Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Rachida, Laamiri"'
Autor:
Amina Chaka, Amine Fredj Daassa, Wadye Hamdouni, Kamel Ktari, Rachida Laamiri, Abdellatif Nouri
Publikováno v:
African Journal of Urology, Vol 27, Iss 1, Pp 1-7 (2021)
Abstract Background Testicular microlithiasis in children was defined for the first time in 1961 based on histological criteria. There should be more than 5 calcifications per testicle in order to say that the patient has testicular microlithiasis. I
Externí odkaz:
https://doaj.org/article/3cec44c6c39c4b3d85b695ead33719b4
Autor:
Rachida Laamiri, Sahla Sellami, Nahla Kechiche, Mabrouk Abdelaali, Mongi Mekki, Mohsen Belghith
Publikováno v:
Egyptian Liver Journal, Vol 11, Iss 1, Pp 1-4 (2021)
Abstract Background Intrathoracic rupture of hepatic hydatid cyst is a rare but dangerous complication. Its occurrence in children is exceptional as diagnosis and management constitute real challenges. We report two cases of intrathoracic rupture of
Externí odkaz:
https://doaj.org/article/a9ac7cb28f814f7da5d07daba81be3f0
Autor:
Nahla Hmidi, Dorsaf Makhlouf, Rachida Laamiri, Nahla Kechiche, Badii Hmida, Amine Ksia, Lasaad Sahnoun, Mongi Mekki, Mohsen Belguith, Abdellatif Nouri
Publikováno v:
Iranian Journal of Pediatric Surgery, Vol 6, Iss 1, Pp 50-53 (2020)
Splenogonadal fusion, which is adherence of splenic tissue to gonads, is an uncommon congenital anomaly which mainly affects males. Herein, we report a case of splenogonadal fusion in a 20-month-old boy presenting with acute scrotal pain and inflamma
Externí odkaz:
https://doaj.org/article/ae7b4c6ab2794d7e848ab43fcdaa623c
Autor:
Samia Belhassen, ziza Elezzi, Saida Hidouri, Rachida Laamiri, Sana Mosbahi, Amine Ksiaa, Lassad Sahnoun, Mongi Mekki, Mohsen Belguith, Abdellatif Nouri
Publikováno v:
The Pan African Medical Journal, Vol 38, Iss 345 (2021)
L´urétérocèle est une dilatation pseudo-kystique de l´uretère terminal sous muqueux. C´est une uropathie malformative rare surtout si elle survient sur un uretère simplex. Il s´agit d´une étude rétrospective menée sur dix ans, de 12 doss
Externí odkaz:
https://doaj.org/article/e48951054ad14e49955ad61fda24337b
Autor:
Rachida Laamiri, Nahla Kechiche, Nahla Hmidi, Lassaad Sahnoun, Mongi Mekki, Mohsen Belghith, Amine Ksia, Abdellatif Nouri
Publikováno v:
African Journal of Paediatric Surgery, Vol 18, Iss 2, Pp 117-118 (2021)
Sternal cleft is a rare congenital anomaly which is generally observed at birth. The aetiology remains obscure. Superior clefts are more frequent than inferior ones, and isolated central clefts are extremely rare. Surgery is recommended to protect th
Externí odkaz:
https://doaj.org/article/21a168aca07346cd81a7a4d31041d50e
Autor:
Nahla Kechiche, Dorsaf Makhlouf, Rachida Laamiri, Arije Zouaoui, Salma Mani, Amine Ksiaa, Lasaad Sahnoun, Mongi Mekki, Mohsen Belguith, Abdellatif Nouri
Publikováno v:
Archives of Iranian Medicine. 25:844-846
Heterotopic pancreas (HP) is a rare congenital developmental anomaly of the gastro-intestinal tract, defined as the presence of pancreatic tissue found in ectopic sites. Intussusception caused by isolated HP is extremely rare. Pediatric reports conce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44906f7d7d34dff9ffc132c655505792
https://doi.org/10.34172/aim.2022.131
https://doi.org/10.34172/aim.2022.131
Autor:
Samia Belhassen, Nahla Kechiche, Rachida Laamiri, Imed Krichen, Sana Mosbahi, Amine Ksiaa, Mongi Mekki, Nouri Abdellatif
Publikováno v:
Iranian Journal of Pediatric Surgery, Vol 2, Iss 2, Pp 96-100 (2017)
Introduction: The rectum villous tumour is an uncommon pathology in paediatrics, it represents 1% of all the children’s malignant tumours. Case Presentation: An eleven-year-old girl presented a rectal adenocarcinoma arising from a villous tumour.
Externí odkaz:
https://doaj.org/article/fc2615143c25400991d5579f16cd565e
Autor:
Samia Belhassen, Lassaad Sahnoun, Saloua Ammar, Amine Ksiaa, Rachida Laamiri, Mongi Mekki, Imed Krichene, Mohsen Belghith, Nouri Abdellatif
Publikováno v:
Iranian Journal of Pediatric Surgery, Vol 2, Iss 1, Pp 16-20 (2016)
Introduction: Double aortic arch (DAA) is a rare congenital malformation. Strategies for diagnosis and treatment are different. Reports of thoracoscopic treatment of DAA are rare. We report a description of our diagnostic and therapeutic approach and
Externí odkaz:
https://doaj.org/article/46bde0b602c34973b6f63da66e68725c
Autor:
Rachida Laamiri, Nahla Kechiche, Meriem Braiki, Rim Hadhri, Lassaad Sahnoun, Mongi Mekki, Mohsen Belghith, Abdellatif Nouri
Publikováno v:
Journal of Neonatal Surgery, Vol 7, Iss 1 (2018)
Solitary intestinal myofibromatosis (SIF) is a very rare condition affecting the pediatric population and carries good prognosis following adequate management based on segmental resection. We describe a rare case who presented with features of neonat
Externí odkaz:
https://doaj.org/article/bbf6495da403486e83028c54e50d98b0
Autor:
Rachida Laamiri, Amine Fredj Daassa, Amina Chaka, Kamel Ktari, Abdellatif Nouri, Wadye Hamdouni
Publikováno v:
African Journal of Urology, Vol 27, Iss 1, Pp 1-7 (2021)
Background Testicular microlithiasis in children was defined for the first time in 1961 based on histological criteria. There should be more than 5 calcifications per testicle in order to say that the patient has testicular microlithiasis. It has thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89b87cd78a8de5c0971e3541866dac94
https://doaj.org/article/3cec44c6c39c4b3d85b695ead33719b4
https://doaj.org/article/3cec44c6c39c4b3d85b695ead33719b4