Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sonia Talbi"'
Autor:
Crystel Bonnet, Sonia Talbi, Christine Petit, Fatima Ammar-Khodja, Merieme Djebbar, Farid Boudjenah, Malika Dahmani, Sofiane Ouhab
Publikováno v:
International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, 2020, 129, pp.109772. ⟨10.1016/j.ijporl.2019.109772⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2020, 129, pp.109772. ⟨10.1016/j.ijporl.2019.109772⟩
International Journal of Pediatric Otorhinolaryngology, 2020, 129, pp.109772. ⟨10.1016/j.ijporl.2019.109772⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2020, 129, pp.109772. ⟨10.1016/j.ijporl.2019.109772⟩
International audience; Hereditary distal renal tubular acidosis (dRTA) is a rare disorder characterized by metabolic acidosis due to impaired renal acid excretion. To date, three genes (ATP6V1B1, ATP6V0A4 and SLC4A1) have been reported to be respons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf21a41cd50ecbc1dd4742ae31040a43
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219608
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219608
Autor:
Crystel Bonnet, Sonia Talbi, Christine Petit, Mohammed Tahar Mansouri, Farid Boudjenah, Fatima Ammar Khodja
Publikováno v:
International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, 2019, 124, pp.157-160. ⟨10.1016/j.ijporl.2019.05.036⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2019, 124, pp.157-160. ⟨10.1016/j.ijporl.2019.05.036⟩
International Journal of Pediatric Otorhinolaryngology, 2019, 124, pp.157-160. ⟨10.1016/j.ijporl.2019.05.036⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2019, 124, pp.157-160. ⟨10.1016/j.ijporl.2019.05.036⟩
International audience; Introduction: DFNB1, caused by mutations of GJB2 or GJB6, is the most prevalent genetic form of nonsyndromic (i.e., isolated) congenital deafness in countries located around the Mediterranean Sea. Because some mutations are re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b30a753cbbc743fc44529d1c3e27103
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219629
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219629
Autor:
Fatima Ammar-Khodja, Christine Petit, Malika Dahmani, Fabienne Wong Jun Tai, Malek Louha, Jean-Pierre Hardelin, Farid Boudjenah, Zied Riahi, Crystel Bonnet, Sonia Talbi
Publikováno v:
International Journal of Pediatric Otorhinolaryngology
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2018, 112, pp.1-5. ⟨10.1016/j.ijporl.2018.06.012⟩
International Journal of Pediatric Otorhinolaryngology, 2018, 112, pp.1-5. ⟨10.1016/j.ijporl.2018.06.012⟩
International Journal of Pediatric Otorhinolaryngology, Elsevier, 2018, 112, pp.1-5. ⟨10.1016/j.ijporl.2018.06.012⟩
International Journal of Pediatric Otorhinolaryngology, 2018, 112, pp.1-5. ⟨10.1016/j.ijporl.2018.06.012⟩
International audience; Background: Consanguinity rate is high in Algeria, and the population is thus at high risk for genetic diseases transmitted on an autosomal recessive mode. Inherited congenital hearing impairment (HI) is a highly heterogeneous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15100fce6bc1958062d23c995bb02a78
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219637
https://hal-pasteur.archives-ouvertes.fr/pasteur-03219637