Zobrazeno 1 - 10
of 63
pro vyhledávání: '"B Chkirate"'
Publikováno v:
Asian Journal of Pediatric Research. :39-45
Introduction: Digestive involvement is not uncommon during chronic inflammatory diseases in children, it may be just digestive manifestations other than other systemic signs or association of two different pathologies with a common immunological terr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::597062e936983c23ca7c74759765827a
https://doi.org/10.9734/ajpr/2022/v10i1189
https://doi.org/10.9734/ajpr/2022/v10i1189
Publikováno v:
Journal de Pédiatrie et de Puériculture. 33:198-201
Resume Les manifestations digestives dans le purpura rhumatoide n’ont aucune specificite. Elles peuvent etre banales a type de vomissements ou de douleurs abdominales ou mimer un syndrome chirurgical abdominal aigu, voire engager le pronostic vital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::963ba9fad7e4cc3b7ce312436f58f53d
https://doi.org/10.1016/j.jpp.2020.04.003
https://doi.org/10.1016/j.jpp.2020.04.003
Akademický článek
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Autor:
B. Chkirate, Hanane Elouardi, Grégory Egéa, Laure Raymond, Mohamed Taoudi, Said El Mouatassim, Abdelali Zrhidri, Jaber Lyahyai, Saadia Amasdl, Abdelaziz Sefiani
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 15, Iss 1, Pp 1-6 (2017)
Pediatric Rheumatology Online Journal, Vol 15, Iss 1, Pp 1-1 (2017)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology
Pediatric Rheumatology Online Journal, Vol 15, Iss 1, Pp 1-1 (2017)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology
Background Scleroderma is a multisystem disease, characterized by fibrosis of skin and internal organs, immune dysregulation, and vasculopathy. The etiology of the disease remains unknown, but it is likely multifactorial. However, the genetic basis f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5047e1c19590d882e6d34d87fa121940
http://link.springer.com/article/10.1186/s12969-017-0200-2
http://link.springer.com/article/10.1186/s12969-017-0200-2
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-4 (2018)
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-4 (2018)
Background Familial Mediterranean fever is an autoinflammatory disease of unknown etiology, characterized clinically by recurrent attacks of sudden-onset fever with arthralgia and/or thoracoabdominal pain and pathogenetically by autosomal recessive i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41cb396d1a6b700125fbd94978acaa0c
https://doi.org/10.1186/s13256-017-1552-4
https://doi.org/10.1186/s13256-017-1552-4
Autor:
I. Bouaddi, Najia Hajjaj-Hassouni, B. Chkirate, Samira Rostom, Bouchra Amine, D. El Badri, A. Hassani
Publikováno v:
Rheumatology International. 34:665-668
Abnormal puberty is often reported in children suffering from many chronic diseases. Juvenile idiopathic arthritis (JIA) is the most common joint disorder in developing children. The aim of this study was to assess sexual maturation of Moroccan child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8bb675d203fc16a92d3e2fc56886785
https://doi.org/10.1007/s00296-013-2737-9
https://doi.org/10.1007/s00296-013-2737-9
Publikováno v:
Pediatric Rheumatology Online Journal
Behcet disease is a systemic vascularitis, the diagnosis is difficult in child. The most frequent ocular signs in child is panuveitis with retinian vascularitis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811b29256f588da141aeac4c982e4a00
https://doi.org/10.1186/1546-0096-12-s1-p235
https://doi.org/10.1186/1546-0096-12-s1-p235
Autor:
A. Hassani, B. Chkirate, Samira Rostom, Bouchra Amine, I. Bouaddi, D. Badri, Najia Hajjaj-Hassouni
Publikováno v:
The Pan African Medical Journal, Vol 17, Iss 115 (2014)
The Pan African Medical Journal
The Pan African Medical Journal
Introduction The link between bone mass and body composition is widely recognized, but only few works were selectively performed on subjects with juvenile idiopathic arthritis. The aim of our study was to investigate the effect of body composition on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::124c36b77a9af5633e6991a4f4adf31e
https://doi.org/10.11604/pamj.2014.17.115.1838
https://doi.org/10.11604/pamj.2014.17.115.1838
Autor:
Samira Rostom, Bouchra Amine, I. Bouaddi, B. Chkirate, A. Hassani, D. El Badri, Najia Hajjaj-Hassouni
Publikováno v:
Journal of Arthritis.
Aim: The aim of this study was to evaluate the bone mineral density (BMD) in Moroccan patients with juvenile idiopathic arthritis and its correlates with disease parameters and vitamin D status. Methods: Forty patients with juvenile idiopathic arthri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93d381902f5c941dc4c03bbac10d03c5
https://doi.org/10.4172/2167-7921.1000131
https://doi.org/10.4172/2167-7921.1000131
Autor:
A. Bentahila, B. Chkirate, F. Jabourik, A. Rouichi, H. Ait Ouamar, A. Gaouzi, A. Mouhid Belhadj
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 50:279-284
Resume L'anomalie de naissance de la coronaire gauche a partir de l'artere pulmonaire est une cardiopathie congenitale rare, mais grave. Elle est souvent responsable d'une insuffisance cardiaque par ischemie myocardique des les premiers mois de la vi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b509352cd85da6ee1ab53076034aa46
https://doi.org/10.1016/s0003-3928(01)00027-0
https://doi.org/10.1016/s0003-3928(01)00027-0