TOC versus UV spectrophotometry for wastewater quality monitoring von Thomas, O, El Khorassani, H, Touraud, E, Bitar, H

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Minimisation strategy of petrochemical wastewater organic load von EL KHORASSANI, H, TREBUCHON, P, BITAR, H, THOMAS, O

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UV treatability test for chemical and petrochemical wastewater von Castillo, L., El Khorassani, H., Trebuchon, P., Thomas, O.

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UV treatability test for chemical and petrochemical wastewater von Castillo, L., Khorassani, H. El, Trebuchon, P., Thomas, O.

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A simple UV spectrophotometric procedure for the survey of industrial sewage system von El Khorassani, Houda, Trebuchon, P., Bitar, H., Thomas, O.

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A simple UV spectrophotometric procedure for the survey of industrial sewage system von EL KHORASSANI, H, TREBUCHON, P, BITAR, H, THOMAS, O

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Application of UV Spectrophotometry to the Study of Treated Wastewater Discharges in Rivers von El Khorassani, H., Theraulaz, F., Thomas, O.

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Immunogenicity, efficacy and safety of Nuwiq® (human‐cl rhFVIII) in previously untreated patients with severe haemophilia A—Interim results from the NuProtect Study von Liesner, R. J., Abashidze, M., Aleinikova, O., Altisent, C., Belletrutti, M. J., Borel‐Derlon, A., Carcao, M., Chambost, H., Chan, A. K. C., Dubey, L., Ducore, J., Fouzia, N. A., Gattens, M., Gruel, Y., Guillet, B., Kavardakova, N., El Khorassani, M., Klukowska, A., Lambert, T., Lohade, S., Sigaud, M., Turea, V., Wu, J. K. M., Vdovin, V., Pavlova, A., Jansen, M., Belyanskaya, L., Walter, O., Knaub, S., Neufeld, E. J.

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AB0903 Is There Any Relationship between the Children Health Assessment Questionnaire (CHAQ) and the European Quality of Life (EUROQOL) in Children Suffering from Chronic Haemophil... von Medrare, L., Ngeuleu, A., Rkain, M., Bouaddi, I., Znat, F., El Kabbaj, S., Lakhdar, T., Benslama, I., Rkain, H., Allali, F., Khattab, M., El Khorassani, M., Hajjaj-Hassouni, N.

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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination von Efthymiou, S, Salpietro, V, Malintan,N, Poncelet, M, Kriouile, Y, Fortuna, S, De Zorzi, R, Payne, K, Henderson, L.B, Cortese, A, Maddirevula, S, Alhashmi, N, Wiethoff, S, Ryten, M, Botia, J.A, Provitera, V, Schuelke, M, Vandrovcova, J, SYNAPS Study Group, Walsh, L, Torti, E, Iodice, V, Najafi, M, Karimiani, E.G, Maroofian, R, Siquier-Pernet, K, Boddaert, N, De Lonlay, P, Cantagrel, V, Aguennouz, M, El Khorassani, M, Schmidts, M, Alkuraya, F.S, Edvardson, S, Nolano, M, Devaux, J, Houlden, H, Cormand Rifà, Bru

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A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream von Robert-Ebadi, H, de Moerloose, P, Khorassani, M El, Khattab, M El, Neerman-Arbez, M

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The World Federation of Hemophilia World Bleeding Disorders Registry: insights from the first 10,000 patients von Coffin, Donna, Gouider, Emma, Konkle, Barbara, Hermans, Cedric, Lambert, Catherine, Diop, Saliou, Ayoub, Emily, Tootoonchian, Ellia, Youttananukorn, Toong, Dakik, Pamela, Pereira, Ticiana, Iorio, Alfonso, Pierce, Glenn F

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AB0903 Is There Any Relationship between the Children Health Assessment Questionnaire (CHAQ) and the European Quality of Life (EUROQOL) in Children Suffering from Chronic Haemophil... von Medrare, L., Ngeuleu, A., Rkain, M., Bouaddi, I., Znat, F., El Kabbaj, S., Lakhdar, T., Benslama, I., Rkain, H., Allali, F., Khattab, M., El Khorassani, M., Hajjaj-Hassouni, N.

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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome von Salpietro, V, Maroofian, R, Zaki, MS, Wangen, J, Ciolfi, A, Barresi, S, Efthymiou, S, Lamaze, A, Aughey, GN, Al Mutairi, F, Rad, A, Rocca, C, Calì, E, Accogli, A, Zara, F, Striano, P, Mojarrad, M, Tariq, H, Giacopuzzi, E, Taylor, JC, Oprea, G, Skrahina, V, Rehman, KU, Abd Elmaksoud, M, Bassiony, M, El Said, HG, Abdel-Hamid, MS, Al Shalan, M, Seo, G, Kim, S, Lee, H, Khang, R, Issa, MY, Elbendary, HM, Rafat, K, Marinakis, NM, Traeger-Synodinos, J, Ververi, A, Sourmpi, M, Eslahi, A, Khadivi Zand, F, Beiraghi Toosi, M, Babaei, M, Jackson, A, Hannah, MG, Bugiardini, E, Bertini, E, Kriouile, Y, El-Khorassani, M, Aguennouz, M, Groppa, S, Karashova, BM, Goraya, JS, Sultan, T, Avdjieva, D, Kathom, H, Tincheva, R, Banu, S, Veggiotti, P, Verrotti, A, Lanari, M, Savasta, S, Macaya, A, Garavaglia, B, Borgione, E, Papacostas, S, Vikelis, M, Chelban, V, Kaiyrzhanov, R, Cortese, A, Sullivan, R, Papanicolaou, EZ, Dardiotis, E, Maqbool, S, Ibrahim, S, Kirmani, S, Rana, NN, Atawneh, O, Lim, SY, Zuccotti, GV, Marseglia, GL, Esposito, S, Shaikh, F, Cogo, P, Corsello, G, Mangano, S, Nardello, R, Mangano, D, Scardamaglia, A, Koutsis, G, Scuderi, C, Ferrara, P, Morello, G, Zollo, M, Berni-Canani, R, Terracciano, LM, Sisto, A, Di Fabio, S, Strano, F, Scorrano, G

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A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration von Efthymiou, S, Kriouile, Y, Salpietro, V, Hajar, R, Ghizlane, Z, Mankad, K, El Khorassani, M, Aguennouz, M, Houlden, H, Wiethoff, S

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Hemophilia in a newborn with an unusual clinical presentation von Barkat, A, Kabiri, M, Zaari, Y, Ghazali, H, Karboubi, L, El Khorassani, M, Lamdouar Bouazzaoui, N

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A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease von Calì, E, Lin, SJ, Rocca, C, Sahin, Y, Al Shamsi, A, El Chehadeh, S, Chaabouni, M, Mankad, K, Galanaki, E, Efthymiou, S, Sudhakar, S, Athanasiou-Fragkouli, A, Çelik, T, Narlı, N, Bianca, S, Murphy, D, De Carvalho Moreira, FM, Hannah, MG, Bugiardini, E, Kriouile, Y, El Khorassani, M, Aguennouz, M, Groppa, S, Karashova, BM, Di Rosa, G, Goraya, JS, Sultan, T, Avdjieva, D, Kathom, H, Tincheva, R, Banu, S, Veggiotti, P, Verrotti, A, Savasta, S, Ruiz, AM, Garavaglia, B, Borgione, E, Papacostas, S, Compagnoni, C, Piccirilli, A, Vikelis, M, Chelban, V, Kaiyrzhanov, R, Cortese, A, Sullivan, R, Papanicolaou, EZ, Dardiotis, E, Maqbool, S, Ibrahim, S, Kirmani, S, Rana, NN, Atawneh, O, Lim, SY, Shaikh, F, Scardamaglia, A, Koutsis, G, Mangano, S, Scuderi, C, Morello, G, Zollo, M, Heimer, G, Striano, P, Al-Khawaja, I, Al-Mutairi, F, Alkuraya, FS, Rizig, M, Shashkin, C, Zharkynbekova, N, Koneyev, K, Manizha, G, Isrofilov, M, Guliyeva, U, Salayev, K, Khachatryan, S, Xiromerisiou, G, Spanaki, C, Tucci, A, Fiorillo, C, Rissotto, F, Munell, F, Gagliano, A, Jan, F, Chimenz, R, Gitto, E, Cuppari, C, Romeo, C, Magrinelli, F, Gupta, N, Kabra, M, Benrhouma, H, Tazir, M, Zagaroli, L, Caloisi, C, Fabiano, C, Bottone, G, Farello, G, Di Fabio, S, Obeid, M, Bakhtadze, S, Saadi, NW

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Deux présentations néonatales inhabituelles de l’hémophilie von Barkat, A., Kabiri, M., Zaari, Y., Ghazali, H., Karboubi, L., El khorassani, M., Lamdouar Bouazzaoui, N.

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A simple UV spectrophotometry procedure for the survey of industrial sewage system von Khorassani, Houda El, Trebuchon, P., Bitar, H., Thomas, O.

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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination von Efthymiou, S, Salpietro, V, Malintan, N, Poncelet, M, Kriouile, Y, Fortuna, S, De Zorzi, R, Payne, K, Henderson, LB, Cortese, A, Maddirevula, S, Alhashmi, N, Wiethoff, S, Ryten, M, Botia, JA, Provitera, V, Schuelke, M, Vandrovcova, J, SYNAPS Study Group, Walsh, L, Torti, E, Iodice, V, Najafi, M, Karimiani, EG, Maroofian, R, Siquier-Pernet, K, Boddaert, N, De Lonlay, P, Cantagrel, V, Aguennouz, M, El Khorassani, M, Schmidts, M, Alkuraya, FS, Edvardson, S, Nolano, M, Devaux, J, Houlden, H

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