Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Precision Health Database


Precision Health Database|Search|PHGKB

Reproductive and Child Health

Last data update: Nov 29, 2023. (Total: 62229 Documents since 2012)
   dataset      
Filtered By:

Previous    

Records 1 - 30 (of 81 Records)

Next

Query Trace: Hearing Loss Or Hearing Screening Or Congenital Deafness[original query]>>Reviews/Commentaries[Product Type]
A Parent’s Guide to Genetics and Hearing Loss
CDC, 2023
Summary of the Polish Universal Neonatal Hearing Screening Program 2021year review.
Grazyna Greczka et al. Otolaryngologia polska = The Polish otolaryngology 2023 77(1) 1-5
Implementation of Population-Based Genetic Testing of Newborn Infants for Prediction of Hearing Loss in Ontario, Canada
CDC Webinar, April 19, 2023
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
Clabout Thomas et al. Genes 2023 14(1)
Congenital hearing loss: a literature review of the genetic etiology in a Mexican population.
Torre-González Carlos de la et al. Boletin medico del Hospital Infantil de Mexico 2022 79(4) 206-214
Achondroplasia in Latin America: practical recommendations for the multidisciplinary care of pediatric patients.
Llerena Juan et al. BMC pediatrics 2022 22(1) 492
Comprehensive Genomic Sequencing-Based Screening for Hearing Loss in the Neonatal Intensive Care Setting-Is It Time?
Abou Tayoun Ahmad N et al. JAMA network open 2022 5(7) e2220992
Comprehensive Genomic Sequencing–Based Screening for Hearing Loss in the Neonatal Intensive Care Setting—Is It Time?
AN Abou Tayoun, JAMA Network Open, July 11, 2022
Genetics of Childhood Hearing Loss.
Mitchell Calli Ober et al. Otolaryngologic clinics of North America 2021 54(6) 1081-1092
Genetic screening techniques and diseases for neonatal genetic diseases.
Han Lianshu et al. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2021 50(4) 429-435
Newborn Hearing Screening Can Improve Reading Skills
CDC, October 2021
Universal newborn hearing screening in the Italian Region of Sicily in 2018.
Ferlito Salvatore et al. Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale 2021 41(4) 356-363
Annual Data: Early Hearing Detection and Intervention (EHDI) Program
CDC, July 2021
Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant Patients.
Nisenbaum Eric et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 42(1) 180-187
Computational Audiology: New Approaches to Advance Hearing Health Care in the Digital Age.
Wasmann Jan-Willem A et al. Ear and hearing 2021
Association of clinical droplet digital PCR and next-generation sequencing-based copy number variant assays with hearing loss: current status and future prospects.
Rentas Stefan et al. Expert review of molecular diagnostics 2021 Feb
Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review.
Zhan Kevin Y et al. Journal of otology 2021 Jan 16(1) 40-46
Perspectives of newborn hearing screening in resource constrained settings.
Das Soumyajit et al. Journal of otology 2020 Dec 15(4) 174-177
Screening for GJB2-R143W-Associated Hearing Impairment: Implications for Health Policy and Practice in Ghana.
Adadey Samuel M et al. Public health genomics 2020 Dec 1-6
The Many Faces of DFNB9: Relating OTOF Variants to Hearing Impairment.
Vona Barbara et al. Genes 2020 Nov 11(12)
Public health policy-making for hearing loss: stakeholders' evaluation of a novel eHealth tool.
Dritsakis Giorgos et al. Health research policy and systems 2020 Oct 18(1) 125
Evaluation of guidelines for universal newborn hearing screening programs.
Spivak Lynn et al. Developmental medicine and child neurology 2020 Oct
The Importance of Early Genetic Diagnostics of Hearing Loss in Children.
Božanic Urbancic Nina et al. Medicina (Kaunas, Lithuania) 2020 Sep 56(9)
Using biomarkers in acute medicine to prevent hearing loss: should this require specific consent?
Coulson-Smith Peta et al. Journal of medical ethics 2020 Jul
Genetic testing in the acute setting: a round table discussion.
McDermott John Henry et al. Journal of medical ethics 2020 Jul
Artificial Intelligence Applications in Otology: A State of the Art Review.
You Eunice et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2020 Jun 194599820931804
CRISPR/Cas9: targeted genome editing for the treatment of hereditary hearing loss.
Farooq Rimsha et al. Journal of applied genetics 2020 Feb 61(1) 51-65
Reproductive options for families at risk of Osteogenesis Imperfecta: a review.
Zhytnik Lidiia et al. Orphanet journal of rare diseases 2020 May 15(1) 128
Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
Canda Ebru et al. Pediatric health, medicine and therapeutics 2020 11127-133
A Data-informed Public Health Policy-Makers Platform.
Brdaric Dario et al. International journal of environmental research and public health 2020 May 17(9)
TOP