Le syndrome d'apert

por Benmiloud, Sarra, Chaouki, Sana, Atmani, Samir, Hida, Moustapha
Publicado 2013

Multicentric Castleman's Disease in a Child Revealed by Chronic Diarrhea

por Benmiloud, Sarra, Chaouki, Sana, Atmani, Samir, Hida, Moustapha
Publicado 2015

Gelastic seizures and fever originating from a parietal cortical dysplasia

por Chaouki, Sana, Boujraf, Saïd, Atmani, Samir, Elarqam, Larbi, Messouak, Wafae
Publicado 2013

Hodgkin's Lymphoma Revealed by Hemophagocytic Lymphohistiocytosis in a Child

por Benmiloud, Sarra, Hbibi, Mohamed, Chaouki, Sana, Abourazzak, Sana, Hida, Moustapha
Publicado 2014

Cutis Laxa syndrome: a case report

por Hbibi, Mohamed, Abourazzak, Sana, Idrissi, Mounia, Chaouki, Sana, Atmani, Samir, Hida, Moustapha
Publicado 2015

The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study

por Ahakoud, Mohamed, Daha Belghiti, Hanae, Nedbour, Ayoub, Bouramtane, Abdelhamid, Chaouki, Sana, Bouguenouch, Laila, Ouldim, Karim
Publicado 2023

Le syndrome de Cri du Chat : A propos d’une observation

por Ouldim, Karim, Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, Otmani, Ihsan El, Hbibi, Mohamed, Chaouki, Sana, Hida, Moustapha
Publicado 2012

Marqueurs chromosomiques: à propos d'un cas

por Samri, Imane, Bouguenouch, Laila, Hamdaoui, Hasna, El Otmani, Ihsan, El Omairi, Nissrine, Chaouki, Sana, Hida, Moustapha, Ouldim, Karim
Publicado 2013

L'encéphalomyélite aiguë disséminée chez l'enfant

por Tadmori, Ilham, Chaouki, Sana, Abourazzak, Sana, Zahra, Souilmi Fatima, Benmiloud, Sarra, Idrissi, Mounia Lakhdar, Atmani, Samir, Hida, Moustapha
Publicado 2014

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...

por El Mouhi, Hinde, Abbassi, Meriame, Sayel, Hanane, Trhanint, Said, Natiq, Abdelhafid, El Hejjioui, Brahim, Jalte, Merym, Ahmadi, Youssef, Chaouki, Sana
Publicado 2023

Syndrome d’activation macrophagique révélant un lymphome T sous-cutané chez un adolescent de 16 ans

por Hbibi, Mohamed, Benmiloud, Sara, Rahmouni, Safae, Tadmouri, Ilhame, Abourazzak, Sana, Chaouki, Sana, Souilmi, Fatima Zahra, Idrissi, Mounia Lakhdar, Hida, Mostapha
Publicado 2018

Syndromes microdélétionnels (syndrome de Williams et syndrome de la délétion 22q11) au CHU Hassan II de Fès: à propos de 3 observations

por Ouldim, Karim, Bouguenouch, Laila, Samri, Imane, El Otmani, Ihsan, Hamdaoui, Hasna, Bennis, Sanae, Lakhdar, Mounia Idrissi, Chaouki, Sana, Atmani, Samir, Hida, Moustapha
Publicado 2012