Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Lamia Boughamoura"'
Autor:
Ines Brini, Aida Guerrero, Naila Hannachi, Jihene Bouguila, Dorothea Orth-Höller, Amira Bouhlel, Lamia Boughamoura, Benjamin Hetzer, Wegene Borena, Britta Schiela, Dorothee Von Laer, Jalel Boukadida, Heribert Stoiber
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0188325 (2017)
This study aimed to identify a broad spectrum of respiratory pathogens from hospitalized and not-preselected children with acute respiratory tract infections in the Farhat Hached University-hospital of Sousse, Tunisia. Between September 2013 and Dece
Externí odkaz:
https://doaj.org/article/d6024f26f71444b6986032240960294b
Autor:
Maher Jedidi, Samia Tilouche, Tasnim Masmoudi, Maha Sahnoun, Youssef Chkirbène, Sarra Mestiri, Lamia Boughamoura, Mohamed Ben Dhiab, Mohamed Kamel Souguir
Publikováno v:
Autopsy and Case Reports, Vol 6, Iss 4 (2016)
Myocarditis is an inflammatory disease of the myocardium with heterogeneous clinical manifestations and progression. In clinical practice, although there are many methods of diagnosis of acute myocarditis, the diagnosis remains an embarrassing dilemm
Externí odkaz:
https://doaj.org/article/608d9fecf6354b2c8665bafa1120969a
Autor:
Leila Essaddam, Ons Zitouni, Lilia Kraoua, Madiha Trabelsi, Hella Sassi, Sana Kmiha, Fatma Charfi, Dorra El Guiche, Raoudha Kebaïli, Nesrine Jaballah, Maroua Rjeb, Noura Zouari, Yasmina El Aribi, Syrine Hizem, Salmen Wannes, Ibtihel Fkih Romdhane, Mohamed Tahar Sfar, Hechmi Ben Hamouda, Radhia Hadj Salem, Zied Khlayfia, Tarek Khmiss, Kamel Monastiri, Nadia Siala, Slaheddine Chouchane, Habib Souaa, Inès Khochtali, Bahri Mahjoub, Habib Sfar, Lamia Ben Jemâa, Saoussen Abroug, Lamia Boughamoura, Inès Kamoun, Thouraya Kamoun, Ridha Mrad, Saayda Ben Becher
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism.
Objectives Early diagnosis in Turner syndrome is desirable to optimize growth and puberty and yet, it is often made late. Here, we aim to identify age at diagnosis, clinical features at presentation and potential strategies to improve the care of TS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b15567b24b1ac497acfb79bc72641173
https://doi.org/10.1515/jpem-2022-0360
https://doi.org/10.1515/jpem-2022-0360
Autor:
Jihene Bouguila, Zahra Malekshahi, Ines Brini, Jalel Boukadida, Dorothea Orth-Höller, Imene Handous, Sonia Nouri-Merchaoui, Heribert Stoiber, Lamia Boughamoura, Reinhard Würzner, Dorothee von‐Laer, Nabiha Mahdhaoui, Naila Hannachi, Benjamin Hetzer, Olfa Hazgui, Issaad‐Kawther Ezzine, Aida Guerrero
Publikováno v:
Journal of Medical Virology
Background The human Adenovirus (HAdV) is a common agent of acute respiratory infections (ARIs). Its clinical impact in immunocompetent children and in the context of coinfections remains unclear in Tunisia. Material and methods HAdV‐ARIs were stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b004e9bd23e78dd4882eb0ac312ce72
https://doi.org/10.1002/jmv.26375
https://doi.org/10.1002/jmv.26375
Autor:
Sondess Hadj Fredj, Sihem Barsaoui, Lamia Boughamoura, Taieb Messaoud, Ahmed Mehrezi, Sonia Hilioui, Jihene Bouguila, S. Hamouda, Salma Ben Ameur, Khadija Boussetta, H. Ajmi, Mohamed Taher Sfar, N. Mattoussi, Saida Ben Becheur, Saoussen Abroug, Neji Tebib, Habib Besbes, Raoudha Boussoffara, F. Khalsi, Najoua Gandoura, N. Gueddiche, Faten Tinsa, A. Samoud, Mongia Hachicha
Publikováno v:
African Health Sciences
Aim: To establish a preliminary national report on clinical and genetic features of cystic fibrosis (CF) in Tunisian children as a first measure for a better health care organization. Methods: All children with CF diagnosed by positive sweat tests be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58daacc0a9a93c7fc15a5a5729e83529
https://pubmed.ncbi.nlm.nih.gov/33402933
https://pubmed.ncbi.nlm.nih.gov/33402933
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a57bb5c13e4bc33cd021074e4a01e950
https://doi.org/10.1530/endoabs.70.ep567
https://doi.org/10.1530/endoabs.70.ep567
Autor:
Sana Bhiri, Sonia Nouri Merchaoui, Jihene Bougila, Lamia Boughamoura, Nabiha Mahdhaoui, Naila Hannachi, Dorothea Orth-Höller, Hassen Sboui, Aida Guerrero, Ines Brini Khalifa, Jalel Boukadida, Heribert Stoiber, Dorothee von Laer, Britta Schiela
Publikováno v:
Journal of Medical Virology
Background This study aimed to characterize the epidemiology of pathogenic respiratory agents in patients aged 0 to 12 months and hospitalized for acute respiratory infections in Tunisia between 2013 and 2014. Methods A total of 20 pathogens, includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af5776b55645809260ea9c58c8055132
https://doi.org/10.1002/jmv.25347
https://doi.org/10.1002/jmv.25347
Autor:
Imed Mabrouk, Rahma Mani, Jihen Bouguila, Lamia Boughamoura, Mongia Hachicha, Raoudha Boussoffara, Salma Ben Ameur, Samia Hammouda, Khadija Boussetta, Zohra Soua
Publikováno v:
International Journal of Medical Research and Health Sciences, Vol 7, Iss 9, Pp 120-126 (2018)
Background: PCR-coupled single-strand conformation polymorphism (PCR-SSCP) is often used as a first line screening technique to facilitate mutation detection in large genes such as the DNAH5 gene. A modified protocol of PCR-SSCP by primers addition b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::5100940ad73c29274d5e11dc4a1468eb
https://www.ijmrhs.com/medical-research/improved-sscp-analysis-through-primers-addition-to-screen-hotspot-exons-in-dnah5-gene.pdf
https://www.ijmrhs.com/medical-research/improved-sscp-analysis-through-primers-addition-to-screen-hotspot-exons-in-dnah5-gene.pdf
Autor:
Faiza Fakhfakh, Emna Mkaouar-Rebai, Leila Keskes, Marwa Ammar, Amel Tej, Rahma Felhi, Jihene Bouguila, Senda Majdoub, Mouna Tabbebi, Samia Tilouche, Marwa Maalej, Boudour Khabou, Lamia Boughamoura
Publikováno v:
Biochemical and Biophysical Research Communications. 495:1730-1737
Deficiency of the mitochondrial enzyme succinyl COA ligase (SUCL) is associated with encephalomyopathic mtDNA depletion syndrome and methylmalonic aciduria. This disorder is caused by mutations in both SUCL subunits genes: SUCLG1 (α subnit) and SUCL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::064427522b0e0ac37f7a3d3bb28469bf
https://doi.org/10.1016/j.bbrc.2017.12.011
https://doi.org/10.1016/j.bbrc.2017.12.011
Autor:
Hajer Ben Belgacem, Lamia Boughamoura, Raoudha Kebaili, Samia Ben Hassan, Koussay Eleuch, Abdelatif Nouri, Sana Alilech, Amel Tej, Yosra Hasni
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab867bb0e4b9ee85b90950058453549a
https://doi.org/10.1530/endoabs.63.p459
https://doi.org/10.1530/endoabs.63.p459