Zobrazeno 1 - 7
of 7
pro vyhledávání: '"SAMIRA EL MACHTANI IDRISSI"'
Autor:
Asmâa Biaz, Mohammed Drissi, Aissam El Maataoui, Samira El Machtani Idrissi, Sanae Bouhsain, Abdellah Dami, Abdellatif Boulahya, Zohra Ouzzif
Publikováno v:
The Pan African Medical Journal, Vol 29, Iss 40 (2018)
INTRODUCTION: L'objectif de cette étude prospective, réalisée sur une année au laboratoire de biochimie de l'HMIMV de Rabat, vise à étudier la cinétique de la Troponine Ic (TnIc) après chirurgie cardiaque sous circulation extracorporelle (CEC
Externí odkaz:
https://doaj.org/article/b31779584afe4b098078d2b038adc6e0
Autor:
Asmea Biaz, Maroua Neji, Yousra Ajhoun, Samira EL Machtani Idrissi, Abdellah Dami, Karim Reda, Zohra Ouzzif, Sanae Bouhsain
Publikováno v:
The Pan African Medical Journal, Vol 27, Iss 93 (2017)
Le syndrome drépanocytaire composite SC représente 20% à 30% des syndromes drépanocytaires majeurs. Nous rapportons le cas d'une découverte fortuite d'une drépanocytose hétérozygote composite SC dans un contexte de décollement rétinien. Il
Externí odkaz:
https://doaj.org/article/bd24584339c14372ace888aef8d29b0a
Autor:
Zhor Ouzzif, KAMAL DOGHMI, nezha messaoudi, Sanae Bouhsain, SAMIRA EL MACHTANI IDRISSI, Asmâa Biaz, Achraf Rachid, Abdellah Dami, Ahmed BEZZA, AISSAM EL MAATAOUI
Introduction: Monoclonal gammopathies are a group of disorders associated with monoclonal proliferation of plasma cells that produces a monoclonal protein. To describe the epidemiological and immunochemical characteristics of monoclonal gammopathies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4098f22e22e153958182be989daf75c0
https://doi.org/10.22541/au.166662723.34466136/v1
https://doi.org/10.22541/au.166662723.34466136/v1
Autor:
Abdellah Dami, Samira El-Machtani-Idrissi, Asmaa Biaz, Sanae Bouhsain, Jalila Zirar, Naoufal Hjira, Elmehdi Elouadani
Publikováno v:
Clinical Laboratory. 67
Background We report a case of pseudo-hyperchloremia in a patient hospitalized in the dermatology department at the Mohammed V Military Hospital of Instruction in Rabat. The examination revealed self-medication with calcium bromo-galactogluconate, al
Autor:
Mohammed Chemsi, Asmaa Biaz, Samira El Machtani-Idrissi, Sophia Tazi, Sanae Bouhsain, Abdellah Dami
Publikováno v:
Clinical Laboratory. 66
Hereditary xanthinuria was the first inherited purine metabolism disorder described. It is a rare pathology, which is most often asymptomatic and whose incidence is therefore underestimated. We report the case of a patient with an undetectable level
Autor:
Sanae Bouhsain, Christelle M Fataki, Abdellah Dami, Don Carleone S Bagadema, Samira El Machtani-Idrissi, Driss El Kabbaj, Fakhita Lazreq, Asmaa Biaz
Publikováno v:
Clinical Laboratory. 66
Background We report a case of a multiple myeloma with light polymerized kappa chains, a phenomenon rarely described. Methods Capillary electrophoresis of serum proteins (Capillarys 2 Flex Piercing Sebia ®) revealed the presence of two migrant monoc
Better Resolution of Gel Electrophoresis than that of Capillary Electrophoresis: About a Case Report
Autor:
Ghizlane El-Amin, Zohra Ouzzif, Samira El-Machtani-Idrissi, Jean Uwingabiye, Sanae Bouhsain, Chaimae Raiss, Abdellah Dami, Asmâa Biaz
Publikováno v:
Clinical Laboratory. 65