IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases von Tauber, Marie, Bal, Elodie, Pei, Xue-Yuan, Madrange, Marine, Khelil, Amel, Sahel, Houria, Zenati, Akila, Makrelouf, Mohamed, Boubridaa, Khaled, Chiali, Amel, Smahi, Naima, Otsmane, Farida, Bouajar, Bakar, Marrakchi, Slaheddine, Turki, Hamida, Bourrat, Emmanuelle, Viguier, Manuelle, Hamel, Yamina, Bachelez, Hervé, Smahi, Asma

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Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino ac... von Haydar, Sara, Grigorescu, Florin, Vintilă, Mădălina, Cogne, Yannick, Lautier, Corinne, Tutuncu, Yildiz, Brun, Jean Frederic, Robine, Jean Marie, Pugeat, Michel, Normand, Christophe, Poucheret, Patrick, Gheorghiu, Monica Livia, Georgescu, Carmen, Badiu, Corin, Băculescu, Nicoleta, Renard, Eric, Ylli, Dorina, Badiou, Stephanie, Sutra, Thibault, Cristol, Jean Paul, Mercier, Jacques, Gomis, Ramon, Macias, Josep Maria, Litvinov, Serghey, Khusnutdinova, Elza, Poiana, Catalina, Pasquali, Renato, Lauro, Davide, Sesti, Giorgio, Prudente, Sabrina, Trischitta, Vincenzo, Tsatsoulis, Agathocles, Abdelhak, Sonia, Barakat, Abdelhamid, Zenati, Akila, Ylli, Agron, Satman, Ilhan, Kanninen, Timo, Rinato, Yves, Missoni, Sasa

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The CD2 isoform of protocadherin‐15 is an essential component of the tip‐link complex in mature auditory hair cells von Pepermans, Elise, Michel, Vincent, Goodyear, Richard, Bonnet, Crystel, Abdi, Samia, Dupont, Typhaine, Gherbi, Souad, Holder, Muriel, Makrelouf, Mohamed, Hardelin, Jean‐Pierre, Marlin, Sandrine, Zenati, Akila, Richardson, Guy, Avan, Paul, Bahloul, Amel, Petit, Christine

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Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome von Abdi, Samia, Bahloul, Amel, Behlouli, Asma, Hardelin, Jean-Pierre, Makrelouf, Mohamed, Boudjelida, Kamel, Louha, Malek, Cheknene, Ahmed, Belouni, Rachid, Rous, Yahia, Merad, Zahida, Selmane, Djamel, Hasbelaoui, Mokhtar, Bonnet, Crystel, Zenati, Akila, Petit, Christine

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A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family von Behlouli, A, Bonnet, C, Abdi, S, Hasbellaoui, M, Boudjenah, F, Hardelin, J.-P, Louha, M, Makrelouf, M, Ammar-Khodja, F, Zenati, A, Petit, C

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Association Between Insulin Resistance and Uric Acid in Hypertension von Otmane, Amel, Makrelouf, Mohamed, Zenati, Akila

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Branched-Chain Amino Acid Database Integrated in MEDIPAD Software as a Tool for Nutritional Investigation of Mediterranean Populations von Haydar, Sara, Paillot, Thomas, Fagot, Christophe, Cogne, Yannick, Fountas, Athanasios, Tutuncu, Yildiz, Vintila, Madalina, Tsatsoulis, Agathocles, Thanh Chi, Pham, Garandeau, Patrick, Chetea, Dan, Badiu, Corin, Gheorghiu, Monica, Ylli, Dorina, Lautier, Corinne, Jarec, Morana, Monnier, Louis, Normand, Christophe, Šarac, Jelena, Barakat, Abdelhamid, Missoni, Sasa, Pugeat, Michel, Poucheret, Patrick, Hanzu, Felicia, Gomis, Ramon, Macias, Josep Maria, Litvinov, Serghey, Khusnutdinova, Elza, Poiana, Catalina, Pasquali, Renato, Lauro, Davide, Sesti, Giorgio, Trischitta, Vincenzo, Abdelhak, Sonia, Zenati, Akila, Ylli, Agron, Satman, Ilhan, Kanninen, Timo, Rinato, Yves, Grigorescu, Florin

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Comparison of three indexes HOMA, QUICKI and TyG to evaluate insulin resistance in type 2 diabetic patients von OTMANE, Amel, ACID, Sadjia, ALLANE, Fahima, MAKRELOUF, Mohamed, ZENATI, Akila

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Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F von Ammar-Khodja, Fatima, Faugère, Valérie, Baux, David, Giannesini, Claire, Léonard, Susana, Makrelouf, Mohamed, Malek, Rahia, Djennaoui, Djamel, Zenati, Akila, Claustres, Mireille, Roux, Anne-Françoise

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Biallelic variants in TMIE and PDE6B genes mimic Usher syndrome von Abdi, Samia, Makrelouf, Mohamed, Rous, Issa Nazim, Ounnoughi, Kheireddine, Zenati, Akila, Petit, Christine, Bonnet, Crystel

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Variations of oxidized ldl and adipocytokine during metabolic syndrome in hypertensive patients von Otmane, Amel, Makrelouf, Mohamed, Zenati, Akila

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EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness von Behlouli, Asma, Bonnet, Crystel, Abdi, Samia, Bouaita, Aïcha, Lelli, Andrea, Hardelin, Jean-Pierre, Schietroma, Cataldo, Rous, Yahia, Louha, Malek, Cheknane, Ahmed, Lebdi, Hayet, Boudjelida, Kamel, Makrelouf, Mohamed, Zenati, Akila, Petit, Christine

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Prevalence of metabolically obese normal weight population in adolescent von BEDDAR, Lamia, CHAA, Abdelmadjid, ZENATI, Akila

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Prévalence de la population de poids normal, métaboliquement obèse, chez l'adolescent [Prevalence of metabolically obese normal weight population in adolescent] von Yasmina GHEDADA, Lamia BEDDAR, Abdelmadjid CHAA, Akila ZENATI

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Branched-chain amino acid database integrated in MEDIPAD software as a tool for nutritional investigation of mediterranean populations von Haydar, Sara, Paillot, Thomas, Fagot, Christophe, Cogne, Yannick, Fountas, Athanasios, Tutuncu, Yildiz, Vintila, Madalina, Tsatsoulis, Agathocles, Chi, Pham Thanh, Garandeau, Patrick, Chetea, Dan, Badiu, Corin, Gheorghiu, Monica, Ylli, Dorina, Lautier, Corinne, Jarec, Morana, Monnier, Louis, Normand, Christophe, Sarac, Jelena, Barakat, Abdelhamid, Missoni, Sasa, Pugeat, Michel, Poucheret, Patrick, Hanzu, Felicia Alexandra, Gomis, Ramon, 1946, Macias, Josep M, Litvinov, Serghey, Khusnutdinova, Elza, Poiana, Catalina, Pasquali, Renato, Lauro, Davide, Sesti, Giorgio, Trischitt, Vincenzo, Abdelhak, Sonia, Zenati, Akila, Ylli, Agron, Satman, Ilhan, Kanninen, Timo, Rinato, Yves, Grigorescu, Floren

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Polymorphisms in NAT2 Gene and Atherosclerosis in an Algerian Population von Khelil, Malika, Zenati, Akila, Makrelouf, Mohamed, Otmane, Amel, Tayebi, Bouchentouf

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Pronostic value of Troponine T High sensitive and NT-proBNP in asymptomatics chronic heamodialysis von Arab, Médina, Zenati, Akila, Labou, Nadia, Missoum, Mohamed, Ainouz, Nouba, Bennoui, Mohamed, Guechi, Zehor

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The CD 2 isoform of protocadherin‐15 is an essential component of the tip‐link complex in mature auditory hair cells von Pepermans, Elise, Michel, Vincent, Goodyear, Richard, Bonnet, Crystel, Abdi, Samia, Dupont, Typhaine, Gherbi, Souad, Holder, Muriel, Makrelouf, Mohamed, Hardelin, Jean‐Pierre, Marlin, Sandrine, Zenati, Akila, Richardson, Guy, Avan, Paul, Bahloul, Amel, Petit, Christine

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Primary evaluation of antioxidant status oligomineral patient with type 2 diabetes Algeria: special interest manganese and chromium von Harani, Hassiba, Otmane, Amel, Makrelouf, Mohamed, Ouadahi, Nacer, Abdi, Arezki, Berrah, Abdelkrim, Zenati, Akila, Alamir, Barkahoum, Koceir, Elhadj Ahmed

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Preliminary evaluation of the antioxidant trace elements in an Algerian patient with type 2 diabetes: special role of manganese and chromium von Harani, Hassiba, Otmane, Amel, Makrelouf, Mohamed, Ouadahi, Nacer, Abdi, Arezki, Berrah, Abdelkrim, Zenati, Akila, Alamir, Barkahoum, Koceir, Elhadj Ahmed

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