Prevalence of mental retardation in patients with hereditary retinoblastoma

Light therapy: is it safe for the eyes?

Acta psychiatrica Scandinavica·2017

3D Orbital Reconstruction in a Patient with Microphthalmos and a Large Orbital Cyst-A Case Report.

Ophthalmic genetics·2016

Comparing the effectiveness and costs of Bevacizumab to Ranibizumab in patients with Diabetic Macular Edema: a randomized clinical trial (the BRDME study).

BMC ophthalmology·2015

Detection of calcifications in retinoblastoma using gradient-echo MR imaging sequences: comparative study between in vivo MR imaging and ex vivo high-resolution CT.

AJNR. American journal of neuroradiology·2014

Multicenter evaluation of the Sepsityper™ extraction kit and MALDI-TOF MS for direct identification of positive blood culture isolates using the BD BACTEC™ FX and VersaTREK(®) diagnostic blood culture systems.

Journal of applied microbiology·2014

Fasting proinsulin levels are significantly associated with 20 year cancer mortality rates. The Hoorn Study.

Diabetologia·2013

Late onset retinoblastoma in a child with 13 q deletion syndrome.

Ophthalmic genetics·2026

Retinitis Pigmentosa and erythrocytic microcytosis related to hypomorphic variants in the TRNT1 gene.

Ophthalmic genetics·2026

Patient- and caregiver-reported outcomes in Bardet-Biedl syndrome: a scoping review.

Ophthalmic genetics·2026

Anterior segment dysgenesis with bilateral acorea and microphthalmia associated with compound heterozygous FOXE3 pathogenic variants: outcomes after optical iridectomy.

Ophthalmic genetics·2026

Norrie disease with asymmetric retinal severity associated with novel NDP variants.

Ophthalmic genetics·2026

An unusual segmental retinal venous abnormality detected during retinopathy of prematurity screening in an infant with a PAX2 variant.

Ophthalmic genetics·2026

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Human genetics·2026

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Diagnostics (Basel, Switzerland)·2026

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Drug delivery·2026

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

Frontiers in plant science·2026

Rapid and Sensitive Detection of USP26 Cluster Variants Based on CRISPR/Cas12a.

Human mutation·2026

Integrative long-read sequencing, RNA-seq and machine learning framework characterizes and predicts autosomal silencing in unbalanced X-autosome translocations.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

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Prevalence of mental retardation in patients with hereditary retinoblastoma

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Light therapy: is it safe for the eyes?

3D Orbital Reconstruction in a Patient with Microphthalmos and a Large Orbital Cyst-A Case Report.

Comparing the effectiveness and costs of Bevacizumab to Ranibizumab in patients with Diabetic Macular Edema: a randomized clinical trial (the BRDME study).

Detection of calcifications in retinoblastoma using gradient-echo MR imaging sequences: comparative study between in vivo MR imaging and ex vivo high-resolution CT.

Multicenter evaluation of the Sepsityper™ extraction kit and MALDI-TOF MS for direct identification of positive blood culture isolates using the BD BACTEC™ FX and VersaTREK(®) diagnostic blood culture systems.

Fasting proinsulin levels are significantly associated with 20 year cancer mortality rates. The Hoorn Study.

Late onset retinoblastoma in a child with 13 q deletion syndrome.

Retinitis Pigmentosa and erythrocytic microcytosis related to hypomorphic variants in the TRNT1 gene.

Patient- and caregiver-reported outcomes in Bardet-Biedl syndrome: a scoping review.

Anterior segment dysgenesis with bilateral acorea and microphthalmia associated with compound heterozygous FOXE3 pathogenic variants: outcomes after optical iridectomy.

Norrie disease with asymmetric retinal severity associated with novel NDP variants.

An unusual segmental retinal venous abnormality detected during retinopathy of prematurity screening in an infant with a PAX2 variant.

Interobserver reliability and digital morphometric characterization of constitutional chromosomal heteromorphisms in clinical cytogenetics.

Functional Validation of a CC2D2A Non-Canonical Splice-Site Variant Supports Prenatal Molecular Testing in Joubert Syndrome.

Overcoming the nuclear barrier in nonviral gene therapy: mechanisms, carrier design, and translational perspectives on NLS peptide and DNA targeting sequence strategies.

Structural defects in male meiotic cell division lead to reproductive genome instability and disturbed microsporogenesis in banana (Musa spp.).

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Prevalence of mental retardation in patients with hereditary retinoblastoma

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