DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens

Cholesterol 25-hydroxylase is a metabolic switch to constrain T cell-mediated inflammation in the skin.

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Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy associated with L29P and IVS9-1G>C compound heterozygous autoimmune regulator gene mutations.

Journal of internal medicine·2007

Detailed mapping of the ERG-ETS2 interval of human chromosome 21 and comparison with the region of conserved synteny on mouse chromosome 16.

Gene·2003

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I.

Neurology·2003

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency.

Human genetics·2001

APECED mutations in the autoimmune regulator (AIRE) gene.

Human mutation·2001

Ultra-Widefield OCT Mapping of Foveal and Optic Nerve Head Topography Within Posterior Staphyloma in Pathologic Myopia.

American journal of ophthalmology·2026

Regeneration and Replacement of the Corneal Endothelium: Advances in Cell Therapy, Tissue Engineering, Molecular and Pharmacologic Strategies.

American journal of ophthalmology·2026

Recurrence of Hypertropia in Sagging Eye Syndrome.

American journal of ophthalmology·2026

Impact of Botulinum Toxin on Ocular Surface Parameters in Patients with Orbicularis Spasm: A Systematic Review and Meta-Analysis.

American journal of ophthalmology·2026

Visual performance of a refractive extended depth of field intraocular lens in monovision and emmetropic settings.

American journal of ophthalmology·2026

Cumulative clinical risk factor burden stratifies the need for additional retinal intervention after laser retinopexy for retinal tears.

American journal of ophthalmology·2026

Congruency of exosome-mediated blood-brain barrier dysfunction by activation of Na/K-ATPase in obstructive sleep apnea and Alzheimer's disease.

Cellular and molecular biology (Noisy-le-Grand, France)·2026

Apolipoprotein E2/2 (APOE2/2) Genotype Is Associated With Reduced Choroidal Thickness.

Investigative ophthalmology & visual science·2026

Choroidal Vascular Remodeling After Loading Injections of Faricimab in Diabetic Macular Edema.

Translational vision science & technology·2026

Ultra-Widefield OCTA Mapping of Epiretinal Macrophage-Like Cells in Patients With Retinal Vein Occlusion.

Translational vision science & technology·2026

Clinical Features of Acquired Esotropia and Surgical Management in a Real-World Cohort of Myopic Patients.

Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society·2026

Indocyanine green angiography in uveitis.

Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society·2026

Related Experiment Videos

DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens

Related Concept Videos

Cholesterol 25-hydroxylase is a metabolic switch to constrain T cell-mediated inflammation in the skin.

Recurrent herpes simplex virus infection in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy associated with L29P and IVS9-1G>C compound heterozygous autoimmune regulator gene mutations.

Detailed mapping of the ERG-ETS2 interval of human chromosome 21 and comparison with the region of conserved synteny on mouse chromosome 16.

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I.

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency.

APECED mutations in the autoimmune regulator (AIRE) gene.

Ultra-Widefield OCT Mapping of Foveal and Optic Nerve Head Topography Within Posterior Staphyloma in Pathologic Myopia.

Regeneration and Replacement of the Corneal Endothelium: Advances in Cell Therapy, Tissue Engineering, Molecular and Pharmacologic Strategies.

Recurrence of Hypertropia in Sagging Eye Syndrome.

Impact of Botulinum Toxin on Ocular Surface Parameters in Patients with Orbicularis Spasm: A Systematic Review and Meta-Analysis.

Visual performance of a refractive extended depth of field intraocular lens in monovision and emmetropic settings.

Cumulative clinical risk factor burden stratifies the need for additional retinal intervention after laser retinopexy for retinal tears.

Congruency of exosome-mediated blood-brain barrier dysfunction by activation of Na/K-ATPase in obstructive sleep apnea and Alzheimer's disease.

Apolipoprotein E2/2 (APOE2/2) Genotype Is Associated With Reduced Choroidal Thickness.

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Ultra-Widefield OCTA Mapping of Epiretinal Macrophage-Like Cells in Patients With Retinal Vein Occlusion.

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DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens

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