Search Results - "Troudi, Monia"

Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1 genes by Elhayek, Donia, Perez de Nanclares, Gustavo, Chouchane, Slaheddine, Hamami, Saber, Mlika, Adnène, Troudi, Monia, Leban, Nadia, Ben Romdane, Wafa, Gueddiche, Mohamed Neji, El Amri, Féthi, Mrabet, Samir, Ben Chibani, Jemni, Castaño, Luis, Haj Khelil, Amel, Ariceta, Gema

“…Primary distal renal tubular acidosis (dRTA) caused by mutations in the genes that codify for the H + -ATPase pump subunits is a heterogeneous disease with a…”
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Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1genes by Elhayek, Donia, Perez de Nanclares, Gustavo, Chouchane, Slaheddine, Hamami, Saber, Mlika, Adnène, Troudi, Monia, Leban, Nadia, Ben Romdane, Wafa, Gueddiche, Mohamed Neji, El Amri, Féthi, Mrabet, Samir, Ben Chibani, Jemni, Castaño, Luis, Haj Khelil, Amel, Ariceta, Gema

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Acute polyradiculoneuropathy in children: the Kairouan pediatric department experience. Report of 22 cases by Amri, Fethi, Habboul, Zakia, Troudi, Monia, Ghribi, M, Guedhami, Hamdi, Khattat, Nizar

“…Guillain-Barre Syndrome (GBS) is an acute polyradidulonevritis which is primitive inflammatory and demyelinisant. It represents the most frequent cause of…”
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