Hearing impairment : audiological management /
edited by Sophie Silva.
- ix, 232 pages : illustrations ; 29 cm.
Includes bibliographical references and index.
CHD7 deficiency in "looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment -- Diminished behavioral and neural sensitivity to sound modulation is associated with moderate developmental hearing loss -- A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart -- Challenges in whole exome sequencing: an example from heredity deafness -- Polymorphisms in toll-like receptors, 2,4, and 9 are highly associated with hearing loss in survivors of bacterial meningitis -- Finding ne genes for non-syndromic hearing loss through an in silico prioritization study -- Molecular epidemiology and functional assessment of novel allelic variants of SLc26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct -- Neuromagnetic index of hemispheric asymmetry prognosticating the outcome of sudden hearing loss -- Hearing loss and hair cell death in mice given the cholesterol-chelating agent hydroxypropyl-β-cyclodextrin -- A novel missense mutation in the connexin30 cause nonsyndromic hearing loss - Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness -- Rescue of inhibitory synapse strength following developmental hearing loss -- The effect of visual cues on difficulty ratings for segregation of musical streams in listeners with impaired hearing -- Congenital sensorineural deafness in Australian stumpy-tail cattle dogs is an autosomal recessive trait that maps to CFA10 -- The p.V371 exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment -- Eye gaze during observation of static faces in deaf people -- Identification and functional study of a new missense mutation in the motor head domain of of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11) -- Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss -- Diaphanous homolog 3 (diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness -- Evaluation of treatment thresholds for unconjugated hyperbilirubinemia in preterm infants: effects on serum bilirubin and on hearing loss? -- Glue ear, hearing loss and IQ: an association moderated by the child's home environment -- Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness -- FGF23 deficiency leads to mixed hearing loss and middle ear malformation in mice -- Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.