questionsmedicales.fr
Régions géographiques
Océanie
Australasie
Australasie : Questions médicales fréquentes
Termes MeSH sélectionnés :
DNA Copy Number Variations
Diagnostic
5
Maladies tropicales
Diagnostic médical
Paludisme
Tests de diagnostic
Virus Zika
Infections virales
Maladie de Lyme
Diagnostic médical
Symptômes
5
Virus de l'herpès
Infections virales
Intoxication alimentaire
Symptômes
Infections respiratoires
Symptômes
Prévention
5
Infections respiratoires
Prévention
Traitements
5
Maladie de Lyme
Traitements
Complications
5
Chikungunya
Complications
Leptospirose
Complications
Maladie de Lyme
Complications
Facteurs de risque
5
Dengue
Facteurs de risque
Chikungunya
Facteurs de risque
Virus Zika
Facteurs de risque
Leptospirose
Facteurs de risque
Maladie de Lyme
Facteurs de risque
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"text": "Éliminer les eaux stagnantes et utiliser des répulsifs contre les moustiques."
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"position": 12,
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"position": 21,
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"text": "Des douleurs articulaires chroniques peuvent persister longtemps après l'infection."
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"position": 23,
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"acceptedAnswer": {
"@type": "Answer",
"text": "Les personnes travaillant en milieu rural ou en contact avec des eaux contaminées sont à risque."
}
},
{
"@type": "Question",
"name": "Qui est à risque pour la maladie de Lyme ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les personnes vivant dans des zones boisées ou ayant des activités de plein air sont à risque."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 17/04/2025
Contenu vérifié selon les dernières recommandations médicales
12 publications dans cette catégorie
5 publications dans cette catégorie
Affiliations :
Faculty of Medicine and Health, Sydney School of Public Health, Sydney Health Ethics, The University of Sydney, Sydney, NSW, Australia.
Publications dans "Australasie" :
5 publications dans cette catégorie
Affiliations :
Imperial Clinical Trials Unit, Imperial College London, Stadium House, 68 Wood Lane, London, UK.
Publications dans "Australasie" :
5 publications dans cette catégorie
Affiliations :
Imperial Clinical Trials Unit, Imperial College London, Stadium House, 68 Wood Lane, London, UK.
Publications dans "Australasie" :
5 publications dans cette catégorie
Affiliations :
Imperial Clinical Trials Unit, Imperial College London, Stadium House, 68 Wood Lane, London, UK.
Publications dans "Australasie" :
4 publications dans cette catégorie
Affiliations :
Hunter Genetics, Waratah, NSW, Australia.
Publications dans "Australasie" :
4 publications dans cette catégorie
Affiliations :
International Union of Phlebology (UIP), Chatswood, NSW, Australia.
Australasian College of Phlebology (ACP), Chatswood, NSW, Australia.
Publications dans "Australasie" :
4 publications dans cette catégorie
Affiliations :
International Union of Phlebology (UIP), Chatswood, NSW, Australia.
European College of Phlebology (ECoP), Rotterdam, The Netherlands.
Publications dans "Australasie" :
4 publications dans cette catégorie
Affiliations :
550809American Venous Forum (AVF), East Dundee, IL, USA.
Publications dans "Australasie" :
4 publications dans cette catégorie
Affiliations :
550809American Venous Forum (AVF), East Dundee, IL, USA.
Publications dans "Australasie" :
4 publications dans cette catégorie
Affiliations :
Australasian College of Phlebology (ACP), Chatswood, NSW, Australia.
Interventional Radiology Society of Australasia (IRSA), Ultimo, NSW, Australia.
Publications dans "Australasie" :
3 publications dans cette catégorie
Affiliations :
Genetic Counseling, Graduate School of Health, University of Technology Sydney, Sydney, New South Wales, Australia.
Publications dans "Australasie" :
3 publications dans cette catégorie
Affiliations :
Melbourne Law School, University of Melbourne, Melbourne, VIC, Australia.
Biomedical Ethics Research Group, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Publications dans "Australasie" :
3 publications dans cette catégorie
Affiliations :
Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
Melbourne Genomics Health Alliance, Melbourne, VIC, Australia.
Australian Genomics Health Alliance, Melbourne, VIC, Australia.
Publications dans "Australasie" :
3 publications dans cette catégorie
Affiliations :
Department of Clinical Research, Dobney Hypertension Centre, School of Medicine, Royal Perth Hospital Unit, University of Western Australia, Level 3, MRF Building, Rear 50 Murray St, Perth, WA MDBP M570, Australia.
Publications dans "Australasie" :
2 publications dans cette catégorie
Affiliations :
Australasian Institute of Digital Health, Australia.
Publications dans "Australasie" :
2 publications dans cette catégorie
Affiliations :
Australasian Institute of Digital Health, Australia.
University of Technology Sydney, Australia.
Publications dans "Australasie" :
2 publications dans cette catégorie
Affiliations :
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
Publications dans "Australasie" :
2 publications dans cette catégorie
Affiliations :
Department of Biomedical and Clinical Sciences L. Sacco, Università degli Studi di Milano, Milan, Italy.
Publications dans "Australasie" :
2 publications dans cette catégorie
Affiliations :
School of Medicine, Deakin University, Geelong, Australia.
Publications dans "Australasie" :
In this review we discuss epigenetic disorders that result from aberrations in genes linked to epigenetic regulation. We describe current testing methods for the detection of copy number variants (CNV...
The purpose of this review is to summarize recent findings on copy number variations and susceptibility to osteoporosis....
Osteoporosis is highly influenced by genetic factors, including copy number variations (CNVs). The development and accessibility of whole genome sequencing methods has accelerated the study of CNVs an...
Schizophrenia is a neurodevelopmental disorder with genetic and environmental factors involved in its aetiology. Genetic liability contributing to the development of schizophrenia is a subject of exte...
Embryonic chromosomal abnormalities represent a major causative factor in early pregnancy loss, highlighting the importance of understanding their role in spontaneous abortion. This study investigates...
We analyzed Copy Number Variations (CNVs) in 395 aborted fetal specimens from spontaneous abortion patients by CNV-seq. And collected correlated data, including maternal age, gestational week, and Bod...
Out of the 395 cases, 67.09% of the fetuses had chromosomal abnormalities, including numerical abnormalities, structural abnormalities, and mosaicisms. Maternal age was found to be an important risk f...
Overall, these findings provide important insights into the understanding of spontaneous abortion and have implications for the development of personalized interventions for patients with abnormal kar...
Quantitative PCR (qPCR) is used for the determination of gene copy number (GCN). GCNs contribute to human disorders, and characterize copy number variation (CNV). The single laboratory method validati...
Neuropsychiatric disorders are complex conditions that represent a significant global health burden with complex and multifactorial etiologies. Technological advances in recent years have improved our...
Inherited copy number variations (CNVs) can provide valuable information for cancer susceptibility and prognosis. However, their association with oropharynx squamous cell carcinoma (OPSCC) is still po...
Identification of a unique genomic biomarker in de novo inflammatory breast cancer (IBC) may provide an insight into the biology of this aggressive disease. The goal of our study was to elucidate biom...
Genomic copy-number variants (CNVs) contribute to as many congenital heart disease (CHD) cases (10-15%) as chromosomal aberrations or single-gene mutations and influence clinical outcomes. CNVs in a f...
Craniofacial osteosarcomas (CFOS) are uncommon malignant neoplasms of the head and neck with different clinical presentation, biological behavior and prognosis from conventional osteosarcomas of long ...
In the current study, we performed comprehensive genomic studies in 15 cases of high-grade CFOS by SNP array and targeted next generation sequencing....
Our study shows high-grade CFOS demonstrate highly complex and heterogenous genomic alterations and harbor frequently mutated tumor suppressor genes TP53, CDKN2A/B, and PTEN, similar to conventional o...
High-grade CFOS demonstrate highly complex and heterogenous genomic alterations, with amplification involving receptor tyrosine kinase genes, and frequent mutations involving tumor suppressor genes....