about
An Introduction to the Genetics of Normal and Defective HearingGenomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaOutcome predictors of treatment effectiveness for fungal malignant external otitis: a systematic reviewNew trends in rehabilitation of children with ENT disorders.Dose-dependent protection on cisplatin-induced ototoxicity - an electrophysiological study on the effect of three antioxidants in the Sprague-Dawley rat animal model.Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss. A case control studyTEOAE recording protocols revised: data from adult subjects.Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain Anomalies.Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier geneGJB2 mutations and degree of hearing loss: a multicenter study.Uniform mesoporous silica coated iron oxide nanoparticles as a highly efficient, nontoxic MRI T(2) contrast agent with tunable proton relaxivities.Cochlear repair by transplantation of human cord blood CD133+ cells to nod-scid mice made deaf with kanamycin and noise.The eminent anatomists who discovered the upper oesophageal sphincter.Progress in understanding GJB2-linked deafness.Coenzyme Q10 plus Multivitamin Treatment Prevents Cisplatin Ototoxicity in Rats.Tissue engineering and cartilage regeneration for auricular reconstruction.Merkel cell tumour of the external ear. Report of a case.Goldenhar syndrome in association with agenesia of the internal carotid artery.Correlation of adverse effects of cisplatin administration in patients affected by solid tumours: a retrospective evaluationA case-case study on sinonasal cancer prevention: effect from dust reduction in woodworking and risk of mastic/solvents in shoemakingConsiderations on the physiopathological mechanism of inner ear damage induced by intravenous cocaine abuse: cues from a case report.The diagnosis of autoimmune inner ear disease: evidence and critical pitfalls.Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.Rehabilitation and outcome of severe profound deafness in a group of 16 infants affected by congenital cytomegalovirus infection.Vertigo and autoimmunity.Electrode features for hearing preservation and drug delivery strategies.Genetic syndromes involving hearing.Environmental and genetic factors in age-related hearing impairment.The complimentary role of diagnostic and therapeutic endoscopy in foreign body aspiration in children.How to motivate newborn hearing screening in the absence of a national programme: a collaboration between parents and professionals.Endocochlear inflammation in cochlear implant users: case report and literature review.Mastoiditis in adults: a 19-year retrospective study.Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literature.EYA1-related disorders: two clinical cases and a literature review.Temporal bone carcinoma. Current diagnostic, therapeutic, and prognostic concepts.Hearing loss and cognitive decline in older adults: questions and answers.Bilateral chondrosarcoma of the jugular foramen: literature review and personal experience.Aging, cognitive load, dementia and hearing loss.Olfaction deterioration in cognitive disorders in the elderly.Temporal bone carcinoma: a first glance beyond the conventional clinical and pathological prognostic factors.
P50
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P50
description
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Alessandro Martini
@ast
Alessandro Martini
@en
Alessandro Martini
@es
Alessandro Martini
@nl
type
label
Alessandro Martini
@ast
Alessandro Martini
@en
Alessandro Martini
@es
Alessandro Martini
@nl
prefLabel
Alessandro Martini
@ast
Alessandro Martini
@en
Alessandro Martini
@es
Alessandro Martini
@nl
P1006
P214
P1006
P106
P1153
7202003953
P21
P214
P31
P496
0000-0002-2003-6348
P734
P735
P7859
lccn-n97800262