Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Sana, Chaouki"'
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5863-5866 (2024)
Osteopetrosis, also known as the disease of marbled bones, refers to a group of constitutional bone diseases resulting from a defect in bone metabolism. This condition is characterized by its manifestation, most often at a young age, and is typically
Externí odkaz:
https://doaj.org/article/66a220693ad742f788ca3ef6ead6f7ef
Autor:
Hinde El Mouhi, Meriame Abbassi, Meryem Jalte, Abdelhafid Natiq, Laila Bouguenouch, Sana Chaouki
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 2, Pp 67-82 (2024)
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy, is a severe epileptic syndrome affecting children, with an incidence of 1/22,000 to 1/49,900 live births annually. Characterized by resistant and prolonged seizures, it o
Externí odkaz:
https://doaj.org/article/8bf80ad138e640d29c02084f77c3bf97
Autor:
Mohamed Ahakoud, Hanae Daha Belghiti, Ayoub Nedbour, Abdelhamid Bouramtane, Sana Chaouki, Laila Bouguenouch, Karim Ouldim
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bac2a500472b2efe687e601ac828a399
https://doi.org/10.7759/cureus.37866
https://doi.org/10.7759/cureus.37866
Autor:
Sahar Amrani Hanchi, Hasnae Hoummani, Hajar Mourabiti, Mohammed Chebaibi, Sana Chaouki, Sanae Achour, Ilham Tadmouri, Moustapha Hida
Publikováno v:
E3S Web of Conferences, Vol 319, p 01077 (2021)
Introduction. —The Covid-19 pandemic and the containment situation, has generated enormous risks for children. Indeed, with the closure of schools, children, forced to stay at home, found themselves in permanent contact with dangerous products (dru
Externí odkaz:
https://doaj.org/article/701502e72a8e4a0197a686d6c8e45a81
Autor:
Mohamed Hbibi, Sara Benmil, Safae Rahmouni, Ilhame Tadmouri, Sana Abourazzak, Sana Chaouki, Fatima Zahra Souilmi, Mounia Lakhdar Idrissi, Mostapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 31, Iss 74 (2018)
Le syndrome d'activation macrophagique (SAM) est une atteinte multisystémique, liée à une intense activation du système immunitaire correspondant à une infiltration plus ou moins diffuse des tissus par des macrophages activés. Il associé des s
Externí odkaz:
https://doaj.org/article/b412de57a4a640e4b22eb20561b9b098
Autor:
Hanae Daha Belghiti, Meriame Abbassi, Hanane Sayel, Mohamed Ahakoud, Badr Eddine El Makhzen, Norman Lee, Silvia Russo, Sana Chaouki, Laila Bouguenouch
Publikováno v:
Journal of Pediatric Genetics.
Angelman syndrome (AS) is a rare neurodevelopmental disorder due to genetic defects involving chromosome 15, known by intellectual disability, cognitive and behavioral disorders, ataxia, delayed motor development, and seizures. This study highlights
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8484f172826cd6ad49cf2c8f9e4d9df9
https://doi.org/10.1055/s-0042-1751268
https://doi.org/10.1055/s-0042-1751268
Autor:
Tanuja Chitnis, Brenda Banwell, Ludwig Kappos, Douglas L Arnold, Kivilcim Gücüyener, Kumaran Deiva, Natalia Skripchenko, Li-Ying Cui, Stephane Saubadu, Wenruo Hu, Myriam Benamor, Annaig Le-Halpere, Philippe Truffinet, Marc Tardieu, Benedicte Dubois, Helene Verhelst, Veneta Bojinova-Tchamova, Jean Mah, Fang Fang, Yunpeng Hao, Li Jiang, Ling Li, Ding'An Mao, Wei Qiu, Guojun Tan, Ye Wu, Meini Zhang, Hongyu Zhou, Shuizhen Zhou, Katrin Gross-Paju, Emmanuel Cheuret, Giles Edan, Sandra Vukusic, George Chrousos, Dimitrios Zafeiriou, Anat Achiron, Adi Vaknin-Dembinsky, Bassem Yamout, Jurate Laurynaitiene, Nerija Vaiciene-Magistris, Vladimir Bojkovski, Vesna Trajkova, Sana Chaouki, Najib Kissani, Rinze Neuteboom, Filipe Palavra, Anna Belova, Alexey Boyko, Evgeny Evdoshenko, Ekaterina Kairbekova, Nadezhda Malkova, Maria Shumilina, Natalya Skripchenko, Dimitrije Nikolic, Jose Meca-Lallana, Chahnez Charfi Triki, Mhiri Chokri, Riadh Gouider, Banu Anlar, Ayse Semra Hiz, Egemen Idiman, Recai Turkoglu, Zuhal Yapici, Unsal Yilmaz, Lyudmyla Tantsura, Nataliia Voloshyna, Ming Lim, Evangeline Wassmer, Mark Cascione, Christopher LaGanke, Kevin Rathke, John Scagnelli
Publikováno v:
The Lancet Neurology, 20(12), 1001-1011. Lancet Publishing Group
Background: Therapeutic options for children with multiple sclerosis are scarce. Teriflunomide is approved in more than 80 countries for the treatment of adults with relapsing multiple sclerosis. The TERIKIDS study examined the safety and efficacy of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ccabed9102b9a00a1d52c5bf3629e63
https://pure.eur.nl/en/publications/9a1acc50-a431-44d3-9955-e7dcdc6b22c3
https://pure.eur.nl/en/publications/9a1acc50-a431-44d3-9955-e7dcdc6b22c3
Publikováno v:
The Pan African Medical Journal, Vol 20, Iss 3 (2015)
Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal re
Externí odkaz:
https://doaj.org/article/1e01905510a24508a6c227fc09efdd23
Publikováno v:
Case Reports in Pediatrics, Vol 2015 (2015)
Multicentric Castleman’s disease is a rare benign and unexplained lymphoproliferative disorder that is extremely uncommon in children. It presents with fever, systemic symptoms, generalized lymphadenopathy, and laboratory markers of inflammation. I
Externí odkaz:
https://doaj.org/article/d0d4830799e54825ab971c0261b3d25d
Autor:
Jihad Kassel, Zakia Douhi, Chaymae Jroundi, Hanane Baybay, Sara Elloudi, Fatima-Zahra Mernissi, Chaïmâa Benghabrit, Kenza Elmkadem, Sana Abourazzak, Sana Chaouki, Moustapha Hida
Publikováno v:
Our Dermatology Online. 13:e41-e41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::204c6aedd6bf8f5b608a83a19d3ab542
https://doi.org/10.7241/ourd.2022e.41
https://doi.org/10.7241/ourd.2022e.41