Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marwa Sayeb"'
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hajer Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, CRYSTEL Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/d1f20ca9f1e041b5805610de30e16616
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily due to limited access to com
Externí odkaz:
https://doaj.org/article/d53f3da42b5b4e8f9503ec02796dd375
Autor:
Abir Ben Haj Ali, Ahlem Amouri, Marwa Sayeb, Saloua Makni, Wajih Hammami, Chokri Naouali, Hamza Dallali, Lilia Romdhane, Anu Bashamboo, Kenneth McElreavey, Sonia Abdelhak, Olfa Messaoud
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background Several studies have shown a high rate of consanguinity and endogamy in North African populations. As a result, the frequency of autosomal recessive diseases is relatively high in the region with the co‐occurrence of two or more
Externí odkaz:
https://doaj.org/article/ba14324bf6dd468b87e9e7ef456fff63
Autor:
Sonia Abdelhak, Zied Riahi, Houda Yacoub-Youssef, Nacer Ghilane, Mourad Mokni, Crystel Bonnet, Anissa Zaouak, J. Marrakchi, Christine Petit, Nadia Laroussi, Lilia Romdhane, Oussema Bouchniba, Marwa Sayeb, Olfa Messaoud, Ghaith Abdessalem, Rahma Mkaouar, Ghazi Besbes
Publikováno v:
International Journal of Dermatology. 58:1439-1443
Background Co-occurrence of two genetic diseases is challenging for accurate diagnosis and genetic counseling. The recent availability of whole exome sequencing (WES) has dramatically improved the molecular diagnosis of rare genetic diseases in parti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b85369b67248a8ba861797aa22b4fb5
https://doi.org/10.1111/ijd.14452
https://doi.org/10.1111/ijd.14452
Autor:
Faouzi Maazoul, Wided Kelmemi, S. Echebbi, Ridha Mrad, Nadia Ben Ali, Lilia Kraoua, Marwa Daghsni, Mohamed Kacem Ben Fradj, Saida Lahbib, Sonia Abdelhak, Mariem Kchaou, Marwa Sayeb
Publikováno v:
Cytogenetic and Genome Research. 154:1-5
Juvenile myoclonic epilepsy (JME) is characterized by seizures, severe cognitive abnormalities, and behavior impairments. These features could evolve over time and get worse, especially when the encephalopathy is pharmacoresistant. Thus, genetic stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f78e7553d0bb18a5346c9a6decc82edc
https://doi.org/10.1159/000486945
https://doi.org/10.1159/000486945
Autor:
Marwa, Sayeb, Zied, Riahi, Nadia, Laroussi, Crystel, Bonnet, Lilia, Romdhane, Rahma, Mkaouar, Anissa, Zaouak, Jihene, Marrakchi, Ghaith, Abdessalem, Olfa, Messaoud, Oussema, Bouchniba, Nacer, Ghilane, Mourad, Mokni, Ghazi, Besbes, Houda, Yacoub-Youssef, Christine, Petit, Sonia, Abdelhak
Publikováno v:
International Journal of Dermatology
International Journal of Dermatology, Wiley-Blackwell, 2019, 58 (12), pp.1439-1443. ⟨10.1111/ijd.14452⟩
International Journal of Dermatology, 2019, 58 (12), pp.1439-1443. ⟨10.1111/ijd.14452⟩
International Journal of Dermatology, Wiley-Blackwell, 2019, 58 (12), pp.1439-1443. ⟨10.1111/ijd.14452⟩
International Journal of Dermatology, 2019, 58 (12), pp.1439-1443. ⟨10.1111/ijd.14452⟩
International audience; Background: Co-occurrence of two genetic diseases is challenging for accurate diagnosis and genetic counseling. The recent availability of whole exome sequencing (WES) has dramatically improved the molecular diagnosis of rare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3125ce1e9d247b7e4b0c8558244835e3
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219630
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219630
Autor:
Marwa, Daghsni, Saida, Lahbib, Mohamed, Fradj, Marwa, Sayeb, Wided, Kelmemi, Lilia, Kraoua, Mariem, Kchaou, Faouzi, Maazoul, Slim, Echebbi, Nadia, Ben Ali, Sonia, Abdelhak, Ridha, M'rad
Publikováno v:
Cytogenetic and genome research. 154(1)
Juvenile myoclonic epilepsy (JME) is characterized by seizures, severe cognitive abnormalities, and behavior impairments. These features could evolve over time and get worse, especially when the encephalopathy is pharmacoresistant. Thus, genetic stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0c2f76e2f143b5f3cd7bf4c28eed6a3e
https://pubmed.ncbi.nlm.nih.gov/29490292
https://pubmed.ncbi.nlm.nih.gov/29490292