The prevalence of anti-factor VIII and anti-factor IX antibodies among patients with hemophilia in Rabat, Morocco: a single center experience by Bouyadmar, Meryem, Khorassani, Mohamed El, Kababri, Maria El, Kili, Amina, Hessissen, Laila

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Time to diagnosis of pediatric brain tumors: a report from the Pediatric Hematology and Oncology Center in Rabat, Morocco by Boutahar, Fatima Zahra, Benmiloud, Sarra, El Kababri, Maria, Kili, Amina, El Khorassani, Mohamed, Allali, Nazik, Khattab, Mohamed, Qaddoumi, Ibrahim, Hessissen, Laila

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A rare presentation of a spinal diffuse midline glioma in a child: a case report by Isfaoun, Zineb, Laasri, Khadija, Jidal, Manal, Cherradi, Nadia, Melhaoui, Adil, Chat, Latifa, Haddad, Siham El, Kababri, Maria El, Khorassani, Mohamed El, Kili, Amina, Ansari, Naoual El, Hessissen, Laila

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Von Willebrand's disease: case report and review of literature by Echahdi, Hanae, El Hasbaoui, Brahim, El Khorassani, Mohamed, Agadr, Aomar, Khattab, Mohamed

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Clinical pharmacology, efficacy and safety study of a triple‐secured fibrinogen concentrate in adults and adolescent patients with congenital fibrinogen deficiency by Djambas Khayat, Claudia, El Khorassani, Mohamed, Lambert, Thierry, Gay, Valérie, Barthez‐Toullec, Malika, Lamazure, Jennifer, Bellon, Anne, Henriet, Céline, Bridey, Françoise, Négrier, Claude

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REACH: A programme for improving care in haemophilia by Goga, Yasmin, Boukari, Rachida, Bensadok, Meriem, El Khorassani, Mohamed, Khelif, Abderrahim, Al Rawas, Abdulhakim, Alkasim, Fawaz, Shaheen, Naglaa Mohamad, Negrier, Claude

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Overview of Sickle-cell disease management in the Pediatric Hematology and Oncology Center of Rabat (Morocco) by El kababri, Maria, Lakhrissi, Meryem, Isfaoun, Zineb, El ansari, Naoual, Kili, Amina, El khorassani, Mohamed, Khattab, Mohammed, Thuret, Isabelle, Hessissen, Laila

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Un cas marocain d’érythrophagocytose blastique et LAL T de novo sans anomalie cytogénétique by Kahouli, Sophia, Zahid, Hafid, khorassani, Mohamed El, kabbaj, Saâd El, Benkirane, Majid, Messaoudi, Nezha

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Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment by Salpietro, Vincenzo, Malintan, Nancy T., Llano-Rivas, Isabel, Spaeth, Christine G., Efthymiou, Stephanie, Striano, Pasquale, Vandrovcova, Jana, Cutrupi, Maria C., Chimenz, Roberto, David, Emanuele, Di Rosa, Gabriella, Marce-Grau, Anna, Raspall-Chaure, Miquel, Martin-Hernandez, Elena, Zara, Federico, Minetti, Carlo, Salpietro, Vincenzo, Efthymiou, Stephanie, Kriouile, Yamna, El Khorassani, Mohamed, Aguennouz, Mhammed, Karashova, Blagovesta, Avdjieva, Daniela, Kathom, Hadil, Tincheva, Radka, Van Maldergem, Lionel, Nachbauer, Wolfgang, Boesch, Sylvia, Arning, Larissa, Timmann, Dagmar, Cormand, Bru, Pérez-Dueñas, Belen, Di Rosa, Gabriella, Pironti, Erica, Goraya, Jatinder S., Sultan, Tipu, Kirmani, Salman, Ibrahim, Shahnaz, Jan, Farida, Mine, Jun, Banu, Selina, Veggiotti, Pierangelo, Ferrari, Michel D., Verrotti, Alberto, Marseglia, Gian Luigi, Savasta, Salvatore, Garavaglia, Barbara, Scuderi, Carmela, Borgione, Eugenia, Dipasquale, Valeria, Cutrupi, Maria Concetta, Portaro, Simona, Sanchez, Benigno Monteagudo, Pineda-Marfa’, Mercedes, Munell, Francina, Macaya, Alfons, Boles, Richard, Heimer, Gali, Papacostas, Savvas, Manole, Andreea, Malintan, Nancy, Zanetti, Maria Natalia, Hanna, Michael G., Rothman, James E., Kullmann, Dimitri M., Houlden, Henry, Bello, Oscar D., De Zorzi, Rita, Fortuna, Sara, Dauber, Andrew, Alkhawaja, Mariam, Sultan, Tipu, Mankad, Kshitij, Vitobello, Antonio, Thomas, Quentin, Mau-Them, Frederic Tran, Faivre, Laurence, Martinez-Azorin, Francisco, Prada, Carlos E., Macaya, Alfons, Kullmann, Dimitri M., Rothman, James E., Krishnakumar, Shyam S., Houlden, Henry

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Micturition Hypertension in an Adolescent by Jakamy, Réda, Ugoani, Elizabeth O., El Khorassani, Mohamed, Ibat, Driss, Oulahyane, Rachid

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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination by Efthymiou, Stephanie, Salpietro, Vincenzo, Malintan, Nancy, Poncelet, Mallory, Kriouile, Yamna, Fortuna, Sara, De Zorzi, Rita, Payne, Katelyn, Henderson, Lindsay B, Cortese, Andrea, Maddirevula, Sateesh, Alhashmi, Nadia, Wiethoff, Sarah, Ryten, Mina, Botia, Juan A, Provitera, Vincenzo, Schuelke, Markus, Vandrovcova, Jana, Walsh, Laurence, Torti, Erin, Iodice, Valeria, Najafi, Maryam, Karimiani, Ehsan Ghayoor, Maroofian, Reza, Siquier-Pernet, Karine, Boddaert, Nathalie, De Lonlay, Pascale, Cantagrel, Vincent, Aguennouz, Mhammed, El Khorassani, Mohamed, Schmidts, Miriam, Alkuraya, Fowzan S, Edvardson, Simon, Nolano, Maria, Devaux, Jérôme, Houlden, Henry

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A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration by Efthymiou, Stephanie, Kriouile, Yamna, Salpietro, Vincenzo, Hajar, Rhouda, Ghizlane, Zouiri, Mankad, Kshitij, El Khorassani, Mohamed, Aguennouz, Mhammed, Houlden, Henry, Wiethoff, Sarah

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Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder by Aughey, Gabriel N, Cali, Elisa, Maroofian, Reza, Zaki, Maha S, Pagnamenta, Alistair T, Ali, Zafar, Abdulllah, Uzma, Rahman, Fatima, Menzies, Lara, Shafique, Anum, Suri, Mohnish, Roze, Emmanuel, Aguennouz, Mohammed, Ghizlane, Zouiri, Saadi, Saadia Maryam, Fatima, Ambrin, Cheema, Huma Arshad, Anjum, Muhammad Nadeem, Morel, Godelieve, Robin, Stephanie, McFarland, Robert, Altunoglu, Umut, Kraus, Verena, Shoukier, Moneef, Murphy, David, Flemming, Kristina, Yttervik, Hilde, Rhouda, Hajar, Lesca, Gaetan, Chatron, Nicolas, Rossi, Massimiliano, Murtaza, Bibi Nazia, Ur Rehman, Mujaddad, Lord, Jenny, Giacopuzzi, Edoardo, Hayat, Azam, Siraj, Muhammad, Badv, Reza Shervin, Seo, Go Hun, Beetz, Christian, Kayserili, Hülya, Krioulie, Yamna, Chung, Wendy K, Naz, Sadaf, Maqbool, Shazia, Chandler, Kate, Kershaw, Christopher, Wright, Thomas, Banka, Siddharth, Gleeson, Joseph G, Taylor, Jenny C, Efthymiou, Stephanie, Baig, Shahid Mahmood, Severino, Mariasavina, Jepson, James E C, Houlden, Henry

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Un cas marocain d´érythrophagocytose blastique et LAL T de novo sans anomalie cytogénétique by Kahouli, Sophia, Zahid, Hafid, El Khorassani, Mohamed, El Kabbaj, Saâd, Benkirane, Majid, Messaoudi, Nezha

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Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature by Chebihi, Zahra Takki, Belkhayat, Aziza, Chadli, Elbekkay, Hilal, Latifa, Skhoun, Hanaa, Hessissen, Laila, El Khorassani, Mohamed, El Kababri, Maria, Kili, Amina, Khattab, Mohammed, Bakri, Youssef, Dakka, Nadia

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Erythrophagocytosis by blast cells and de novo T cell LAL without cytogenetic abnormalities in a Moroccan patient by Kahouli, Sophia, Zahid, Hafid, Khorassani, Mohamed El, Kabbaj, Saâd El, Benkirane, Majid, Messaoudi, Nezha

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Substrate Integrated Waveguide Symmetrical Window Bandpass Filter for Satellite Applications by Badaoui, Imane, Touhami, Naima Amar, Moubadir, Mahmoud, El Khorassani, Mohamed Taha

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Inhibitor Development in Previously Untreated Patients with Severe Hemophilia a Treated with Nuwiq®, a New Generation Recombinant FVIII of Human Origin by Liesner, Raina, Abashidze, Marina, Aleinikova, Olga, Altisent, Carmen, Belletrutti, Mark J., Borel-Derlon, Annie, Carcao, Manuel, Chambost, Hervé, Chan, Anthony, Dubey, Leonid, Ducore, Jonathan M., Abubacker, Fouzia Nambiathayil, Gattens, Michael, Gruel, Yves, Kavardakova, Natalya, Khorassani, Mohamed, Klukowska, Anna, Königs, Christoph, Lambert, Thierry, Lohade, Sunil, Sigaud, Marianne, Turea, Valentin, Wu, John K., Vdovin, Vladimir

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Pediatric rhabdomyosarcoma in Morocco by Hessissen, Laila, Kanouni, Lamya, Kili, Amina, Nachef, Mohamed Nacer, El Khorassani, Mohamed, Benjaafar, Noureddine, Khattab, Mohamed, El Gueddari, Brahim El Khalil

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Un cas marocain d´érythrophagocytose blastique et LAL T de novo sans anomalie cytogénétique by Sophia Kahouli, Hafid Zahid, Mohamed El khorassani, Saâd El kabbaj, Majid Benkirane, Nezha Messaoudi

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