Search Results - "Barbouche, Mohamed‐R."

Reversion of neurovirulent mutations, recombination and high intra‐host diversity in vaccine‐derived poliovirus excreted by patients with primary immune deficiency by Ben Salem, Imene, Khemiri, Haifa, Drechsel, Oliver, Arbi, Marwa, Böttcher, Sindy, Mekki, Najla, Ben Fraj, Ilhem, Souiai, Oussama, Yahyaoui, Mahrez, Ben Farhat, Essia, Meddeb, Zina, Touzi, Henda, Ben Mustapha, Imene, BenKahla, Alia, Ouederni, Monia, Barbouche, Mohamed‐R., Diedrich, Sabine, Triki, Henda, Haddad‐Boubaker, Sondes

“…Patients with Primary immunodeficiency (PIDs) may be infected by Polioviruses (PVs), especially when vaccinated with live Oral Polio Vaccine before diagnosis…”
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Le syndrome d'hyper-IgM: 13 observations by BEJAOUI, Mohamed, MELLOULI, Fethi, CHOUANINE, Riadh, DELLAGI, Koussay, BARBOUCHE, Mohamed R

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Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome) by Guirat-Dhouib, Naouel, Baccar, Yemen, Mustapha, Imène Ben, Ouederni, Monia, Chouaibi, Sameh, El Fekih, Nadia, Barbouche, Mohamed Ridha, Fezaa, Bassima, Kouki, Ridha, Hmida, Slama, Mellouli, Fethi, Bejaoui, Mohamed

“…Major histocompatibility complex class II deficiency, also referred to as bare lymphocyte syndrome is a rare primary Immunodeficiency disorder characterized by…”
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The hyper-IgM syndrome: 13 observations by Bejaoui, Mohamed, Mellouli, Fethi, Chouanine, Riadh, Dellagi, Koussay, Barbouche, Mohamed R

“…The hyper-IgM syndrome (HIGM) is a rare hereditary immune deficiency, characterised by a low or nil level of IgG and IgA and a normal or increased level of…”
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