Neonatal Erythroderma: Diagnostic Challenges and the Limitations of Genetic Testing. [PDF]
CureusPhipps J, Popescu O.
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Anterior Segment OCT Features of Cytomegalovirus Endotheliitis Mimicking Graft Rejection After DSAEK: Report of Two Cases and Diagnostic Implications. [PDF]
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From <i>Fusarium solani</i> Keratitis to Full Visual Acuity: A Case of Infection Requiring Multiple Corneal Transplants. [PDF]
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Atypical case of neonatal-onset Gaucher disease type 3b: A case report. [PDF]
Mol Genet Metab RepOnuki T +7 more
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Blaschko-Linear TGM1-nEDD Associated With Mosaic Genome-Wide Uniparental Isodisomy. [PDF]
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Artificial Intelligence and Eye Disease-Bridging Innovation and Clinical Practice. [PDF]
J Clin MedChen H, Arnould L, Grzybowski A.
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The Unfolding of Familial CARD14- Associated Papulosquamous Eruption (CAPE) and a Brief Review. [PDF]
Indian Dermatol Online JShah S, Hegde SS, Inamadar A, Dahe NV.
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Holocarboxylase Synthetase Deficiency: Clinical, Biochemical and Molecular Findings in Five Malaysian Patients Including a Newborn Presenting as Collodion Baby. [PDF]
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In vitro experimental study of MC-PMMA containing vancomycin for the prevention of infection in open bone defects. [PDF]
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Enhancing Diagnostic Precision in Fuchs Dystrophy: Comparative Evaluation of REVO HR and FC130 OCT Systems. [PDF]
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