Výsledky vyhledávání - "Khalil Turki"

Akademický článek

Efficacy and Safety in Retinal Vein Occlusion Treated with at Least Three Consecutive Intravitreal Dexamethasone Implants

Autor: Julia Proença Pina, Khalil Turki, Julien Labreuche, Alain Duhamel, Thi Ha Chau Tran

Publikováno v: Journal of Ophthalmology, Vol 2016 (2016)

Purpose. To evaluate the effects of repeated intravitreal dexamethasone implant (DI) (Ozurdex®) in eyes with macular edema (ME) due to retinal vein occlusion (RVO). Methods. Multicenter observational study including patients who received more than t

Externí odkaz: https://doaj.org/article/ed3391462a1647528b49a382e9d33a3f

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Efficacy and Safety in Retinal Vein Occlusion Treated with at Least Three Consecutive Intravitreal Dexamethasone Implants

Autor: Julien Labreuche, Julia Proença Pina, Thi Ha Chau Tran, Alain Duhamel, Khalil Turki

Publikováno v: Journal of Ophthalmology, Vol 2016 (2016)
Journal of Ophthalmology
Journal of Ophthalmology, Hindawi Publishing Corporation, 2016, ⟨10.1155/2016/6016491⟩
Journal of Ophthalmology, 2016, ⟨10.1155/2016/6016491⟩

Purpose. To evaluate the effects of repeated intravitreal dexamethasone implant (DI) (Ozurdex®) in eyes with macular edema (ME) due to retinal vein occlusion (RVO).Methods. Multicenter observational study including patients who received more than th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f45239267d961b1fd220369fe24b1ba8
https://doaj.org/article/ed3391462a1647528b49a382e9d33a3f

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A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family

Autor: Melek Mnejja, Mariem Ben Said, Ayda Khalfallah, Zeineb Benzina, Ignacio del Castillo, Khalil Turki, Leila Ayedi, Bochra Hakim, Mounira Hmani Aifa, Abdelmonem Ghorbel, Hammadi Ayadi, Ilhem Charfeddine, Saber Masmoudi, Chamseddine Khifagi

Publikováno v: European Journal of Medical Genetics. 54:e535-e541

Autosomal recessive non-syndromic hearing loss (ARNSHL) is a genetically heterogenous disorder with 41 genes so far identified. Among these genes, ESRRB whose mutations are responsible for DFNB35 hearing loss in Pakistani and Turkish families. This g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::455349c487509409a3eb3780be26f8f8
https://doi.org/10.1016/j.ejmg.2011.06.008

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Localization of a Novel Autosomal Recessive Non-syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3-q13.4

Autor: Malika Drira, Houria Dhouib, Ilhem Charfedine, S. Bouaziz, H. Ayadi, I. Ben Rebeh, Jihen Chouchen, Abdelaziz Tlili, S. Masmoudi, Khalil Turki, Zeineb Benzina

Publikováno v: Annals of Human Genetics. 71:271-275

Summary Hereditary hearing impairment is the most genetically heterogeneous trait known in humans. So far, 50 published autosomal recessive non-syndromic hearing impairment (ARNSHI) loci have been mapped, and 23 ARNSHI genes have been identified. Her

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2412a81ca9156413c7f42fe77bb1a0fc
https://doi.org/10.1111/j.1469-1809.2006.00337.x

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A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1

Autor: Mounira Hmani-Aifa, Hammadi Ayadi, Faïza Fakhfekh, Khalil Turki, Peter Söderkvist, Riadh Messaoud, Moncef Khairallah, Salma Ben Salem, Ahmed Rebai, Walid Bouassida, Zeineb Benzina

Publikováno v: Human genetics. 126(4)

Posterior microphthalmia (PM) is a relatively rare autosomal recessive condition with normal anterior segment and small posterior segment resulting in high hyperopia and retinal folding. It is an uncommon subtype of microphthalmia that has been mostl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73656537bd66fd5879743b4628d176ba
https://pubmed.ncbi.nlm.nih.gov/19526372

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