Benign hereditary chorea, not only chorea: a family case presentation

por Koht, Jeanette, Løstegaard, Sven Olav, Wedding, Iselin, Vidailhet, Marie, Louha, Malek, Tallaksen, Chantal ME
Publicado 2016

Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

por Ammar-Khodja, Fatima, Bonnet, Crystel, Dahmani, Malika, Ouhab, Sofiane, Lefèvre, Gaelle M, Ibrahim, Hassina, Hardelin, Jean-Pierre, Weil, Dominique, Louha, Malek, Petit, Christine
Publicado 2015

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness

por 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
Publicado 2014

Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome

por 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
Publicado 2016

Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients

por Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Lahbib, Saida, Bouyacoub, Yosra, Bechraoui, Rym, Marrakchi, Jihène, Hardelin, Jean-Pierre, Louha, Malek, Largueche, Leila, Ben Yahia, Salim, Kheirallah, Moncef, Elmatri, Leila, Besbes, Ghazi, Abdelhak, Sonia, Petit, Christine
Publicado 2015

Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?

por Enaud, Laurent, Hadchouel, Alice, Coulomb, Aurore, Berteloot, Laureline, Lacaille, Florence, Boccon-Gibod, Liliane, Boulay, Vincent, Darcel, Françoise, Griese, Matthias, Linard, Mélinée, Louha, Malek, Renouil, Michel, Rivière, Jean-Pierre, Toupance, Bruno, Verkarre, Virginie, Delacourt, Christophe, de Blic, Jacques
Publicado 2014

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

por Riahi, Zied, Bonnet, Crystel, Zainine, Rim, Louha, Malek, Bouyacoub, Yosra, Laroussi, Nadia, Chargui, Mariem, Kefi, Rym, Jonard, Laurence, Dorboz, Imen, Hardelin, Jean-Pierre, Salah, Sihem Belhaj, Levilliers, Jacqueline, Weil, Dominique, McElreavey, Kenneth, Boespflug, Odile Tanguy, Besbes, Ghazi, Abdelhak, Sonia, Petit, Christine
Publicado 2014