Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 5
1947 10
1948 2
1949 3
1950 2
1951 4
1952 3
1953 1
1954 1
1955 2
1956 2
1958 1
1959 4
1960 2
1961 1
1962 2
1963 2
1964 7
1965 5
1966 6
1967 7
1968 8
1969 12
1970 6
1971 9
1972 6
1973 6
1974 12
1975 13
1976 14
1977 18
1978 11
1979 4
1980 1
1981 6
1982 6
1983 8
1984 6
1985 5
1986 6
1987 4
1988 4
1989 4
1990 7
1991 8
1992 8
1993 4
1994 6
1995 7
1996 8
1997 8
1998 8
1999 13
2000 16
2001 25
2002 23
2003 20
2004 21
2005 22
2006 22
2007 29
2008 19
2009 26
2010 29
2011 43
2012 31
2013 40
2014 42
2015 35
2016 39
2017 35
2018 27
2019 39
2020 52
2021 64
2022 71
2023 84
2024 22

Text availability

Article attribute

Article type

Publication date

Search Results

1,062 results

Results by year

Filters applied: . Clear all
Page 1
Alport Syndrome: Achieving Early Diagnosis and Treatment.
Kashtan CE. Kashtan CE. Am J Kidney Dis. 2021 Feb;77(2):272-279. doi: 10.1053/j.ajkd.2020.03.026. Epub 2020 Jul 22. Am J Kidney Dis. 2021. PMID: 32712016 Review.
Alport syndrome is a genetically and phenotypically heterogeneous disorder of glomerular, cochlear, and ocular basement membranes resulting from mutations in the collagen IV genes COL4A3, COL4A4, and COL4A5. Alport syndrome can be transmitted as an X-linked, …
Alport syndrome is a genetically and phenotypically heterogeneous disorder of glomerular, cochlear, and ocular basement membranes resulting …
Wolfram Syndrome: Diagnosis, Management, and Treatment.
Urano F. Urano F. Curr Diab Rep. 2016 Jan;16(1):6. doi: 10.1007/s11892-015-0702-6. Curr Diab Rep. 2016. PMID: 26742931 Free PMC article. Review.
Although there are currently no effective treatments that can delay or reverse the progression of Wolfram syndrome, the use of careful clinical monitoring and supportive care can help relieve the suffering of patients and improve their quality of life. ...
Although there are currently no effective treatments that can delay or reverse the progression of Wolfram syndrome, the use of careful clini …
Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development.
Mustillo PJ, Sullivan KE, Chinn IK, Notarangelo LD, Haddad E, Davies EG, de la Morena MT, Hartog N, Yu JE, Hernandez-Trujillo VP, Ip W, Franco J, Gambineri E, Hickey SE, Varga E, Markert ML. Mustillo PJ, et al. J Clin Immunol. 2023 Feb;43(2):247-270. doi: 10.1007/s10875-022-01418-y. Epub 2023 Jan 17. J Clin Immunol. 2023. PMID: 36648576 Free PMC article. Review.
Current practices vary widely regarding the immunological work-up and management of patients affected with defects in thymic development (DTD), which include chromosome 22q11.2 microdeletion syndrome (22q11.2del) and other causes of DiGeorge syndrome (DGS) and coloboma, heart def …
Current practices vary widely regarding the immunological work-up and management of patients affected with defects in thymic development (DT …
Anosmia: Differential diagnosis, evaluation, and management.
Scangas GA, Bleier BS. Scangas GA, et al. Am J Rhinol Allergy. 2017 Jan 1;31(1):3-7. doi: 10.2500/ajra.2017.31.4403. Am J Rhinol Allergy. 2017. PMID: 28234141 Review.
Outcomes studies have highlighted the profound negative impact of anosmia and parosmia on the overall quality of life. The National Institute on Deafness and Other Communication Disorders estimates that 1.4% of the United States population experiences chronic olfactory dys …
Outcomes studies have highlighted the profound negative impact of anosmia and parosmia on the overall quality of life. The National Institut …
Prenatal diagnosis.
Kabra M. Kabra M. Indian J Pediatr. 2003 Jan;70(1):81-5. doi: 10.1007/BF02722749. Indian J Pediatr. 2003. PMID: 12619957 Review.
Ethical issues are already around regarding prenatal testing for disabilities like deafness and late onset disorders. The present communication is an effort to present the clinician's perspective of prenatal diagnosis....
Ethical issues are already around regarding prenatal testing for disabilities like deafness and late onset disorders. The present com …
Newborn cytomegalovirus screening: is this the new standard?
Gantt S. Gantt S. Curr Opin Otolaryngol Head Neck Surg. 2023 Dec 1;31(6):382-387. doi: 10.1097/MOO.0000000000000925. Epub 2023 Oct 11. Curr Opin Otolaryngol Head Neck Surg. 2023. PMID: 37820202 Review.
PURPOSE OF REVIEW: Congenital cytomegalovirus infection (cCMV) is a major cause of childhood hearing loss and neurodevelopmental delay. ...SUMMARY: Targeted screening is widely recommended as standard of care, while universal screening is less common but is progress …
PURPOSE OF REVIEW: Congenital cytomegalovirus infection (cCMV) is a major cause of childhood hearing loss and neurodevelopmental dela …
Impact of COVID-19 on diagnosis and management of newborn hearing loss.
Tu LJ, Benchetrit L, Glovsky CK, Cohen MS. Tu LJ, et al. Int J Pediatr Otorhinolaryngol. 2023 Jul;170:111598. doi: 10.1016/j.ijporl.2023.111598. Epub 2023 May 13. Int J Pediatr Otorhinolaryngol. 2023. PMID: 37207373 Free PMC article.
INTRODUCTION: The COVID-19 pandemic has caused unexpected disruptions in patient care, including adherence to the Early Hearing Detection and Intervention (EHDI) 1-3-6 guidelines. ...METHODS: Retrospective review was performed for all patients who did not pass NHS at two t …
INTRODUCTION: The COVID-19 pandemic has caused unexpected disruptions in patient care, including adherence to the Early Hearing Detec …
Clinical Practice Guideline: Immunotherapy for Inhalant Allergy.
Gurgel RK, Baroody FM, Damask CC, Mims JW, Ishman SL, Baker DP Jr, Contrera KJ, Farid FS, Fornadley JA, Gardner DD, Henry LR, Kim J, Levy JM, Reger CM, Ritz HJ, Stachler RJ, Valdez TA, Reyes J, Dhepyasuwan N. Gurgel RK, et al. Otolaryngol Head Neck Surg. 2024 Mar;170 Suppl 1:S1-S42. doi: 10.1002/ohn.648. Otolaryngol Head Neck Surg. 2024. PMID: 38408152
Specific goals of the guideline are to optimize patient care, promote safe and effective therapy, reduce unjustified variations in care, and reduce the risk of harm. ...The statements in this guideline are not intended to limit or restrict care provide …
Specific goals of the guideline are to optimize patient care, promote safe and effective therapy, reduce unjustified variation …
Neonatal hearing screening.
Oudesluys-Murphy AM, van Straaten HL, Bholasingh R, van Zanten GA. Oudesluys-Murphy AM, et al. Eur J Pediatr. 1996 Jun;155(6):429-35. doi: 10.1007/BF01955176. Eur J Pediatr. 1996. PMID: 8789756 Free article. Review.
Severe congenital hearing impairment is an important handicap affecting 0.1% of live-born infants and 1%-2% of graduates of Neonatal Intensive Care Units. The prognosis for intellectual, emotional, language and speech development in the hearing-impaired child is improved w …
Severe congenital hearing impairment is an important handicap affecting 0.1% of live-born infants and 1%-2% of graduates of Neonatal Intensi …
Consensus clinical management guidelines for Alstrom syndrome.
Tahani N, Maffei P, Dollfus H, Paisey R, Valverde D, Milan G, Han JC, Favaretto F, Madathil SC, Dawson C, Armstrong MJ, Warfield AT, Düzenli S, Francomano CA, Gunay-Aygun M, Dassie F, Marion V, Valenti M, Leeson-Beevers K, Chivers A, Steeds R, Barrett T, Geberhiwot T. Tahani N, et al. Orphanet J Rare Dis. 2020 Sep 21;15(1):253. doi: 10.1186/s13023-020-01468-8. Orphanet J Rare Dis. 2020. PMID: 32958032 Free PMC article.
The rarity and complexity of the syndrome and the lack of expertise can lead to delayed diagnosis, misdiagnosis and inadequate care. Multidisciplinary and multiprofessional teams of experts are essential for the management of patients with ALMS, as early diagnosis and inte …
The rarity and complexity of the syndrome and the lack of expertise can lead to delayed diagnosis, misdiagnosis and inadequate care. …
1,062 results