndrome and typically developing controls
Journal of Neurodevelopmental Disorders, 2021 Background Down syndrome (DS) is the most common genetic cause of intellectual disability (ID) worldwide. Understanding electrophysiological characteristics associated with DS provides potential mechanistic insights into ID, helping inform biomarkers and
Sarah Hamburg +3 more
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Prevalence of metabolic syndrome in baluch women in Chabahar [PDF]
, 2015 Epidemiological studies have shown the importance of the metabolic syndrome. With estimation of the metabolic syndrome, it may predict cardiovascular disease, sudden death and the presence of some other cardiovascular risk factors.
Majidi, F. +4 more
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The myocardial and coronary histopathology and pathogenesis of hypoplastic left heart syndrome [PDF]
, 2015 Hypoplastic left heart syndrome has the greatest mortality rate among all CHDs and without palliation is uniformly fatal. Despite noble efforts, the aetiology of this syndrome is unknown and a cure remains elusive.
Cole, Charles R, Eghtesady, Pirooz
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