Search Results - "Ghaber, S."

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients by Mahmoud, Taher, Sahli, Chaima, Hadj Fredj, Sondess, Amri, Yessine, Othmani, Rim, Mohamed, Ghaber S., Zein, Ekhtelbenina, Messaoud, Taieb

“…Background Hemoglobinopathies, inherited disorders of hemoglobin (Hb), are the most common hereditary monogenic diseases of the red cell in the world. Few…”
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Sensitivity to antibiotics uropathogens bacteria in Nouakchott - Mauritania by Hailaji, N S M, Ould Salem, M L, Ghaber, S M

“…A urinary tract infection (UTI) is a frequent pathology in outpatients and admitted patients as well. In recent years, there has been an increase in the…”
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Frequencies and ethnic distribution of ABO and Rh(D) blood groups in Mauritania: results of first nationwide study by Hamed, C. T., Bollahi, M. A., Abdelhamid, I., Med Mahmoud, M. A., BA, B., Ghaber, S., Habti, N., Houmeida, A.

“…Summary There is no data available on the ABO/Rh(D) frequencies in the Mauritanian population. We retrospectively analysed records of a 5‐year database that…”
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Osteoporosis-Pseudoglioma in a Mauritanian Child due to a Novel Mutation in LRP5 by Collet, Corinne, Hacen, M. M., Ghaber, S. M., Biha, Noura

“…Osteoporosis-pseudoglioma (OPPG) syndrome is a very rare autosomal recessive disorder, caused by mutations in the low-density lipoprotein receptor-related…”
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Troubles du métabolisme minéral et osseux chez les patients hémodialysés chroniques en Mauritanie : évaluation de l’adhésion aux recommandations internationales (KDOQI et KDIGO) by Sidi Aly, A., Mah, S.M., Mohamed Lamine Sidina, S., Lemrabott, M., Beddi, M.L., Emeyen, O.E., Ghaber, S.

“…Les troubles du métabolisme minéral et osseux constituent l’une des complications fréquentes et graves de l’insuffisance rénale chronique (IRC). Les objectifs…”
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