Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mahdi Parvizi, Mashhadi"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Intestinal atresia and hirschsprung disease are two common causes of bowel obstruction in neonates; simultaneous occurrence is rare. This report delineates a 36‐week newborn with ileal atresia and total colonic hirschsprung who was referre
Externí odkaz:
https://doaj.org/article/62443828105740c294a69fd81086ae6c
Autor:
Hojjat Shadman Zahroodi, Mehran Monazzami, Paria Dehghanian, Leila Ameri, Pegah Bahrami Taqanaki, Mahdi Parvizi Mashhadi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 90, Iss , Pp 102581- (2023)
Background: Benign vascular tumors that can be found anywhere in the body are defined as hemangiomas The most common clinical manifestation is gastrointestinal bleeding (GIB). Other possible signs and symptoms could be Iron deficiency anemia, intesti
Externí odkaz:
https://doaj.org/article/82612592ace149889f7a41ce9d8b97ae
Publikováno v:
Journal of Cardio-Thoracic Medicine, Vol 9, Iss 4, Pp 899-904 (2021)
Introduction: Maintaining a vascular access is a common procedure in neonates specifically for those who need prolonged hospitalization or intensive care support. This situation may happen several times among those with complex congenital anomalies t
Externí odkaz:
https://doaj.org/article/c6d6e2dfaf0f41bfbbe1da295d4b9830
Autor:
Hamzeh sherafati, Marjan Joodi, Mehdi Fathi, Mohammad Aref Emami, Leila Ameri, Pegah Bahrami Taqanaki, Mohammad Mehdi Zarif Soltani, Alireza Ghodsi, Mahdi Parvizi Mashhadi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 79, Iss , Pp 102231- (2022)
Insulinoma is an extremely rare pancreatic neuroendocrine tumor that originates from insulin-secreting islet cells, with an incidence of one to four cases per million each year. Here, we report a case of a 16-year-old boy presenting with seizures who
Externí odkaz:
https://doaj.org/article/ec763d084cd74783aab61b38879ae638
Autor:
Mahdi Parvizi Mashhadi, Mehdi Fathi, Mohammad Mehdi Zarif soltani, Alireza Ghodsi, Marjan Joodi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 72, Iss , Pp 101827- (2021)
Midline cervical cleft is an extremely rare congenital anomaly of the anterior neck, which accounts for 1.7–2% of congenital neck malformations. Here, we report a case of an 18-month-old boy with congenital midline cervical cleft who was successful
Externí odkaz:
https://doaj.org/article/c028f9680da649f4ae59652c510da4c2
Autor:
Mehdi Fathi, Mahdi Parvizi Mashhadi, Alireza Sabzevari, Mohammad Mehdi Zarif soltani, Alireza Ghodsi, Marjan Joodi
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 68, Iss , Pp 101841- (2021)
Circumcision is one of the most common surgical operations, which is usually a safe and simple procedure with rare complications. Amputation of glans is an uncommon condition but has definitive risk of complication. It's crucial to consider patients
Externí odkaz:
https://doaj.org/article/4c8ae67e904e403f871a36ea295b95fb
Autor:
Ramin, Sadeghi, Reza, Shojaeian, Mehran, Hiradfar, Ahmad, Mohammadipour, Ali, Azadmand, Mahdi Parvizi, Mashhadi
Publikováno v:
Journal of Pediatric Surgery. 57:1518-1522
Although the sentinel lymph node Biopsy (SLNB) is well stablished in solid tumors among adults but the experience on SLNB in pediatrics is still limited. In this article we report our experience of sentinel lymph node detection that is applied on ped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29ef4e88096284997aef80444e0460a9
https://doi.org/10.1016/j.jpedsurg.2021.12.037
https://doi.org/10.1016/j.jpedsurg.2021.12.037
Publikováno v:
Annals of Medicine & Surgery.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eef367d7a0a7e94822300373bc577eff
https://doi.org/10.1097/ms9.0000000000000691
https://doi.org/10.1097/ms9.0000000000000691
Intestinal atresia and Hirschsprung disease are two common causes of bowel obstruction in neonates,simultaneous occurrence is rare. This report delineates a 36-week newborn with ileal atresia and total colonic Hirschsprung who was referred to our uni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44ca078c3ec7e31c47b2414a7bb5b262
https://doi.org/10.22541/au.166766944.47455458/v1
https://doi.org/10.22541/au.166766944.47455458/v1
Intestinal atresia and Hirschsprung disease are two common causes of bowel obstruction in neonates, and simultaneous occurrence is rare. This report delineates a 36-week newborn with ileal atresia and total colonic Hirschsprung. A newborn male (gesta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06b62bcecdcbc66962adbd920649e7fc
https://doi.org/10.21203/rs.3.rs-1875233/v1
https://doi.org/10.21203/rs.3.rs-1875233/v1