Robert M. Verdijk

Phenotypic consequences of a novel SCO2 gene mutation.

TP53 mutation analysis of malignant peripheral nerve sheath tumors.

A case of adult Pompe disease presenting with severe fatigue and selective involvement of type 1 muscle fibers.

Histopathologic, immunohistochemical, ultrastructural, and cytogenetic analysis of oncocytic uveal melanoma.

COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux.

β-Amyloid Precursor Protein and Ubiquitin Immunohistochemistry Aid in the Evaluation of Infant Autopsy Eyes With Abusive Head Trauma.

Lack of robust satellite cell activation and muscle regeneration during the progression of Pompe disease.

On the Classification and Grading of Medulloepithelioma of the Eye.

Sex Chromosome Analysis of Postmortem Corneal Endothelium After Sex-Mismatch Descemet Membrane Endothelial Keratoplasty.

Histopathologic Features of Descemet Membrane Endothelial Keratoplasty Graft Remnants, Folds, and Detachments.

Persistent Retinal Iron in Abusive Head Trauma.

Three Cases of Erdheim-Chester Disease With Intraocular Manifestations: Imaging and Histopathology Findings of a Rare Entity.

Outcome and Histopathology of Secondary Penetrating Keratoplasty Graft Failure Managed by Descemet Membrane Endothelial Keratoplasty.

Genetic evolution of uveal melanoma guides the development of an inflammatory microenvironment.

Targeting of the MAPK and AKT pathways in conjunctival melanoma shows potential synergy.

Intra-ocular diathermy forceps.

Genetic Background of Iris Melanomas and Iris Melanocytic Tumors of Uncertain Malignant Potential.

Atypical Presentation of Iridocorneal Endothelial Syndrome With Band Keratopathy but No Corneal Edema Managed With Descemet Membrane Endothelial Keratoplasty.

Reply.

Absence of Intraocular Lymphatic Vessels in Uveal Melanomas with Extrascleral Growth.

Aberrant MicroRNA Expression and Its Implications for Uveal Melanoma Metastasis.

Soluble HLA in the Aqueous Humour of Uveal Melanoma Is Associated with Unfavourable Tumour Characteristics.

Aqueous Humor Biomarkers Identify Three Prognostic Groups in Uveal Melanoma.

MicroRNA Profiling in Benign and Malignant Conjunctival Melanocytic Lesions.

-Associated Dystrophies: Clinical, Genetic, and Histopathological Features.

Ileocolic Intussusception as the Presenting Symptom of Primary Enteric Varicella-Zoster Virus Infection in a 7-Month-Old Infant.

Persistent Laryngeal Swelling Caused by Primary Intralymphatic Histiocytosis.

Transient Expression of Lymphatic Markers in Retrobulbar Intraconal Orbital Vasculature During Fetal Development.

Spectrum of histiocytic neoplasms associated with diverse haematological malignancies bearing the same oncogenic mutation.

No Evidence of Varicella-Zoster Virus Infection in Temporal Artery Biopsies of Anterior Ischemic Optic Neuropathy Patients With and Without Giant Cell Arteritis.

Histopathological and Molecular Features of a Conjunctival Caruncular Deep Penetrating Nevus.

Prognostic value of promoter mutations in conjunctival melanomas in addition to clinicopathological features.

Spliceosome Mutations in Uveal Melanoma.

Involvement of mutant and wild-type CYSLTR2 in the development and progression of uveal nevi and melanoma.