Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Samia, Younes"'
Autor:
HAMMOUDA, Souha, GHZAIEL, Imen, KHAMLAOUI, Wided, HAMMAMI, Sonia, MHENNI, Samia YOUNES, SAMET, Slim, HAMMAMI, Mohamed, ZARROUK, Amira
Publikováno v:
In Prostaglandins, Leukotrienes and Essential Fatty Acids September 2020 160
Autor:
Samira Younes, Sabria Khouadja, Samia Younes, Rim Ben Soussia, Walid Bouali, Ahmed Haj Mohamed, Lazhar Zarrouk
Publikováno v:
The Pan African Medical Journal, Vol 33, Iss 80 (2019)
Neurofibromatosis type 2 (NF2) is a rare autosomal dominant disorder characterized by formation of central nervous system tumors. They are associated to significant morbidity due to multiple problems such as hearing loss that can lead to many psychia
Externí odkaz:
https://doaj.org/article/87772e3eecef43fcb060df2c23ffb331
Publikováno v:
The Pan African Medical Journal, Vol 33, Iss 117 (2019)
Catatonia occurring as part of a clinical picture of dementia has been reported with almost all types of dementia. It remains under-diagnosed in older adults and those with dementia. We review a case of a young patient admitted in our psychiatric dep
Externí odkaz:
https://doaj.org/article/495866ed4764446ebb0a198b19503fc6
Autor:
Khadija Mansour, Zohra Chadli, Ichrak Ghachem, Nadia Ben Fredj, Haifa Ben Romdhane, Najah Ben Fadhel, Naceurs Boughatas, Karim Aouam, Amel Chaabane, Samia Younes
Publikováno v:
European Journal of Clinical Pharmacology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9d7622f077afceeaa89145ef05d8450
https://doi.org/10.1007/s00228-023-03510-7
https://doi.org/10.1007/s00228-023-03510-7
Autor:
Narjes Mokni, Amel Benammar Elgaaied, Itziar de Rojas, Afef Hammami, Nizar Daouassi, Lotfi Cherni, Agustín Ruiz, Sonia Moreno-Grau, Laura Montrreal, Samia Younes, Imene Mahmoud, Mahbouba Frih-Ayed, Nesrine Ben Salem, Sami Boussetta
Publikováno v:
Molecular Biology Reports. 49:1687-1700
Background Alzheimer's disease (AD) is the most common neurodegenerative disorder in humans and presents a major health problem throughout the world. The etiology of AD is complex, and many factors are implicated, including mitochondria. Mitochondria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba4201a2c54531166c7acd35898143a1
https://doi.org/10.1007/s11033-021-06978-7
https://doi.org/10.1007/s11033-021-06978-7
Autor:
Yosra Cherif, Samia Younes, Olfa Berriche, Baha Zantour, Mahbouba Frih-Ayed, Mohamed Habib Sfar
Publikováno v:
Current Innovations in Medicine and Medical Science Vol. 9 ISBN: 9789355479679
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::effe2438812655fa36a273a50a6d5e25
https://doi.org/10.9734/bpi/cimms/v9/4363e
https://doi.org/10.9734/bpi/cimms/v9/4363e
Autor:
Mouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, Nadia Charfi, Nozha Kallel, Nabila Rekik, Basma Ben Naceur, Hela Fourati, Emna Daoud, Zainab Mnif, Mohamed Habib Sfar, Samia Younes-Mhenni, Mohamed Tahar Sfar, Mongia Hachicha, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 1, Pp 121-127 (2013)
Background: Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis. The enzymes most commonly affected are 21-hydroxylase. Past reports suggested brain magnetic resonance imaging (MRI) abnormalities in CAH
Externí odkaz:
https://doaj.org/article/3fa499640002449e8efeaed951b32800
Autor:
Nesrine Ben Salem, Sami Boussetta, Itziar de Rojas, Sonia Moreno-Grau, Laura Montrreal, Narjes Mokni, Imene Mahmoud, samia Younes, Nizar Daouassi, Mahbouba Frih-Ayed, Afef Hammami, Amel Ben Ammar Elgaaied, Agustín Ruiz, Lotfi Cherni
Publikováno v:
Molecular biology reports. 49(3)
Background: Alzheimer’s disease (AD) is the most common neurodegenerative disorder in humans and presents a major health problem throughout the world. The etiology of AD is complex, and many factors are implicated, including mitochondria. Mitochond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d589e2fa1f0dfafdbbf1f6811acb59e
https://pubmed.ncbi.nlm.nih.gov/34854014
https://pubmed.ncbi.nlm.nih.gov/34854014
Publikováno v:
The Pan African Medical Journal, Vol 21, Iss 141 (2015)
La granulomatose avec polyangéite (GPA) est une vascularite nécrosante systémique, caractérisée par une inflammation granulomateuse, une nécrose tissulaire et une vascularite touchant les vaisseaux de moyen et, surtout, de petit calibre, elle t
Externí odkaz:
https://doaj.org/article/b7f17d98199e4b49a1ab3da349094193