Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Imane Tlamçani"'
Publikováno v:
Cahiers Santé - Médecine Thérapeutique; may/jun2024, Vol. 33 Issue 3, p169-172, 4p
Autor:
null Imane Tlamçani, null Zineb Azzine, null Hanae Kaaouch, null Ouahiba Bhallil, null Moncef Amrani Hassani
Publikováno v:
International Journal of Life Science Research Archive. 4:047-051
Introduction: The discovery of hemolytic anemia must lead to a precise etiological assessment guided by clinical and biological data. The aim of our study is to describe the etiological profile of hemolytic anemia cases diagnosed in the hematology la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::094a7644e2c2e1f7c505c24802ddea4a
https://doi.org/10.53771/ijlsra.2023.4.2.0055
https://doi.org/10.53771/ijlsra.2023.4.2.0055
Autor:
Imane Benbella, Jihade Elamouri, Khalil Lemhouer, Zineb Azzine, Fatima Zahra Benatiya, Fatima Elboukhrissi, Imane Tlamçani, Mustapha Mahmoud
Publikováno v:
Saudi Journal of Medicine. 8:135-139
Primary plasma cell leukemia (pPCL) is a rare lymphoproliferative disease characterized by a malignant proliferation of plasma cells in the bone marrow and peripheral blood. It is either primary (in 60% of cases) or a secondary complication of multip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e36caac62362fca1f283170bb81caa3f
https://doi.org/10.36348/sjm.2023.v08i04.001
https://doi.org/10.36348/sjm.2023.v08i04.001
Autor:
Ghita Yahyaoui, Salma Benjelloun, Moncef Hassani Amrani, Mohammed Karim Moudden, Imane Tlamçani, Najoua Benseddik, Meryem Alami, Mohamed El Baaj, Mohammed Er-rami
Publikováno v:
Journal of Microbiology and Infectious Diseases, Vol 4, Iss 2, Pp 44-49 (2014)
Volume: 4, Issue: 02 44-49
Journal of Microbiology and Infectious Diseases
Volume: 4, Issue: 02 44-49
Journal of Microbiology and Infectious Diseases
Objective: To evaluate the importance of imported malaria at the Moulay Ismail Military Hospital of Meknes, we have led a descriptive study of the epidemiological, clinical, biological and evolutionary characteristics of the registered malaria case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaaf70a4a23df0af7215c0a76f3a61ba
http://jmidonline.org/upload/sayi/17/JMID-00753.pdf
http://jmidonline.org/upload/sayi/17/JMID-00753.pdf
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
Autor:
Mohamed Karim Moudden, Salma Benjelloun, Mohamed El Baaj, Moncef Hassani Amrani, Youssef Bamou, Fatima El Boukhrissi, Imane Tlamçani, L. Balouch, Najoua Benseddik, Ghita Yahyaoui
Publikováno v:
Annales de biologie clinique. 72(2)
Waldenstrom disease is a rare hematologic disorder characterized by lymphoplasmacytic proliferation associated with the production of monoclonal IgM. Visceral injuries are described but some are rare (lung), others never reported (cardiac). We report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7db2f444be1c9236a04ce3beeaf00d
https://pubmed.ncbi.nlm.nih.gov/24736145
https://pubmed.ncbi.nlm.nih.gov/24736145
Publikováno v:
The Pan African Medical Journal, Vol 17, Iss 93 (2014)
Nous rapportons le cas d'une aspergillose pulmonaire chronique necrosante chez un patient tabagique et ancien tuberculeux. Le diagnostic a ete base sur des criteres radiologiques, tomodensitometriques et mycologiques. Le champignon a ete isole des cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42acc01bcdb9465be694d54a34f35d3c
https://doaj.org/article/22c85cd173a74c289915cddaa622d205
https://doaj.org/article/22c85cd173a74c289915cddaa622d205
Publikováno v:
The Pan African Medical Journal
La leucémie aigue érythroblastique (LAM-M6) est une entité rare, représente 3 à 4% de l'ensemble des leucémies aigues. Il en existe deux types: l’érythroleucémie et la leucémie érythroïde pure. Elle se manifeste le plus souvent par des s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::819d37a527746eacbbad9f84321fa01f
https://pubmed.ncbi.nlm.nih.gov/26113895
https://pubmed.ncbi.nlm.nih.gov/26113895
Publikováno v:
The Pan African Medical Journal, Vol 18, Iss 61 (2014)
La leucémie aigue érythroblastique (LAM-M6) est une entité rare, représente 3 à 4% de l'ensemble des leucémies aigues. Il en existe deux types : l'érythroleucémie et la leucémie érythroïde pure. Elle se manifeste le plus souvent par des si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcda829fa68f661fa4fa15d527a9a9a9
https://doi.org/10.11604/pamj.2014.18.61.3921
https://doi.org/10.11604/pamj.2014.18.61.3921