Zobrazeno 1 - 10
of 43
pro vyhledávání: '"C Dahou-Makhloufi"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Rheumatology. 61
Background Dermatomyositis (DM) is an inflammatory myopathy that is often severe and affects children (juvenile DM) in 50% of cases. Subcutaneous calcinosis is seen in 30–70% of juvenile DM and often poses a problem in terms of treatment. We report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5aa8aa02abe03553c2bd025a9aeefa73
https://doi.org/10.1093/rheumatology/keac496.042
https://doi.org/10.1093/rheumatology/keac496.042
Publikováno v:
Rheumatology. 61
Background Systemic scleroderma (SSc) is a rare generalized connective tissue disorder of poorly understood aetiology resulting in systemic fibrosis. It affects mainly women, usually in adulthood, but can occur at any age, although it is rare in chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85d13c298756539113300c01bb484d27
https://doi.org/10.1093/rheumatology/keac496.071
https://doi.org/10.1093/rheumatology/keac496.071
Publikováno v:
Rheumatology. 61
Background Spinal pain is a frequent symptom whose aetiology can be extremely varied. It is not only the prerogative of adults; it is frequent in children and particularly in adolescents. Inflammatory spinal pain is a warning sign that should prompt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94b4bc30c355470324897b42f77cd200
https://doi.org/10.1093/rheumatology/keac496.058
https://doi.org/10.1093/rheumatology/keac496.058
Publikováno v:
Rheumatology. 61
Background Osteogenesis imperfecta, or “glass bone disease”, is a rare genetic disorder due to an abnormality in the production of type 1 collagen. It is characterised by bone fragility and low bone mass, leading to repeated fractures. Osteogenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c66ea7cdc44899b569f3bb406c35c40
https://doi.org/10.1093/rheumatology/keac496.072
https://doi.org/10.1093/rheumatology/keac496.072
Publikováno v:
Rheumatology. 61
Background Spondyloarthritis is a heterogeneous group of chronic inflammatory rheumatism, of which enthesitis is the most common. Achilles involvement is frequent and can be disabling, resisting various treatments (non-steroidal anti-inflammatory dru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4abeeadb1857adc1f955663e9bfc036f
https://doi.org/10.1093/rheumatology/keac496.034
https://doi.org/10.1093/rheumatology/keac496.034
Publikováno v:
Rheumatology. 61
Background Juvenile idiopathic arthritis (JIA) is a group of inflammatory joint diseases that begin before the age of 16. Depending on the clinical form of JIA, medical treatment may involve long-term high-dose corticosteroid therapy, which may lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88e2b9969a92e9cdfdc8205737668ad9
https://doi.org/10.1093/rheumatology/keac496.004
https://doi.org/10.1093/rheumatology/keac496.004
Publikováno v:
Rheumatology. 60
Background Camptodactyly, arthropathy, coxa vara, pericarditis (CACP) syndrome is a rare genetic disorder with autosomal recessive transmission including camptodactyly, synovial hyperplasia-related arthropathy, progressive coxa vara deformity and non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95d3ccb9874ab01b2d79a896132b1fb8
https://doi.org/10.1093/rheumatology/keab722.087
https://doi.org/10.1093/rheumatology/keab722.087
Publikováno v:
Rheumatology. 60
Background Juvenile idiopathic arthritis (JIA) is a heterogeneous group of rare conditions that begin before the age of 16. Seven categories have been defined by the International League of Associations for Rheumatology (ILAR) classification. The aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20bbc51270ded3449d94a1cebdb356f1
https://doi.org/10.1093/rheumatology/keab722.031
https://doi.org/10.1093/rheumatology/keab722.031
Autor:
S. Hashad, L. El Kibbi, S. Abu Al Saoud, M. Daou, Nelly Ziade, Basel Masri, Bassel Elzorkany, I. Frase, C. Dahou-Makhloufi, Wafa Hamdi, S. Saad, K. Al Naqbi, Hussein Halabi, Mervat Eissa, S. AlEmadi, R. Niamane, F. Abutiban, M. el Rakawi, Ihsane Hmamouchi, L. Kazkaz, N. Abdullateef
Publikováno v:
Rheumatology International
BackgroundTelehealth use is increasing and will undeniably continue to play a role beyond the COVID-19 era. Best practice guidelines (BPG) for telehealth add credibility, standardize approaches, facilitate reimbursement, and decrease liability.Object
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52515e29e80dd285858f6d8872cdde79
https://pubmed.ncbi.nlm.nih.gov/34993578
https://pubmed.ncbi.nlm.nih.gov/34993578