نتایج جستجو برای: newborn hearing screening

تعداد نتایج: 387433  

Journal: :Italian Journal of Pediatrics 2017

Journal: :Archives of Pediatrics & Adolescent Medicine 2008

Journal: :International Journal of Pregnancy & Child Birth 2016

Journal: : 2021

Amaç: Kal?c? i?itme kayb? en s?k görülen konjenital hastal?klardan biridir. ?nsidans?n?n bin canl? do?umda 1-3 aras?nda oldu?u dü?ünülmektedir. Tarama yap?lmazsa kayb?n?n erken 2 ya??nda anla??labildi?i ve bunun da çocu?un geli?imi için oldukça kötü sonuçlar do?urdu?u bildirilmi?tir. Bu çal??mada Sakarya ilindeki hastanelerde 2018 y?l?nda yap?lan tüm yenido?an taramalar?n?n de?erlendirilmesi am...

Journal: :Journal of the American Academy of Audiology 1990
J T Jacobson

The introduction of electrophysiologic measures has provided a renewed interest in the early identification of newborns and infants at risk for hearing loss. To date, 14 states have enacted mandatory legislation for newborn hearing screening, whereas other states have incorporated private and hospital-based programs. Although all state and local programs are inherently different, their common g...

Journal: :BMC Health Services Research 2006
Eva Grill Kai Uus Franz Hessel Linda Davies Rod S Taylor Juergen Wasem John Bamford

BACKGROUND Children with congenital hearing impairment benefit from early detection and management of their hearing loss. These and related considerations led to the recommendation of universal newborn hearing screening. In 2001 the first phase of a national Newborn Hearing Screening Programme (NHSP) was implemented in England. Objective of this study was to assess costs and effectiveness for h...

Journal: :Archives of Disease in Childhood 2015

Journal: :The Southeast Asian journal of tropical medicine and public health 2003
Roy Joseph

Births in Singapore are almost exclusively in hospitals and this is conducive to mass newborn screening. Mass newborn screeningbegan in 1965 for G6PD deficiency and has led to successful eradication of the complicating kernicterus. Screening has also identified the distinct ethnic and sex linked variations in incidence. The predominant molecular abnormality is the Canton variant. Congenital hyp...

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