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Genetic spectrum of retinal dystrophies in Tunisia

Scientific reports, 2020-07, Vol.10 (1), p.11199-11199, Article 11199

2020

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Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography

Genes, 2021-11, Vol.12 (11), p.1795

2021

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Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)

Genes, 2019-11, Vol.10 (12), p.953

2019

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Posterior staphylomas in non-highly myopic eyes with retinitis pigmentosa

International ophthalmology, 2020-09, Vol.40 (9), p.2159-2168

2020

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Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, 10 , 953

Genes, 2020-05, Vol.11 (5), p.503

2020

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Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies

Frontiers in cell and developmental biology, 2021-02, Vol.9, p.625560-625560

2021

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Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations

Journal of ophthalmology, 2018-01, Vol.2018, p.1030184-7

2018

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Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian population

Journal of translational medicine, 2012-11, Vol.10 (S3), p.P21-P21, Article P21

2012

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Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

BMC genomics, 2024-08, Vol.25 (1), p.787

2024

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OCT-angiography assessing quiescent and active choroidal neovascularization in retinitis pigmentosa associated with PRPH2 pathogenic variant

European journal of ophthalmology, 2022-07, Vol.32 (4), p.NP98-NP102

2022

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Identifying mutations in Tunisian families with retinal dystrophy

Scientific reports, 2016-11, Vol.6 (1), p.37455-11, Article 37455

2016

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Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria

Human molecular genetics, 2023-01, Vol.32 (4), p.580-594

2023

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Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia

Advances in experimental medicine and biology, 2019, Vol.1185, p.221-226

2019

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Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa

Ophthalmic genetics, 2017-09, Vol.38 (5), p.494-497

2017

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Correction: Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy

Scientific reports, 2017-05, Vol.7 (1), Article 46776

2017

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Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families

International journal of nephrology and renovascular disease, 2010-01, Vol.3 (default), p.85-92

2010

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Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome

La Tunisie medicale, 2021-02, Vol.99 (2), p.302-305

2021

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Complement Component C3 Variant (R102G) and the Risk of Neovascular Age-Related Macular Degeneration in a Tunisian Population

Klinische Monatsblatter fur Augenheilkunde, 2017-04, Vol.234 (4), p.478

2017

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Interleukin-18 Gene Polymorphisms in Tunisian Patients with Inflammatory Bowel Disease

Digestion, 2011-04, Vol.83 (4), p.269-274

2011

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Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy

Scientific reports, 2017-05, Vol.7, p.46776-46776

2017

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Identifying mutations in Tunisian families with retinal dystrophy

Scientific reports, 2016-11, Vol.6 (1), p.37455

2016

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Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian population

Biomarker research, 2014-08, Vol.2 (1), p.15-15, Article 15

2014

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Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography

Genes, 2021, Vol.12 (11)

2021

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Useful Bioactive Compounds from Olive Tree By-Products (Leaves, Branches, Fruits)

Agricultural Waste: Environmental Impact, Useful Metabolites and Energy Production, p.331-358

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Genetic spectrum of retinal dystrophies in Tunisia

Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography

Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)

Posterior staphylomas in non-highly myopic eyes with retinitis pigmentosa

Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, 10 , 953

Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies

Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations

Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian population

Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism

OCT-angiography assessing quiescent and active choroidal neovascularization in retinitis pigmentosa associated with PRPH2 pathogenic variant

Identifying mutations in Tunisian families with retinal dystrophy

Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria

Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia

Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa

Correction: Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy

Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families

Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome

Complement Component C3 Variant (R102G) and the Risk of Neovascular Age-Related Macular Degeneration in a Tunisian Population

Interleukin-18 Gene Polymorphisms in Tunisian Patients with Inflammatory Bowel Disease

Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy

Identifying mutations in Tunisian families with retinal dystrophy

Vascular endothelial growth factor genetic polymorphisms and susceptibility to age-related macular degeneration in Tunisian population

Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography

Useful Bioactive Compounds from Olive Tree By-Products (Leaves, Branches, Fruits)

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