Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Habib Bouthour"'
Autor:
Malak Boughdir, Aida Daib, Habib Bouthour, Sameh Tlili, Syrine Laribi, Rym Kchaou, Rabiaa Ben abdallah, Youssef Hellal, Nejib Kaabar
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 76, Iss , Pp 102115- (2022)
Congenital bronchopulmonary foregut malformation (CBPFM) is a rare congenital malformation involving both the digestive and the respiratory system. Esophageal lung is an entity belonging to this group. Few cases have been reported. Diagnostic can be
Externí odkaz:
https://doaj.org/article/08ef54f4908a4c11bcfe17c2c2d51d25
Autor:
Hela Sassi, Yasmina Elaribi, Houweyda Jilani, Imen Rejeb, Syrine Hizem, Molka Sebai, Nadia Kasdallah, Habib Bouthour, Samia Hannachi, Jasmin Beygo, Ali Saad, Karin Buiting, Dorra H’mida Ben‐Brahim, Lamia BenJemaa
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract Background Beckwith–Wiedemann syndrome (BWS) is a rare overgrowth syndrome characterized by congenital malformations and predisposition to embryonic tumors. Loss of methylation of imprinting center 2 (IC2) is the most frequent alteration a
Externí odkaz:
https://doaj.org/article/fc40ee2cb6c545c19d90a77e319e55ec
Autor:
Mohamed Zouari, Habib Bouthour, Rabia Ben Abdallah, Youssef Hlel, Riath Ben Malek, Youssef Gharbi, Kaabar Nejib
Publikováno v:
African Journal of Paediatric Surgery, Vol 11, Iss 4, Pp 330-333 (2014)
Background: Alimentary tract duplications (ATDs) are a rare condition in children, characterised by a large pathogenic, clinical, and histological polymorphism. Surgical observation and pathologic evaluation of the resected specimens are the only way
Externí odkaz:
https://doaj.org/article/06465a21e51c440c9b93dd4fb4a04917
Autor:
Mohamed Zouari, Houda Kamoun, Habib Bouthour, Rabia Ben Abdallah, Youssef Hlel, Riath Ben Malek, Youssef Gharbi, Nejib Kaabar
Publikováno v:
African Journal of Paediatric Surgery, Vol 11, Iss 1, Pp 22-25 (2014)
Background: Peptic oesophageal stricture (PES) is a serious complication of gastroesophageal reflux disease (GERD) in childhood. The treatment of PES is still controversial, ranging from simple oesophageal dilations to resection/anastomosis of the st
Externí odkaz:
https://doaj.org/article/22095ea50b6845c1adc066d5e755f673
Autor:
Asma Jabloun, Habib Bouthour, Samer Bustame, Fatma Trabelsi, Rabiaa Ben Abdallah, Najib Kaabar
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 13, Iss C, Pp 6-7 (2016)
The presence of a vermiform appendix in an inguinal hernia sac is known as Amyand's hernia. It is an uncommon and rare condition estimated to be found in approximately 1 % of hernia. However, in just 0.08 %, the condition is complicated by an acute a
Externí odkaz:
https://doaj.org/article/83d0fbad90254ec8ab31654af8ab75e0
Autor:
Mohamed, Zouari1 zouarimohamed.1982@yahoo.fr, Habib, Bouthour1, Abdallah Rabia, Ben1, Youssef, Hlel1, Malek Riath, Ben1, Youssef, Gharbi1, Nejib, Kaabar1
Publikováno v:
African Journal of Paediatric Surgery. Jan-Mar2014, Vol. 11 Issue 1, p79-81. 3p. 2 Black and White Photographs.
Autor:
Néjib, Kaabar, Rabiaa, Ben Abdallah, Houssem, Yengui, Youssef, Hellal, Riadh, Ben Malek, Habib, Bouthour, Sadok, Sayed
Publikováno v:
La Tunisie medicale. 92(4)
Wandering spleen is a rare entity in child. It is generated by laxity or failure of development of spleen ligaments causing the migration of the spleen from its normal anatomical site to another abdominal or pelvic location. It can be congenital or a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ee5362edee50cd66f0e1f8123423b81
https://pubmed.ncbi.nlm.nih.gov/25224425
https://pubmed.ncbi.nlm.nih.gov/25224425
Autor:
Rabiaa, Ben Abdallah, Habib, Bouthour, Youssef, Hellal, Mohamed Riadh, Ben Malek, Youssef, Gharbi, Nejib, Kaabar
Publikováno v:
La Tunisie medicale. 91(1)
Congenital broncho-pulmonary malformations (CBM) are rare, essentially presented by congenital lobar emphysema, bronchogenic cysts, pulmonary sequestrations and cystic adenomatoid malformations. The diagnosis can be in prenatal. In postnatal, symptom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::afe32495f4283d43ed0eaf52904b1463
https://pubmed.ncbi.nlm.nih.gov/23404602
https://pubmed.ncbi.nlm.nih.gov/23404602
Autor:
Nejib, Kaabar, Habib, Bouthour, Rabiaa, Ben Abdallah, Salma, Hachicha, Youssef, Hellal, Riadh, Ben Malek, Mongi, Ben Hriz, Sadok, Sayed
Publikováno v:
La Tunisie medicale. 89(2)
Duodenum duplications are uncommon congenital anomalies. Most symptomatic cases are diagnosed in childhood and usually present with obstructive or bleeding symptoms. Acute pancreatitis is rarely attributed to these cysts.To report a new case of duode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73e652f040bff9b48c8e109c64cf8d88
https://pubmed.ncbi.nlm.nih.gov/21308632
https://pubmed.ncbi.nlm.nih.gov/21308632
Autor:
Y. Hlel, Kaabar Nejib, Y. Gharbi, Mohamed Zouari, Habib Bouthour, Rabia Ben Abdallah, Riath Ben Malek
Publikováno v:
African Journal of Paediatric Surgery, Vol 11, Iss 4, Pp 330-333 (2014)
Background: Alimentary tract duplications (ATDs) are a rare condition in children, characterised by a large pathogenic, clinical, and histological polymorphism. Surgical observation and pathologic evaluation of the resected specimens are the only way
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8837c2062f78d9a60a7a86a2b7d2559f
https://doi.org/10.4103/0189-6725.143146
https://doi.org/10.4103/0189-6725.143146