Implication of IL-12A, IL-12B, IL-6, and TNF single-nucleotide polymorphisms in severity and susceptibility to COVID-19 von Benmansour, R., Tagajdid, M. R., Lahlou, I. A, Oumzil, H., El Hamzaoui, H., Fjouji, S., Doghmi, N., Houba, A., Elkochri, S., Aabi, R., Elannaz, H., Laraqui, A., El Mchichi, B., Touil, N., Ennibi, K., Bouhouche, A.

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Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraple... von Bouhouche, A, Benomar, A, Bouslam, N, Chkili, T, Yahyaoui, M

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Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated w... von Azzedine, H., Bolino, A., Taïeb, T., Birouk, N., Di Duca, M., Bouhouche, A., Benamou, S., Mrabet, A., Hammadouche, T., Chkili, T., Gouider, R., Ravazzolo, R., Brice, A., Laporte, J., LeGuern, E.

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Association of vitamin D status with multiple sclerosis in a case-control study from Morocco von Skalli, A., Ait Ben Haddou, E.H., El Jaoudi, R., Razine, R., Mpandzou, G.A., Tibar, H., El Fahime, E., Bouslam, N., Alami, A., Benomar, A., Hajjout, K., Yahyaoui, M., Bouhouche, A.

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations von AZZEDINE, H, RAVISE, N, HAMADOUCHE, T, BOUHOUCHE, A, GUILBOT, A, STENDEL, C, RUBERG, M, BRICE, A, BIROUK, N, DUBOURG, O, TAZIR, M, LEGUERN, E, VERNY, C, GABRËELS-FESTEN, A, LAMMENS, M, GRID, D, VALLAT, J. M, DUROSIER, G, SENDEREK, J, NOUIOUA, S

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Characterization of Recessive Parkinson Disease in a Large Multicenter Study von Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Romdhan, Sawssan Ben, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Toullec, Benjamin Le, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohamed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Ben Romdhan, Sawssan, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Le Toullec, Benjamin, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Ben Djebara, Mouna, Gouider, Riadh, Tazir, Meriem, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andy, Corvol, Jean‐Christophe, Brice, Alexis

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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease von Dubourg, O, Azzedine, H, Verny, C, Durosier, G, Birouk, N, Gouider, R, Salih, M, Bouhouche, A, Thiam, A, Grid, D, Mayer, M, Ruberg, M, Tazir, M, Brice, A, LeGuern, E

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Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family von Cherkaoui Jaouad, I, El Alloussi, M, Laarabi, F.Z, Bouhouche, A, Ameziane, R, Sefiani, A

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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families von Bouhouche, Ahmed, Birouk, Nazha, Azzedine, Hamid, Benomar, Ali, Durosier, Garry, Ente, Dorothée, Muriel, Marie-Paule, Ruberg, Merle, Slassi, Ilham, Yahyaoui, Mohamed, Dubourg, Odile, Ouazzani, Reda, LeGuern, Eric

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Juvenile Huntington disease: A case study von Nejjari, I, Rhouda, H, Bouhouche, A, Kriouile, Y

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Hyperaldostéronisme primaire et syndrome de cushing infra clinique : une association rare von Bouhouche, A, Chikhi, B, Nacro, Y, Sellal, Z, Aribi, Y, Kemali, Z

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High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients von BOUHOUCHE, A, BENOMAR, A, BIROUK, N, BOUSLAM, N, OUAZZANI, R, YAHYAOUI, M, CHKILI, T

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G.P.11.12 Phenotypical features of 11 Moroccan families with autosomal recessive Charcot-Marie-Tooth disease associated with mutations in the GDAP1 gene von Bouhouche, A, Azzedine, H, Dubourg, O, Benomar, A, Belaidi, H, Yahyaoui, M, Le Guern, E, Ouazzani, R, Birouk, N

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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) von Bouslam, Naima, Benomar, Ali, Azzedine, Hamid, Bouhouche, Ahmed, Namekawa, Michito, Klebe, Stephan, Charon, Céline, Durr, Alexandra, Ruberg, Merle, Brice, Alexis, Yahyaoui, Mohamed, Stevanin, Giovanni

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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33 von GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LEGUERN, E.

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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33 von GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LeGUERN, E.

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Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1 von Bouhouche, Ahmed, Benomar, Ali, Bouslam, Naima, Ouazzani, Reda, Chkili, Taïeb, Yahyaoui, Mohamed

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Combination of Positional Cloning and New Generation Sequencing Identifies 3 Novel Genes in Spastic Paraplegia Involved in Common Metabolic Pathways (P01.205) von Stevanin, G., Tesson, C., Nawara, M., Salih, M., Zaki, M., Mundwiller, E., Al Balwi, M., Boukhris, A., Bouhouche, A., Martin, E., Elmalik, S., Alswaid, A., Mochel, F., Santorelli, F., Benomar, A., Al Rasheed, S., Mhiri, C., Gleeson, J., Darios, F., Durr, A., Brice, A.

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Modeling of ladle metallurgical treatment using neural networks von Bast, J., Bouhouche, S., Boucherit, M. S., Lahreche, M.

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A novel locus for autosomal recessive spastic ataxia on chromosome 17p von BOUSLAM, Naima, BOUHOUCHE, Ahmed, BRICE, Alexis, YAHYAOUI, Mohamed, STEVANIN, Giovanni, BENOMAR, Ali, HANEIN, Sylvain, KLEBE, Stephan, AZZEDINE, Hamid, DI GIANDOMENICO, Silvia, BOLAND-AUGE, Anne, SANTORELLI, Filippo M, DURR, Alexandra

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