Unusual presentation of chronic headaches revealing osteopetrosis: A case report von Erradi, Mariam, Sediki, Soukaina, Chaouki, Sana, Hida, Moustapha

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The Genetic Facets of Dravet Syndrome: Recent Insights von Mouhi, Hinde El, Abbassi, Meriame, Jalte, Meryem, Natiq, Abdelhafid, Bouguenouch, Laila, Chaouki, Sana

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Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moro... von El Mouhi, Hinde, Abbassi, Meriame, Sayel, Hanane, Trhanint, Said, Natiq, Abdelhafid, El Hejjioui, Brahim, Jalte, Merym, Ahmadi, Youssef, Chaouki, Sana

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The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study von Ahakoud, Mohamed, Daha Belghiti, Hanae, Nedbour, Ayoub, Bouramtane, Abdelhamid, Chaouki, Sana, Bouguenouch, Laila, Ouldim, Karim

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Children’s poisoning profile during the Covid-19 pandemic – Experience of Hassan II University Hospital in Fez, MOROCCO von Sahar, Amrani Hanchi, Hasnae, Hoummani, Hajar, Mourabiti, Mohammed, Chebaibi, Sana, Chaouki, Sanae, Achour, Ilham, Tadmouri, Moustapha, Hida

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Cutis Laxa syndrome: a case report von Hbibi, Mohamed, Abourazzak, Sana, Idrissi, Mounia, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

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Multicentric Castleman’s Disease in a Child Revealed by Chronic Diarrhea von Hida, Moustapha, Atmani, Samir, Chaouki, Sana, Benmiloud, Sarra

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Syndrome d’activation macrophagique révélant un lymphome T sous-cutané chez un adolescent de 16 ans von Hbibi Mohamed, Benmiloud Sara, Rahmouni Safae, Tadmouri Ilhame, Abourazzak Sana, Chaouki Sana, Souilmi Fatima Zahra, Idrissi, Mounia Lakhdar, Hida Mostapha

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Hodgkin’s Lymphoma Revealed by Hemophagocytic Lymphohistiocytosis in a Child von Abourazzak, Sana, Chaouki, Sana, Hbibi, Mohamed, Benmiloud, Sarra, Hida, Moustapha

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Identification of novel and de novo variant in the SCN1A gene confirms Dravet syndrome in Moroccan child: a case report von El Mouhi, Hinde, Amllal, Nada, Abbassi, Meriame, Nedbour, Ayoub, Jalte, Meryem, Lyahyai, Jaber, Chafai Elalaoui, Siham, Bouguenouch, Laila, Chaouki, Sana

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Farber Disease in a Newborn von Sana, Chaouki, Larbi, Elarqam, Samir, Atmani, Abdelhak, Bouharrou, Mustapha, Hida

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Safety and efficacy of teriflunomide in paediatric multiple sclerosis (TERIKIDS): a multicentre, double-blind, phase 3, randomised, placebo-controlled trial von Chitnis, Tanuja, Banwell, Brenda, Kappos, Ludwig, Arnold, Douglas L, Gücüyener, Kivilcim, Deiva, Kumaran, Skripchenko, Natalia, Cui, Li-Ying, Saubadu, Stephane, Hu, Wenruo, Benamor, Myriam, Le-Halpere, Annaig, Truffinet, Philippe, Tardieu, Marc, Dubois, Benedicte, Verhelst, Helene, Bojinova-Tchamova, Veneta, Mah, Jean, Cui, Li-Ying, Fang, Fang, Hao, Yunpeng, Jiang, Li, Li, Ling, Mao, Ding'An, Qiu, Wei, Tan, Guojun, Wu, Ye, Zhang, Meini, Zhou, Hongyu, Zhou, Shuizhen, Gross-Paju, Katrin, Cheuret, Emmanuel, Deiva, Kumaran, Edan, Giles, Vukusic, Sandra, Chrousos, George, Zafeiriou, Dimitrios, Achiron, Anat, Vaknin-Dembinsky, Adi, Yamout, Bassem, Laurynaitiene, Jurate, Vaiciene-Magistris, Nerija, Bojkovski, Vladimir, Trajkova, Vesna, Chaouki, Sana, Kissani, Najib, Neuteboom, Rinze, Palavra, Filipe, Belova, Anna, Boyko, Alexey, Evdoshenko, Evgeny, Kairbekova, Ekaterina, Malkova, Nadezhda, Shumilina, Maria, Skripchenko, Natalya, Nikolic, Dimitrije, Meca-Lallana, Jose, Triki, Chahnez Charfi, Chokri, Mhiri, Gouider, Riadh, Anlar, Banu, Gücüyener, Kivilcim, Hiz, Ayse Semra, Idiman, Egemen, Turkoglu, Recai, Yapici, Zuhal, Yilmaz, Unsal, Tantsura, Lyudmyla, Voloshyna, Nataliia, Lim, Ming, Wassmer, Evangeline, Cascione, Mark, Chitnis, Tanuja, LaGanke, Christopher, Rathke, Kevin, Scagnelli, John

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Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic Patterns von Nmer, Samira, Ameli, Amina, Trhanint, Said, Chaouki, Sana, Bouguenouch, Laila, Ouldim, Karim

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Pyoderma gangrenosum: About a pediatric presentation von Kassel, Jihad, Douhi, Zakia, Jroundi, Chaymae, Baybay, Hanane, Elloudi, Sara, Mernissi, Fatima-Zahra, Benghabrit, Chaïmâa, Elmkadem, Kenza, Abourazzak, Sana, Chaouki, Sana, Hida, Moustapha

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Marqueurs chromosomiques: à propos d'un cas von Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, El Otmani, Ihsan, El Omairi, Nissrine, Chaouki, Sana, Hida, Moustapha, Ouldim, Karim

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Macrophage activation syndrome revealing subcutaneous T-cell lymphoma in a 16-year old adolescent von Hbibi, Mohamed, Benmiloud, Sara, Rahmouni, Safae, Tadmouri, Ilhame, Abourazzak, Sana, Chaouki, Sana, Souilmi, Fatima Zahra, Idrissi, Mounia Lakhdar, Hida, Mostapha

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Syndrome d’activation macrophagique révélant un lymphome T sous-cutané chez un adolescent de 16 ans von Hbibi, Mohamed, Benmiloud, Sara, Rahmouni, Safae, Tadmouri, Ilhame, Abourazzak, Sana, Chaouki, Sana, Zahra, Fatima Souilmi, Idrissi, Mounia Lakhdar, Hida, Mostapha

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Le syndrome de Cri du Chat : A propos d’une observation von Ouldim, Karim, Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, Otmani, Ihsan El, Hbibi, Mohamed, Chaouki, Sana, Hida, Moustapha

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Syndromes microdélétionnels (syndrome de Williams et syndrome de la délétion 22q11) au CHU Hassan II de Fès: à propos de 3 observations von Ouldim, Karim, Bouguenouch, Laila, Samri, Imane, El Otmani, Ihsan, Hamdaoui, Hasna, Bennis, Sanae, Lakhdar, Mounia Idrissi, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

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Gelastic seizures and fever originating from a parietal cortical dysplasia von Chaouki, Sana, Boujraf, Saïd, Atmani, Samir, Elarqam, Larbi, Messouak, Wafae

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