Mucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjects
ALIF, N., HESS, K., STRACZEK, J., SEBBAR, S., N'BOU, A., NABET, P., DOUSSET, B.
Published in Annals of human genetics (01.01.1999)
Published in Annals of human genetics (01.01.1999)
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0121 : Predictors of cardiovascular mortality factors in elderly patients over 75 years hospitalized in cardiology intensive care unit
Bouzouba, Laila, Houari, Chaimaa, Almamy, Brahim, Sebbar, S., Fikal, N., Kapche Fotso, D.M., Bennouna, Ghali, Azzouzi, L., Habbal, R.
Published in Archives of Cardiovascular Diseases Supplements (01.04.2015)
Published in Archives of Cardiovascular Diseases Supplements (01.04.2015)
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0120 : Prognostic value of elevated LV filling pressures in the acute phase of myocardial infarction
Bouzouba, Laila, Houari, Chaimaa, Sebbar, S., Almamy, Brahim, Fikal, N., Kapche Fotso, D.M., Bennouna, Ghali, Azzouzi, L., Habbal, R.
Published in Archives of Cardiovascular Diseases Supplements (01.04.2015)
Published in Archives of Cardiovascular Diseases Supplements (01.04.2015)
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Mucopolysaccharidose de type I au Maroc: manifestations cliniques et profil génétique
Alif, N., Hess, K., Straczek, J., Sebbar, S., Belahsen, Y., Mouane, N., Abkari, A., Nabet, P., Gelot, M.A.
Published in Archives de pédiatrie (Paris) (01.06.2000)
Published in Archives de pédiatrie (Paris) (01.06.2000)
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Journal Article
Conference Proceeding
Mucopolysaccharidosis type I in Morocco: clinical features and genetic profile
Alif, N, Hess, K, Straczek, J, Sebbar, S, Belahsen, Y, Mouane, N, Abkari, A, Nabet, P, Gelot, M A
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.06.2000)
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Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.06.2000)
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