Neonatal screening of G6PD deficiency in Tunisia
Guellouz, N, Ben Mansour, I, Ouederni, M, Jabnoun, S, Kacem, S, Mokrani, Ch, Kastally, R, Chahed, M K, Khrouf, N
Published in Archives de l'Institut Pasteur de Tunis (2010)
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Published in Archives de l'Institut Pasteur de Tunis (2010)
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A family study of congenital malabsorption of folate
Jebnoun, S., Kacem, S., Mokrani, Ch, Chabchoub, A., Khrouf, N., Zittoun, J.
Published in Journal of inherited metabolic disease (01.11.2001)
Published in Journal of inherited metabolic disease (01.11.2001)
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Journal Article
DEPISTAGE NEONATAL DU DEFICIT EN G6PD EN TUNISIE
GUELLOUZ, N, MANSOUR, I. Ben, OUEDERNI, M, JABNOUN, S, KACEM, S, MOKRANI, Ch, KASTALLY, R, CHAHED, M. K, KHROUF, N
Published in Archives de l'Institut Pasteur de Tunis (2010)
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Published in Archives de l'Institut Pasteur de Tunis (2010)
Journal Article
Maladie des inclusions microvillositaires à manifestation anténatale : à propos de trois observations familiales
Guellouz Najjar, N., Zekri, S., Youssef, A., Zghal, D., Ben Hariz, M., Kefi, R., Ben Amara, F., Kacem, S., Mokrani, Ch, Jaafour, M.H., Zouari, F., Rzigua, H., Abdelhak, N.S., Jebnoun, S., Khrouf, N.
Published in Journal de pédiatrie et de puériculture (01.04.2011)
Published in Journal de pédiatrie et de puériculture (01.04.2011)
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Journal Article