Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mouna, Lehlimi"'
Autor:
Luis A. Méndez-Rosado, Norma de León-Ojeda, Alina García, Frenny Sheth, Asmaa Gaadi, Ahmed Aziz Bousfiha, Mouna Lehlimi, Abdelhafid Natiq, Oxana S. Kurinnaia, Svetlana G. Vorsanova, Ivan Iourov, Dagmar Huhle, Thomas Liehr
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-8 (2022)
Abstract Background DiGeorge syndrome (DGS), caused by a deletion del(22)(q11.2q11.2), is the most frequently observed microdeletion syndrome. There is a vast clinical heterogeneity in DGS, and several studies suggested also heterogeneity of clinical
Externí odkaz:
https://doaj.org/article/1d14f5e89b2c49e4aece3d936bbec468
Publikováno v:
Clinical dysmorphology. 32(1)
Publikováno v:
Journal de Pédiatrie et de Puériculture. 34:36-43
Resume Introduction La maladie hemolytique Rhesus du nouveau-ne resulte de l’alloimmunisation des globules rouges maternels contre les antigenes des globules rouges pour lesquels la mere et le fœtus sont incompatibles. L’IFM Rhesus peut conduire
Autor:
Abdu El Karim sylla, Mouna Lehlimi, Aamal Badre, Salima Hajjaji, Soukaina Lyazidi, Sanaa Ameayou, Mounir Chemsi, Abdourahman Habzi, Said Benomar, Samira Nani, Samira Hassoune
Objective: This study aimed to estimate the prevalence and identify the associated factors of breastfeeding (BF) practice in the NICU of Casablanca Ibn Rochd teaching hospital.Method: A cross-sectional study was performed between 04 January and 26 Ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc295845d9cf0f1fa7f0ab945672e98b
https://doi.org/10.21203/rs.3.rs-1522715/v1
https://doi.org/10.21203/rs.3.rs-1522715/v1
Autor:
Néhémie, Nzoyikorera, Mouna, Lehlimi, Idrissa, Diawara, Khalid, Zerouali, Raja, Alami, Khalid, Katfy, Fakhreddine, Maaloum, Mounir, Chemsia, Abderahim, Habzi, Said, Benomar, Naima, Elmdaghri
Publikováno v:
African health sciences. 21(4)
A male late preterm newborn was born by vaginal delivery at a gestational age of 34 weeks. At 3 hours of life, he was admitted for early moderate neonatal respiratory distress in the Neonatal Medicine and Resuscitation Service. Cerebrospinal fluid cu
Publikováno v:
Journal de Pédiatrie et de Puériculture. 33:151-157
Resume L’incompatibilite fœto-maternelle dans le systeme ABO est la plus frequente des incompatibilites erythrocytaires fœto-maternelles. Le but de cette etude est de decrire les caracteristiques : epidemiologiques, cliniques, biologiques et ther
Publikováno v:
Périnatalité. 13:43-45
Le syndrome de Kasabach-Merritt (SKM) est une affection rare et grave qui associe une lésion vasculaire (hémangiome), un syndrome hématologique dominé par une thrombopénie, souvent profonde, exposant à un syndrome hémorragique et une coagulopa
Publikováno v:
La Presse Médicale. 45:605-607
La Presse Medicale - In Press.Proof corrected by the author Available online since samedi 14 mai 2016
Autor:
Said Benomar, S. Houari, Mounir Chemsi, Abderrahim Habzi, Mouna Lehlimi, H. Hamid, Khalid Zerouali, M. Ouhadous
Publikováno v:
Journal of Infectious Diseases & Therapy.
In september 2013, an outbreak of Serratiamarcescens infection occured in the neonatal intensive care unit of children’s hospital Abderrahim Harrouchi in Casablanca. Rapid microbiological investigation lead to identify nine cases of S. marcescens s