Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hajar Andour MD"'
Autor:
Amine Naggar MD, Saad Assila MD, Khadija Laasri MD, Hajar Andour MD, Zineb Izi MD, Najat Lamalmi PhD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 11 (2024)
Nephrogenic rests (NRs) are foci of embryonic nephrogenic cells that persist beyond the 36th week of gestation. They are precursor lesions of Wilms tumor and are found incidentally in approximately 1% of infants. The term nephroblastomatosis (NBS) is
Externí odkaz:
https://doaj.org/article/5fb2e0a0f8de4c62b57fb951123ea890
Autor:
Amine Naggar MD, Hajar Andour MD, Hamza Bensaghir MD, Badr Kabila MD, Chaimae Ben Driss MD, Soukaina El Aouni MD, Monim Ochan PhD, Mounir Kisra PhD, Najat Lamalmi PhD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Mesenchymal hamartoma (MH) is a benign liver tumor accounting for 3% to 8% of all liver tumors in children, commonly manifesting before 3 years of life. Distinguishing MH from hepatoblastoma and other liver tumors relies on imaging and alpha-fetoprot
Externí odkaz:
https://doaj.org/article/a1397d4ede634b2ab4b4471a3de15c0e
Autor:
Amine Cherraqi MD, Siham El Haddad MD PhD, Ola Messaoud MD, Hajar Andour MD, Mohammed Tbouda MD, Naoual El Ansari MD, Amina KILI MD PhD, Laila Hessissen MD PhD, Nazik Allali MD PhD, Latifa Chat MD PhD
Publikováno v:
Global Pediatric Health, Vol 10 (2023)
Schwannomas are uncommon benign tumors of the peripheral nerves with a low risk of malignant transformation. They rarely affect children, can affect any part of the body but rarely occur in the lower extremity and typically present with a palpable ma
Externí odkaz:
https://doaj.org/article/8244910ea8a748b58c7bf8fb87ddf9a9
Autor:
Amine Cherraqi, MD, Kaoutar Imrani, MD, Hajar Andour, MD, Ola Messaoud, MD, Khadija Benelhosni, MD, Nabil Moatassim Billah, MD, PhD, Ittimade Nassar, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 1, Pp 11-16 (2023)
Low phospholipid-associated cholelithiasis (LPAC) is a rare, still poorly understood genetic disorder characterized by the association of an ABCB4 mutation and low biliary phospholipid concentration with recurrent cholelithiasis, responsible for the
Externí odkaz:
https://doaj.org/article/ec0cb6fda690400699932048dd4a480f
Autor:
Chirihan Ayadi, MD, Safae Lanjery, MD, Hajar Andour, MD, Farah Kamel, MD, Hamza El Qandili, MD, Mendes Papys, MD, Laila Jroundi, MD, Fatima Zahra Laamrani, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 11, Pp 4239-4243 (2022)
Brown tumors are benign bone tumors that rarely complicate hyperparathyroidism, manifesting as fibrous and erosive lesions secondary to rapid and localized osteoclast turnover. These lesions are typical of primary hyperparathyroidism, but they are no
Externí odkaz:
https://doaj.org/article/c06fcc3f8332460b9e22b54e7cee165e
Autor:
Hajar Andour, MD, Amine Cheraqui, MD, Amal Lahfidi, MD, Meriem Fikri, PhD, Najwa Ech-cherif el kettani, PhD, Mohamed Jiddane, PhD, Firdaous Touarsa, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 2, Pp 545-549 (2023)
Posterior reversible encephalopathy syndrome (PRES) is an uncommon, but important, pathology affecting primarily the posterior cerebral circulation. Typical imaging features include vasogenic edema involving the bilateral occipital and parietal lobes
Externí odkaz:
https://doaj.org/article/5fb30def373d40c1823c976178013084