Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Ayad Ghanam"'
Autor:
Hassnae Tkak, MD, Ayad Ghanam, PhD, Mohamed Belahcen, PhD, Imane Kamaoui, PhD, Amal Bennani, PhD, Nadir Myri, MD, Aziza Elouali, PhD, Maria Rkain, PhD, Abdeladim Babakhouya, PhD, Noufissa Benajiba, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 3508-3511 (2024)
Rhabdomyosarcoma is a malignant tumor in children that might mimic a benign tumor, such as infantile hemangioma, particularly when detected early. Although rhabdomyosarcoma rarely occurs in the hand, its prognosis is generally poor, and successful tr
Externí odkaz:
https://doaj.org/article/1df551428b0847119b54e60a2760d6ee
Autor:
Aziza Elouali, Soulaimane M'harzi, Karim Lahrache, Ayad Ghanam, Abdeladim Babakhouya, Maria Rkain, Noufissa Benajiba
Publikováno v:
Leukemia Research Reports, Vol 20, Iss , Pp 100375- (2023)
Externí odkaz:
https://doaj.org/article/7dabb5aff9654242aec1e97a1a63924d
Autor:
Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, Ayad Ghanam, Manal Elidrissi Errahhali, Zaina Sidqi, Meryem Ouarzane, Majida Charif, Mohammed Bellaoui, Redouane Boulouiz, Noufissa Benajiba
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background β‐thalassemia syndromes are the most common hereditary blood disorders in the world and are recognized as a major health problem in Morocco. They are characterized by the reduction or the absence of β‐globin chain synthesis.
Externí odkaz:
https://doaj.org/article/7432a49777244b6db0d2ee805064a31f
Autor:
M'harzi Soulaimane, Aziza Elouali, Younesse Najioui, Ayad Ghanam, Maria Rkain, Abdeladim Babakhoya, Najat Lamalmi, Amal Bennani, Noufissa Benajiba
Publikováno v:
Journal of Clinical and Translational Endocrinology Case Reports, Vol 24, Iss , Pp 100111- (2022)
Unbalanced diabetes can lead to many complications related to insulin deficiency. Hepatocytic glycogenic overload, formerly known as Mauriac syndrome, is one of them. It is a rare syndrome initially described in children with type 1 diabetes (T1D) wh
Externí odkaz:
https://doaj.org/article/311deb970bb8434dbc0f4b838187050a
Autor:
Soulaimane M'harzi, Aziza Elouali, Karim Lahrache, Ayad Ghanam, Abdeladim Babakhouya, Maria Rkain, Noufissa Benajiba
Publikováno v:
Leukemia Research Reports, Vol 18, Iss , Pp 100357- (2022)
Acute lymphoblastic leukemia (ALL) is the most frequent malignancy in children,representing 25–30% of all childhood malignancies. Although treatment outcome has improved owing to advances in chemotherapy, there is still a group of patients who expe
Externí odkaz:
https://doaj.org/article/6529182c94474a7a94f4e69a94a424d9
Autor:
Ayad Ghanam, Aziza Elouali, Merouane Nour, Maria Rkain, Noufissa Benajiba, Abdeladim Babakhouya
Publikováno v:
Case Reports in Pediatrics, Vol 2022 (2022)
Bean syndrome (BS) or blue rubber bleb nevus syndrome is a rare clinical entity characterized by venous malformations mainly in the skin and digestive tract, whose hemorrhagic complications can be life threatening. We report a case of Bean syndrome i
Externí odkaz:
https://doaj.org/article/0c6a212b3ffa45b5817bf441ce19737d
Autor:
Zohair El Haddar, Aziza El Ouali, Ayad Ghanam, Maria Rkain, Noufissa Benajiba, Abdeladim Babakhouya
Publikováno v:
Case Reports in Pediatrics, Vol 2021 (2021)
Kawasaki disease (KD) is a vasculitis mostly seen in children aged less than 5 years. It can involve different organs and tissues. Its diagnosis is based on the clinical criteria of the American Heart Association (AHA). We report a case of a Moroccan
Externí odkaz:
https://doaj.org/article/9f49ed4945bb4251826623ca01c7c520
Autor:
Sara Anane, Hajar Boudarbala, Ayad Ghanam, Amal Bennani, Houssain Benhaddou, Imane Kamaoui, Noufissa Benajiba
Publikováno v:
OALib. 10:1-4
Autor:
Hajar Boudarbala, Sara Anane, Nadia Bouhafs, Abdeladim Babakhouya, Ayad Ghanam, Aziza Elouali, Maria Rkain, Noufissa Benajiba
Publikováno v:
OALib. 10:1-5
Autor:
Mariem Labrahimi, Madiha Benhachem, Aziza Elouali, Ayad Ghanam, Maria Rkain, Abdeladim Babakhouya
Publikováno v:
OALib. 10:1-4