Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Amal Naous MD"'
Autor:
Amal Naous, MD, Walaa Ghannoum, MD, Aya Abbas, MBBCh, Hussein Darwish, MBBCh, Zeina Naja, MD, Mariam Rajab, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5124-5127 (2024)
The coronavirus disease 2019 (COVID-19) pandemic that was spread worldwide since 2019 and showed a highly contagious character affecting the lifestyle of people worldwide causing symptoms that are not limited to the respiratory system only but had mu
Externí odkaz:
https://doaj.org/article/4d2e3022fc244239bddaa9b3bb9443a7
Surgical management of congenital pouch colon in Lebanon: A case report and review of the literature
Autor:
Amal Naous, MD, Christin Berjaoui, Medical Students, Malek Osta, Medical Students, Amar Hafez, MD, Khaldoun Sinno, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4208-4212 (2024)
Congenital pouch colon (CPC) is a rare congenital abnormality, in which a pouch-like dilatation partially or completely replaces the colon, creating a fistula with the urogenital. Congenital colonic pouch is an extremely rare congenital disease mainl
Externí odkaz:
https://doaj.org/article/dd77bfdfc0734ce7827560a0a6eb73d1
Publikováno v:
Radiology Case Reports, Vol 19, Iss 2, Pp 737-740 (2024)
Throughout the literature, many pathologic lung lesions and complications following coronavirus disease 2019 (COVID-19) infection have been reported including pneumatocele formation which could potentially lead to pneumothorax development. This case
Externí odkaz:
https://doaj.org/article/9c3e08c838984a5286e20f1b2aa738e9
Publikováno v:
Radiology Case Reports, Vol 19, Iss 2, Pp 499-502 (2024)
Diseases of the gastrointestinal system may be congenital or acquired. Intestinal obstruction is common in children and neonates, and it has various causes. Obstructions due to congenital adhesion bands are rare. Few cases were reported in the litera
Externí odkaz:
https://doaj.org/article/1125c976812e427aa6cbdaadaaf9c703
Autor:
Amal Naous MD, Abdel Rahman Shatila MD, Zeina Naja MD, Ahmad Salaheddine Naja MD, Mariam Rajab MD
Publikováno v:
Child Neurology Open, Vol 2 (2015)
Encephalocraniocutaneous lipomatosis or Haberland syndrome is a rare, congenital neurocutaneous syndrome. It is characterized by unilateral lipomatous hamartomata of the scalp, eyelid, and outer globe of the eye and ipsilateral neurologic malformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::cff397a3223f820acc5cf1749450b00f
https://doaj.org/article/01d3e5e32aec4e69a313dfdac31ef381
https://doaj.org/article/01d3e5e32aec4e69a313dfdac31ef381