Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mohamed Baaj"'
Autor:
Ghizlane Zoulati, Ramatou Yèya Maïga, Ouafae El Abdallaoui, Fatima El Boukhrissi, Ali Zinebi, Houssine Balouch, Mohamed Baaj, Youssef Bamou
Publikováno v:
Cahiers Santé Médecine thérapeutique. 30:131-135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f84782fc337df8675e7c0f0445aa513
https://doi.org/10.1684/sanmt.2021.24
https://doi.org/10.1684/sanmt.2021.24
Publikováno v:
Néphrologie & Thérapeutique. 6:52-56
We report a case of 36-year-old woman, admitted for hypotonic tetraparesis. Laboratory tests revealed severe hypokalaemia, acidosis, hyperchloremia and alkaline urinary pH allowing the diagnosis of distal tubular acidosis. Additional investigations l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15d92b365d9e02494ff6da5825017c57
https://doi.org/10.1016/j.nephro.2009.09.002
https://doi.org/10.1016/j.nephro.2009.09.002
Autor:
Fatima El Boukhrissi, Mohamed El Haouri, Salma Benjelloun, Hazar Lahlou, Moncef Amrani Hassani, Ghita Yahyaoui, Imane Tlamçani, Youssef Bamou, Mohamed Karim Moudden, L. Balouch, Mohamed Baaj
Publikováno v:
Annales de biologie clinique. 72(4)
Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b20042e3770cd948129fa0ff9fcf18
https://pubmed.ncbi.nlm.nih.gov/25119807
https://pubmed.ncbi.nlm.nih.gov/25119807
Publikováno v:
La Presse Médicale. 38:1194-1196
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3db27a3ba44629efbdaf62ca3eb3e40f
https://doi.org/10.1016/j.lpm.2008.04.016
https://doi.org/10.1016/j.lpm.2008.04.016
Publikováno v:
Revue du Rhumatisme. 75:292-294
Resume Le syndrome de Buschke–Ollendorff (SBO) est une affection autosomique dominante associant un hamartome de type elastique et une osteopœcilie. Observation Une jeune femme âgee de 21 ans est atteinte de syndrome de Buschke–Ollendorff revel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfefbd92357b5f95a776cad7a847f328
https://doi.org/10.1016/j.rhum.2007.04.018
https://doi.org/10.1016/j.rhum.2007.04.018
Publikováno v:
Joint Bone Spine. 75:212-214
Buschke–Ollendorff syndrome (BOS) is an autosomal dominant disorder characterized by elastin-rich hamartomas and osteopoikilosis. Case report In a 21-year-old woman, osteopoikilosis led to the diagnosis of BOS. She had multiple, grouped, buff-color
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04a27ab9975f482e3172da28533d8ed2
https://doi.org/10.1016/j.jbspin.2007.04.027
https://doi.org/10.1016/j.jbspin.2007.04.027
Publikováno v:
Revue du Rhumatisme. 74:899-901
Resume L'association syndrome de Sweet et maladie de Behcet est peu rapportee dans la litterature. Observation Une femme âgee de 47 ans aux antecedents d'aphtose bipolaire recidivante negligee depuis cinq ans. Elle fut hospitalisee pour des lesions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bd9497488e3e89ee41b10801700108d
https://doi.org/10.1016/j.rhum.2006.11.033
https://doi.org/10.1016/j.rhum.2006.11.033
Autor:
Abdelhamid Naitlhou, Mohamed Baaj, Hasna Hassikou, Fatima Tabache, Yahya Cherrah, Abdeslam El Kartouti, Abdelilah Tarib
Publikováno v:
Joint bone spine. 78(3)
Joint Bone Spine - In Press.Proof corrected by the author Available online since dimanche 27 mars 2011
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc4e2664fed48eaf587f1ec047e87ec8
https://pubmed.ncbi.nlm.nih.gov/22115587
https://pubmed.ncbi.nlm.nih.gov/22115587
Publikováno v:
Nephrologietherapeutique. 6(1)
We report a case of 36-year-old woman, admitted for hypotonic tetraparesis. Laboratory tests revealed severe hypokalaemia, acidosis, hyperchloremia and alkaline urinary pH allowing the diagnosis of distal tubular acidosis. Additional investigations l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a53cf5b554ac1ce8df33e4d7d5e692a
https://pubmed.ncbi.nlm.nih.gov/19836323
https://pubmed.ncbi.nlm.nih.gov/19836323
Publikováno v:
Presse medicale (Paris, France : 1983). 38(7-8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf0a7f6bec38acad9421323a674d8ac5
https://pubmed.ncbi.nlm.nih.gov/19167186
https://pubmed.ncbi.nlm.nih.gov/19167186