Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Nadia Kasdallah"'
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:
Samia Hannachi, Nadia Kasdallah, Ali Saad, H. Bouthour, Lamia BenJemaa, Houweyda Jilani, Dorra H'mida Ben-Brahim, H. Sassi, Molka Sebai, Jasmin Beygo, Imen Rejeb, Syrine Hizem, Yasmina Elaribi, Karin Buiting
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
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 and rarely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d169c88acc49bed58603bab7f8ef258b
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85114661901
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85114661901
Autor:
Sonia Blibech, Lilia Kraoua, Sonia Abdelhak, Laurent Argiro, R. M’rad, Heather C. Etchevers, Hager Jaouadi, Amel Ben Chehida, Nicolas Lévy, Rym Benkhalifa, Neji Tebib, Nadia Kasdallah, Valérie Delague, Stéphane Zaffran
Publikováno v:
Genetics Research
Genetics Research, Cambridge University Press (CUP), 2019, 101, pp.e6. ⟨10.1017/S0016672319000041⟩
Genetics Research, Cambridge University Press (CUP), 2019, 101, pp.e6. ⟨10.1017/S0016672319000041⟩
Noonan syndrome and related disorders are a group of clinically and genetically heterogeneous conditions caused by mutations in genes of the RAS/MAPK pathway. Noonan syndrome causes multiple congenital anomalies, which are frequently accompanied by h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2d59aea2590c5b0e9d9be1cbffd2568
https://doi.org/10.1017/s0016672319000041
https://doi.org/10.1017/s0016672319000041
Autor:
Nadia, Kasdallah, Hatem, Ben Salem, Hakima, Kbaier, Chaker, Bouguerra, Sonia, Blibech, Mohamed, Douagi
Publikováno v:
La Tunisie medicale. 95(2)
As assisted reproductive therapies (ART) become more common in Tunisia, it was relevant to define the associated perinatal risks. The risk of multiple births and its correlate after ART were well admitted. We aimed to disclose whether ART were associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2cb86343d342bdc573c98c326f04a881
https://pubmed.ncbi.nlm.nih.gov/29424868
https://pubmed.ncbi.nlm.nih.gov/29424868
Publikováno v:
La Tunisie medicale. 95(2)
Congenital diaphragm eventration is a rare and usually asymptomatic developmental defect. Neonatal gastric perforation is also a rare but lifethreatening condition. In our knowledge, the association of these two pathologies has been, exceptionally re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d96f79263679e63cb82d136393a4dcb2
https://pubmed.ncbi.nlm.nih.gov/29424874
https://pubmed.ncbi.nlm.nih.gov/29424874
Autor:
Nadia, Kasdallah, Hatem, Ben Salem, Hakima, Kbaier, Monia, Ouederni, Sonia, Blibech, Mohamed, Douagi
Publikováno v:
La Tunisie medicale. 95(1)
Inherited ADMATS13 or Upshaw-Schulman syndrome (USS) is caused by the deficiency of the Von Willebrand factor-cleaving protease. It is characterized by recurrent episodes of thrombocytopenia reversible by fresh frozen plasma (FFP) infusions, microang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f17426b7a28529698d2127f1b64a5fcf
https://pubmed.ncbi.nlm.nih.gov/29327771
https://pubmed.ncbi.nlm.nih.gov/29327771
Autor:
Nadia, Kasdallah, Hakima, Kbaier, Hatem, Ben Salem, Sonia, Blibech, Asma, Bouziri, Mohamed, Douagi
Publikováno v:
La Tunisie medicale. 94(12)
Povidone iodine (PVI) pleurodesis is commonly used in adult. However, this procedure is still nonconsensual in newborns.This article aimed to report a new case of refractory congenital chylothorax (CCT) managed with PVI pleurodesis with a review of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::75f29656a63c292992f1b3d697029992
https://pubmed.ncbi.nlm.nih.gov/28994881
https://pubmed.ncbi.nlm.nih.gov/28994881