Implication of IL-12A, IL-12B, IL-6, and TNF single-nucleotide polymorphisms in severity and susceptibility to COVID-19
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
Published in International journal of immunopathology and pharmacology (01.01.2024)
Published in International journal of immunopathology and pharmacology (01.01.2024)
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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 paraplegia
Bouhouche, A, Benomar, A, Bouslam, N, Chkili, T, Yahyaoui, M
Published in Journal of medical genetics (01.05.2006)
Published in Journal of medical genetics (01.05.2006)
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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 with Early-Onset Glaucoma
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.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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Association of vitamin D status with multiple sclerosis in a case-control study from Morocco
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.
Published in Revue neurologique (01.03.2018)
Published in Revue neurologique (01.03.2018)
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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
Azzedine, H, Ravisé, N, Verny, C, Gabrëels-Festen, A, Lammens, M, Grid, D, Vallat, J M, Durosier, G, Senderek, J, Nouioua, S, Hamadouche, T, Bouhouche, A, Guilbot, A, Stendel, C, Ruberg, M, Brice, A, Birouk, N, Dubourg, O, Tazir, M, LeGuern, E
Published in Neurology (22.08.2006)
Published in Neurology (22.08.2006)
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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease
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
Published in Neuromolecular medicine (01.03.2006)
Published in Neuromolecular medicine (01.03.2006)
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Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families
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
Published in Brain (London, England : 1878) (01.04.2007)
Published in Brain (London, England : 1878) (01.04.2007)
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Juvenile Huntington disease: A case study
Nejjari, I, Rhouda, H, Bouhouche, A, Kriouile, Y
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.10.2013)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.10.2013)
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Hyperaldostéronisme primaire et syndrome de cushing infra clinique : une association rare
Bouhouche, A, Chikhi, B, Nacro, Y, Sellal, Z, Aribi, Y, Kemali, Z
Published in Annales d'endocrinologie (01.10.2014)
Published in Annales d'endocrinologie (01.10.2014)
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High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients
BOUHOUCHE, A, BENOMAR, A, BIROUK, N, BOUSLAM, N, OUAZZANI, R, YAHYAOUI, M, CHKILI, T
Published in Journal of neurology (01.10.2003)
Published in Journal of neurology (01.10.2003)
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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
Bouhouche, A, Azzedine, H, Dubourg, O, Benomar, A, Belaidi, H, Yahyaoui, M, Le Guern, E, Ouazzani, R, Birouk, N
Published in Neuromuscular disorders : NMD (2007)
Published in Neuromuscular disorders : NMD (2007)
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The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33
GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LEGUERN, E.
Published in Annals of the New York Academy of Sciences (01.10.1999)
Published in Annals of the New York Academy of Sciences (01.10.1999)
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Journal Article
The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33
GUILBOT, A., KESSALI, M., RAVISÉ, N., HAMMADOUCHE, T., BOUHOUCHE, A., MAISONOBE, T., GRID, D., BRICE, A., LeGUERN, E.
Published in Annals of the New York Academy of Sciences (01.10.1999)
Published in Annals of the New York Academy of Sciences (01.10.1999)
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Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)
Bouslam, Naima, Benomar, Ali, Azzedine, Hamid, Bouhouche, Ahmed, Namekawa, Michito, Klebe, Stephan, Charon, Céline, Durr, Alexandra, Ruberg, Merle, Brice, Alexis, Yahyaoui, Mohamed, Stevanin, Giovanni
Published in Annals of neurology (01.04.2005)
Published in Annals of neurology (01.04.2005)
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Journal Article
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1
BOUHOUCHE, Ahmed, BENOMAR, Ali, BOUSLAM, Naima, OUAZZANI, Reda, CHKILI, Taieb, YAHYAOUI, Mohamed
Published in European journal of human genetics : EJHG (01.02.2006)
Published in European journal of human genetics : EJHG (01.02.2006)
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Maladie de Huntington juvénile : à propos d’un cas
Nejjari, I., Rhouda, H., Bouhouche, A., Kriouile, Y.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.10.2013)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.10.2013)
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