Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Mohamed Hbibi"'
Autor:
Meriem Haloua, MD, Nizar El Bouardi, MD, Mohamed Hbibi, MD, Badre Eddine Alami, MD, Youssef Alaoui Lamrani, MD, Nawal Hammas, MD, Mustapha Maaroufi, MD, Youssef Bouabdallah, MD, Meryeme Boubbou, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3825-3829 (2022)
We report the case of a 2.5-year-old child admitted for abdominal distension, whose imaging revealed a large posterior mediastinal cystic mass, with a tissue component, a calcification, and a minimal fat component. The ultrasound- guided biopsy led t
Externí odkaz:
https://doaj.org/article/6d75dcd66ab741529138055a0514022f
Autor:
Meriem Haloua, assistant professor, Nizar El Bouardi, assistant professor, Mohamed Hbibi, associate Professor, Badre Eddine Alami, associate Professor, Youssef Alaoui Lamrani, associate Professor, Mustapha Maaroufi, professor of higher education, Meryeme Boubbou, professor of higher education
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 3015-3018 (2022)
Primary intracranial germ cell tumors are rare, often affecting children and young patients. Germinomas are the most common type of germ cell tumors. We present the case of a 10-year-old child, who was admitted with decreased visual acuity, asthenia,
Externí odkaz:
https://doaj.org/article/39ab5787ed1645808dc00911b72a5758
Autor:
Mohamed Hbibi, Sara Benmil, Safae Rahmouni, Ilhame Tadmouri, Sana Abourazzak, Sana Chaouki, Fatima Zahra Souilmi, Mounia Lakhdar Idrissi, Mostapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 31, Iss 74 (2018)
Le syndrome d'activation macrophagique (SAM) est une atteinte multisystémique, liée à une intense activation du système immunitaire correspondant à une infiltration plus ou moins diffuse des tissus par des macrophages activés. Il associé des s
Externí odkaz:
https://doaj.org/article/b412de57a4a640e4b22eb20561b9b098
Autor:
Jaouad El Maghraoui, Fatima Zahrae Souilmi, Mohamed Hbibi, Tarik Sqalli Houssaini, Mustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 425 (2015)
La néphrocalcinose se définit par la présence anormale dans le parenchyme rénal de dépôts calciques pouvant résulter de différentes affections. Nous rapportons le cas d'un nourrisson de 7 mois chez qui nous avons diagnostiqué une hypercalcé
Externí odkaz:
https://doaj.org/article/a98ebde7ed8b40458f0e3b96c0f13cd5
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 3 (2015)
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal re
Externí odkaz:
https://doaj.org/article/1e01905510a24508a6c227fc09efdd23
Publikováno v:
Case Reports in Pediatrics, Vol 2014 (2014)
Hemophagocytic lymphohistiocytosis (HLH) is a severe life-threatening disorder, responsible for extensive phagocytosis of hematopoietic cells and causing a multisystem organ failure. If lymphomas are common causes of HLH, the association with Hodgkin
Externí odkaz:
https://doaj.org/article/417cf19a49414fcd9e37f0de0e06a9a2
Autor:
Karim Ouldim, Imane Samri, Laila Bouguenouch, Hasna Hamdaoui, Ihsan El Otmani, Mohamed Hbibi, Sana Chaouki, Moustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 11, Iss 4 (2012)
Le syndrome du Cri du Chat (Cri du Chat syndrome, CdCS) est une anomalie chromosomique résultant d'une délétion de taille variable de l'extrémité du bras court du chromosome 5 (5p), incluant une région critique située en p15.2. Il représente
Externí odkaz:
https://doaj.org/article/878185ee9606404a9eb32644b7f1b780
Publikováno v:
Pan African Medical Journal. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8112f73dd5f4bc7e240dc86dea5b6d67
https://doi.org/10.11604/pamj.2023.44.99.29037
https://doi.org/10.11604/pamj.2023.44.99.29037
Autor:
Abderrahmane Moundir, Hind Ouair, Ibtihal Benhsaien, Leila Jeddane, Nouredine Rada, Naïma Amenzoui, Zineb Jouhadi, Fatima Adnane, Naïma El Hafidi, Amina Kili, Asmaa Bourhanbour Drissi, Abdeladim Babakhouya, Sarra Benmiloud, Mohamed Hbibi, Noufissa Benajiba, Mustapha Hida, Mohamed Bouskraoui, Chafiq Mahraoui, Brahim Admou, Jalila El Bakkouri, Fatima Ailal, Ahmed Aziz Bousfiha
Publikováno v:
Journal of clinical immunology.
Genetic testing provides great support to validate the clinical diagnosis of inborn errors of immunity (IEI). However, the high cost and advanced technology make these tests inaccessible to a large proportion of patients in low-income countries. In t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb714acf741771e0f1e1900f232f8dc
https://pubmed.ncbi.nlm.nih.gov/36367635
https://pubmed.ncbi.nlm.nih.gov/36367635
Publikováno v:
Trauma International. 6:15-17
Osteobalstoma is a benign primary bone tumor which represents 3% of all benign tumors and 1% of all bone tumors. It is localized commonly in the spine. We report the case of a 5 year-old boy with cervicothoracic spine osteoblastoma. The incidence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d21f92db366d20bbff671e46c34787f5
https://doi.org/10.13107/ti.2020.v06i02.106
https://doi.org/10.13107/ti.2020.v06i02.106