Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Jihene, Marrakchi"'
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:
Anis Grassa, Meriem Yazidi, Jihene Marrakchi, Chaima Bel Hadj Sliman, Ibtissem Oueslati, Melika Chihaoui
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Pallister–Hall syndrome (PHS) is a very rare genetic disorder. The diagnosis is usually suspected at the young age when a hypothalamic hamartoma is associated with polydactyly. Endocrine manifestations are mostly related to hypothalamic ha
Externí odkaz:
https://doaj.org/article/538ea47061d6486fa829e22a04172fd1
Autor:
Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, Imen Chelly, Hela Boudabbous, Hamza Dallali, Crystel Bonnet, Meriem Hechmi, Soumeya Bekri, Nadia Zitouna, Lotfi Zekri, Amel Tounsi, Rym Kefi, Jihene Marrakchi, Olfa Messaoud, Ichraf Kraoua, Sonia Maalej, Ilhem Turki Ben Youssef, Ahlem Ben Hmid, Fabrice Giraudet, Sami Bouchoucha, Neji Tebib, Ghazi Besbes, Christine Petit, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0258202 (2021)
Alpha-Mannosidosis (AM) is an ultra-rare storage disorder caused by a deficiency of lysosomal alpha-mannosidase encoded by the MAN2B1 gene. Clinical presentation of AM includes mental retardation, recurrent infections, hearing loss, dysmorphic featur
Externí odkaz:
https://doaj.org/article/569f864a04af411d83938661f5680131
Autor:
Zouhair Mbarki, Jihene Marrakchi, Seif Boukriba, Salam Labidi, Amine Ben Slama, Hassen Seddik
Publikováno v:
Traitement du Signal. 38:955-965
Manual assessment of parotid gland status from magnetic resonance imaging is a subjective, time consuming and error prone process. Automatic image analysis methods offer the possibility to get consistent, objective and rapid diagnoses of parotid glan
Autor:
Houda Chahed, Ghada Kharra, Rim Bechraoui, Jihene Marrakchi, zza Mediouni, Mohamed Ben Amor, Rim Zainine, Nejeh Beltaief, Ghazi Besbes
Publikováno v:
The Pan African Medical Journal, Vol 27, Iss 43 (2017)
Ectopic thyroid tissue (ETT) lateral to the midline is rare. Its occurrence in the carotid bifurcation is exceptional. We present a 45 years woman who consulted with a slow growing right cervical swelling. Clinical examination Ultrasonography, contra
Externí odkaz:
https://doaj.org/article/e8229a4896ac4c6eb0b5ed3ecd9e31bf
Autor:
Ibtissem Oueslati, Hiba-Allah Chatti, Aymen Azaiez, Jihene Marrakchi, Seif Boukriba, Slim Haouet, Meriem Yazidi, Melika Chihaoui
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Computer Methods in Biomechanics and Biomedical Engineering. 24:400-418
Vertigo is a common sign related to a problem with the brain or vestibular system. Detection of ocular nystagmus can be a support indicator to distinguish different vestibular disorders. In order to get reliable and accurate real time measurements fr
Hybrid clustering system using Nystagmus parameters discrimination for vestibular disorder diagnosis
Autor:
Hedi Trabelsi, Jihene Marrakchi, Aymen Mouelhi, Hanene Sahli, Seif Boukriba, Amine Ben Slama, Mounir Sayadi
Publikováno v:
Journal of X-Ray Science and Technology. 28:923-938
BACKGROUD AND OBJECTIVE: The control of clinical manifestation of vestibular system relies on an optimal diagnosis. This study aims to develop and test a new automated diagnostic scheme for vestibular disorder recognition. METHODS: In this study we s
Publikováno v:
Computer Methods in Biomechanics and Biomedical Engineering: Imaging & Visualization. 8:681-690
The Vestibulo-ocular response VOR is characterized by a smooth pursuit eye movements in one direction, called slow phase of ocular nystagmus, interrupted by resetting saccades fast phase of nystagm...