Eva Orzan

A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment

Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

Newborn Hearing Screening — A Silent Revolution

Clinical efficacy and side effects of antimalarials in systemic lupus erythematosus: a systematic review

Structural and Functional Diversity of Connexin Genes in the Mouse and Human Genome

Thymoquinone and its therapeutic potentials

A genotype-phenotype correlation for GJB2 (connexin 26) deafness

The protective role of thymoquinone in the prevention of gentamicin ototoxicity

Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins

Sensorineural hearing loss in children

A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

Rhesus monkeys for a nonhuman primate model of cytomegalovirus infections

Chloroquine gestational use in systemic lupus erythematosus: assessing the risk of child ototoxicity by pure tone audiometry

Molecular Genetics of Hearing Loss

Immune Correlates of Protection Against Human Cytomegalovirus Acquisition, Replication, and Disease

The “Silent” Global Burden of Congenital Cytomegalovirus

Clinical Practice Guideline: Sudden Hearing Loss (Update)

Human Cytomegalovirus Glycoprotein B Nucleoside-Modified mRNA Vaccine Elicits Antibody Responses with Greater Durability and Breadth than MF59-Adjuvanted gB Protein Immunization

Genetics of Sensory Mechanotransduction

Global Problem of Drug‐Induced Hearing Loss

Molecular Genetics Applied to Clinical Practice: The Cx26 Hearing Impairment

Early Primary Cytomegalovirus Infection in Pregnancy: Maternal Hyperimmunoglobulin Therapy Improves Outcomes Among Infants at 1 Year of Age

Cx26 deafness: mutation analysis and clinical variability