Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Zohra, Ouzzif"'
Autor:
Zohra Ouzzif, Kamal Doghmi, Nezha Messaoudi, Sanae Bouhsain, Samira El Machtani, Asmae Biaz, Achraf Rachid, Abdallah Dami, Ahmed Bezza, Aissam El Maataoui
Publikováno v:
Cancer Reports, Vol 6, Iss 5, Pp n/a-n/a (2023)
Abstract Background Monoclonal gammopathies are a group of disorders associated with clonal proliferation of plasma cells that produces a monoclonal protein. Aims The main objective of this study was to describe the epidemiological and immunochemical
Externí odkaz:
https://doaj.org/article/523bd0f47bce45cebb9dd83cb056a9d9
Influence of homocysteine and its major genetic and nutritional determinants on bone mineral density
Publikováno v:
La Tunisie medicale. 100(7)
A potential role of hyperhomocysteinemia in bone metabolism has been considered from the observation of high prevalence of osteoporosis in subjects with homocystinuria about 50 years ago.To examine the association of homocysteine level and its determ
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
Publikováno v:
Annales de biologie clinique. 78(1)
Hemoglobin D-Punjab is a common hemoglobin variant in India but very rare in Morocco. Often, its presence has minimal or no clinical impact. Its heterozygous association with β-thalassemia is exceptional. The purpose of the study is to describe the
Autor:
Zohra Ouzzif, Aissam El Maataoui
Publikováno v:
Clinical Reviews in Bone and Mineral Metabolism. 16:67-73
Even though the North African countries are located in one of the sunniest place in the world, several North African studies from there proved a high prevalence of hypovitaminosis D in men and women. The objectives of the present review are to summar
Autor:
Samira Elmachatni Idrissi, Badia Belarj, Jean Uwingabiye, Zohra Ouzzif, Asmae Biaz, Souhail Dahraoui, Sanae Bouhsain, Achraf Rachid, Abdellah Dami
Publikováno v:
Clinical Case Reports
Key Clinical Message We report the case of multiple myeloma of unexpected discovery in an old patient admitted to the emergency department of cardiomyopathy. This observation emphasizes the need for exploring any anemia before linking it to heart fai
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
Autor:
Jean Uwingabiye, Asmâa Biaz, Elmostafa Benaissa, Zohra Ouzzif, Emmanuel Millbank Owusu, S. Idrissi, Sanae Bouhsain, Abdellah Dami
Publikováno v:
Clinical Laboratory. 65
BACKGROUND The authors report a clinical case where biological interference rendered the electrophoretic trace of serum proteins obtained by capillary electrophoresis as uninterpretable. METHODS Electrophoresis of serum proteins and immunotyping immu
Autor:
Zohra Ouzzif, Souhail Dahraoui, Emmanuel Millbank Owusu, Anas Rochdi, Nawfel Doghmi, Sanae Bouhsain, Jean Uwingabiye, Asmaa Biaz, Abdellah Dami, Badia Belarj, Amine El Alaoui, S. Idrissi
Publikováno v:
Clinical Case Reports
Light‐chain multiple myeloma is a malignant hemopathy characterized by medullary invasion by tumor plasma cells, with the secretion of free light chains of immunoglobulins in the blood giving signs of bone disorders. However, it can be asymptomatic