Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Lilia, Kraoua"'
Autor:
Dhekra Ismail, Lilia Kraoua, Sylvie Jaillard, Hela Bellil, Mohamed Zairi, Faouzi Maazoul, Ridha Mrad, Mohamed Nabil Nessib, Mediha Trabelsi
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-9 (2024)
Abstract Background Interstitial chromosome 11 long arm deletions (11q13-q23) represent a rare cytogenetic abnormality characterized by non-specific clinical features including intellectual disability and several malformations without a clear genotyp
Externí odkaz:
https://doaj.org/article/0ce03cf3ee914d5480ebaf5acbd4d46f
Autor:
Ichraf Kraoua, Maha Jamoussi, Cyrine Drissi, Lilia Kraoua, Séverine Drunat, Hanene Benrhouma, Thouraya Ben Younes, Sonia Nagi, Sonia Abdelhak, Odile Boespflug Tanguy, Ilhem Ben Youssef‐Turki, Mediha Trabelsi, Imen Dorboz
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 10, Pp n/a-n/a (2024)
ABSTRACT Background POLIII‐related leukodystrophies are a group of recently recognized hereditary white matter diseases with a similar clinical and radiological phenotype. No Tunisian studies have been published about POLIII‐related leukodystroph
Externí odkaz:
https://doaj.org/article/42e56d894f30444d9f78ebe123d5a36b
Autor:
Lilia Kraoua, Assaad Louati, Sarra Ben Ahmed, Nesrine Abida, Monia Khemiri, Khaled Menif, Ridha Mrad, Stéphane Zaffran, Hager Jaouadi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract Background Dilated cardiomyopathy (DCM) is characterized by dilatation of the left ventricle, systolic dysfunction, and normal or reduced thickness of the left ventricular wall. It is a leading cause of heart failure and cardiac death at a y
Externí odkaz:
https://doaj.org/article/76c100c1d70747fd84a8abf7825d3273
Autor:
Ismail Gouiza, Meriem Hechmi, Abir Zioudi, Hamza Dallali, Nadia Kheriji, Majida Charif, Morgane Le Mao, Said Galai, Lilia Kraoua, Ilhem Ben Youssef-Turki, Ichraf Kraoua, Guy Lenaers, Rym Kefi
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Introduction: Inherited mitochondrial diseases are the most common group of metabolic disorders caused by a defect in oxidative phosphorylation. They are characterized by a wide clinical and genetic spectrum and can manifest at any age. In this study
Externí odkaz:
https://doaj.org/article/d0d0662ffbeb44a0b3f31c44fdd41dc5
Autor:
Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, Ahlem Achour, Hakim Kaouther, Habib Ben Ahmed, Lilia Chaker, Faouzi Maazoul, Fatma Ouarda, Stéphane Zaffran, Ridha M'rad
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract Background Genetic cardiac diseases are the main trigger of sudden cardiac death (SCD) in young adults. Hypertrophic cardiomyopathy (HCM) is the most prevalent cardiomyopathy and accounts for 0.5 to 1% of SCD cases per year. Methods Herein,
Externí odkaz:
https://doaj.org/article/a8ed9491d0fc400688d138cae0ad8928
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::035636127f094a4034051164da66f5ed
https://doi.org/10.1530/endoabs.90.ep924
https://doi.org/10.1530/endoabs.90.ep924
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
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, 2023, 24 (4), ⟨10.3390/ijms24043365⟩
International Journal of Molecular Sciences, 2023, 24 (4), ⟨10.3390/ijms24043365⟩
International audience; Calcium (Ca 2+) is the major mediator of cardiac contractile function. It plays a key role in regulating excitation-contraction coupling and modulating the systolic and diastolic phases. Defective handling of intracellular Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92bea2931cd668a9f65f3a41b7da0b2c
https://hal-amu.archives-ouvertes.fr/hal-04004374/document
https://hal-amu.archives-ouvertes.fr/hal-04004374/document
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebeeb608b8435a73cb4d95a6a3b5e0a0
https://doi.org/10.1530/endoabs.73.aep609
https://doi.org/10.1530/endoabs.73.aep609
Autor:
Mediha Trabelsi, Lilia Kraoua, Ahlem Achour, Cyrine Adhoum, Faouzi Maazoul, Hana Fredj, Ridha Mrad
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02a087f6e4477ae1e93b30d87c744f28
https://doi.org/10.1530/endoabs.73.aep602
https://doi.org/10.1530/endoabs.73.aep602