Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Faten Tinsa"'
Autor:
Khadija Boussetta, Ines Brini, Manel Ben Romdhane, Faten Tinsa, Neji Tebib, Soumeya Bekri, Imen Bel Hadj, Hela Louati, Hela Boudabous
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:e193-e196
Wolman disease is an ultrarare lysosomal storage disease caused by a mutation in the LIPA gene. The clinical features of Wolman disease include early onset of vomiting, diarrhea, failure to thrive, hepatosplenomegaly, and bilateral adrenal calcificat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d94c8d70907becb5d144dd23780a696
https://doi.org/10.1097/mph.0000000000001192
https://doi.org/10.1097/mph.0000000000001192
Autor:
Imen, Bel Hadj, Inès, Trabelsi, Faten, Tinsa, Manel, Ben Romdhane, Nada, Fersi, Fatma, Khalsi, Khadija, Boussetta
Publikováno v:
La Tunisie Médicale
Background: Acute bronchiolitis management involves all pediatricians and primary care physicians. The national guidelines for bronchiolitis diagnosis and treatment were published in Tunisia to reduce excessive use of diagnostic tests and unify bronc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7df2e1b34be5caf189daa67223fca696
https://pubmed.ncbi.nlm.nih.gov/33899193
https://pubmed.ncbi.nlm.nih.gov/33899193
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:
African Health Sciences
African Health Sciences; Vol 18, No 3 (2018); 539-541
African Health Sciences; Vol 18, No 3 (2018); 539-541
Rabies is a ubiquitous fatal disease and its large wild life reservoir may precipitate a flare-up whenever stringent control is relaxed. It remains a serious public health challenge in the developing world. It is estimated that up to 40–60,000 case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db208ae299426ee47aad42d855c2d3ab
http://europepmc.org/articles/PMC6307015
http://europepmc.org/articles/PMC6307015
Autor:
Imen, Bel Hadj, Riadh, Boukhris, Fatma, Khalsi, Manel, Namouchi, Iheb, Bougmiza, Faten, Tinsa, Samia, Hamouda, Khadija, Boussetta
Publikováno v:
La Tunisie medicale. 97(3)
Due to the marked decline of maternal-fetal rhesus incompatibility, ABO alloimmunization has become the leading cause of the newborn hemolytic disease. It is estimated that 15-25 % of all pregnancies are concerned by ABO incompatibility.Neonatal bloo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54c29d3bc5f7517f7c65595c21913e3e
https://pubmed.ncbi.nlm.nih.gov/31729720
https://pubmed.ncbi.nlm.nih.gov/31729720
Autor:
Rym Kefi, Imen Bel Hadj, Sonia Abdelhak, F. Khalsi, M. Hechmi, H. Azouz, K. Boussetta, Mariem Chargui, Faten Tinsa
Publikováno v:
Revue Neurologique
Revue Neurologique, Elsevier Masson, 2019, 175 (5), pp.324-327. ⟨10.1016/j.neurol.2018.07.008⟩
Revue Neurologique, Elsevier Masson, 2019, 175 (5), pp.324-327. ⟨10.1016/j.neurol.2018.07.008⟩
International audience; Letter to the Editor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0acac08ae1f079e20e2257ad3dced36
https://hal-riip.archives-ouvertes.fr/pasteur-01999932
https://hal-riip.archives-ouvertes.fr/pasteur-01999932
Autor:
Faten, Tinsa, Hajer, Barakizou, Imen, Belhadj, Zohra, Fitouri, Aida, Borgi, Azza, Samoud, Saida, Ben Becher, Najla, Ben Jabbalah, Olfa, Bouyahia, Khadija, Boussetta
Publikováno v:
La Tunisie medicale. 96(6)
Influenza A (H1N1) is a contagious acute respiratory infection caused a pandemic in 2009. The outcome was variable among populations.To describe a clinical spectrum and the outcome of Tunisian children with pandemic H1N1/09 influenza virus.This is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2bf8e66263f11396eebac8ecb6f9d5c5
https://pubmed.ncbi.nlm.nih.gov/30430472
https://pubmed.ncbi.nlm.nih.gov/30430472
Autor:
Ines Trabelsi, Faten Tinsa, Manel Ben Romdhane, Imen Belhadj, S. Hamouda, Khadija Boussetta, F. Khalsi
Publikováno v:
Imaging.
Background: Post infectious bronchiolitis obliterans (PIBO) is a serious disease in children. The chest computed tomography (CCT) lesions are varied. The correlation between the severity of clinical symptoms and the importance of radiological signs i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::664c962757c3d60f91127e6b2c76f86b
https://doi.org/10.1183/13993003.congress-2018.pa386
https://doi.org/10.1183/13993003.congress-2018.pa386
Autor:
K. Boussetta, S. Hamouda, I. Bel Hadj, M. Ben Romdhane, Sonia Abdelhak, Faten Tinsa, Hela Louati, F Riant, E. Tournier-Lasserve, I. Brini
Publikováno v:
Revue Neurologique
Revue Neurologique, Elsevier Masson, 2019, 175 (3), pp.194-197. ⟨10.1016/j.neurol.2018.04.013⟩
Revue Neurologique, Elsevier Masson, 2019, 175 (3), pp.194-197. ⟨10.1016/j.neurol.2018.04.013⟩
International audience; Familial CCM is a rare entity associated with the mutation of three genes: CCM1 (KRIT1), CCM2 (MGC4607), and CCM3 (PDCD10). We report here the first description of a Tunisian familial CCMs composed of six members. The father a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc76d2dfb824f806963269239deda4f7
https://pubmed.ncbi.nlm.nih.gov/30314744
https://pubmed.ncbi.nlm.nih.gov/30314744
Autor:
Taieb Messaoud, F. Khalsi, Faten Tinsa, Sondes Hadj Fredj, Sonia Abdelhak, Imen Bel Hadj, Khadija Boussetta
Publikováno v:
Annales de biologie clinique. 75(4)
Pseudo-Bartter syndrome (PBS) describes an uncommon complication of cystic fibrosis leading to hypochloraemic, hypokalaemic metabolic alkalosis. PBS as the sole manifestation of cystic fibrosis in children is extremely rare and has never been describ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31abb4f90ae86f4c6a8f83f7c0f34ec0
https://pubmed.ncbi.nlm.nih.gov/28751295
https://pubmed.ncbi.nlm.nih.gov/28751295