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

Year Number of Results
1990 1
1992 4
1993 1
1996 4
1998 3
1999 3
2000 4
2001 5
2002 12
2003 13
2004 5
2005 7
2006 4
2007 8
2008 5
2009 10
2010 5
2011 10
2012 1
2013 6
2014 7
2015 5
2016 7
2017 7
2018 2
2019 1
2020 5
2021 7
2022 6
2023 3
2024 1

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151 results

Results by year

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Page 1
Educational Case: Platelet refractoriness.
Griffith AJ, Rose WN. Griffith AJ, et al. Acad Pathol. 2022 May 12;9(1):100015. doi: 10.1016/j.acpath.2022.100015. eCollection 2022. Acad Pathol. 2022. PMID: 35600743 Free PMC article. No abstract available.
Atypical and ultra-rare Usher syndrome: a review.
Nolen RM, Hufnagel RB, Friedman TB, Turriff AE, Brewer CC, Zalewski CK, King KA, Wafa TT, Griffith AJ, Brooks BP, Zein WM. Nolen RM, et al. Among authors: griffith aj. Ophthalmic Genet. 2020 Oct;41(5):401-412. doi: 10.1080/13816810.2020.1747090. Epub 2020 May 6. Ophthalmic Genet. 2020. PMID: 32372680 Free PMC article. Review.
Genetic Hearing Loss Associated With Autoinflammation.
Nakanishi H, Prakash P, Ito T, Kim HJ, Brewer CC, Harrow D, Roux I, Hosokawa S, Griffith AJ. Nakanishi H, et al. Among authors: griffith aj. Front Neurol. 2020 Mar 5;11:141. doi: 10.3389/fneur.2020.00141. eCollection 2020. Front Neurol. 2020. PMID: 32194497 Free PMC article. Review.
Unresolved questions regarding human hereditary deafness.
Rehman AU, Friedman TB, Griffith AJ. Rehman AU, et al. Among authors: griffith aj. Oral Dis. 2017 Jul;23(5):551-558. doi: 10.1111/odi.12516. Epub 2016 Jul 11. Oral Dis. 2017. PMID: 27259978 Free PMC article. Review.
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct.
Roux I, Fenollar-Ferrer C, Lee HJ, Chattaraj P, Lopez IA, Han K, Honda K, Brewer CC, Butman JA, Morell RJ, Martin DM, Griffith AJ. Roux I, et al. Among authors: griffith aj. Hum Genet. 2023 Oct;142(10):1499-1517. doi: 10.1007/s00439-023-02581-x. Epub 2023 Sep 5. Hum Genet. 2023. PMID: 37668839 Free PMC article.
Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy.
Faridi R, Yousaf R, Gu S, Inagaki S, Turriff AE, Pelstring K, Guan B, Naik A, Griffith AJ, Adadey SM, Aboagye ET, Awandare GA, Morell RJ, Tsilou E, Noyes AG, Sulmonte LAG, Wonkam A, Schrauwen I, Leal SM, Azaiez H, Brewer CC, Riazuddin S, Hufnagel RB, Hoa M, Zein WM, de Dios JK, Friedman TB. Faridi R, et al. Among authors: griffith aj. Clin Genet. 2023 Jun;103(6):699-703. doi: 10.1111/cge.14312. Epub 2023 Mar 13. Clin Genet. 2023. PMID: 36807241
Hereditary hearing loss with thyroid abnormalities.
Choi BY, Muskett J, King KA, Zalewski CK, Shawker T, Reynolds JC, Butman JA, Brewer CC, Stewart AK, Alper SL, Griffith AJ. Choi BY, et al. Among authors: griffith aj. Adv Otorhinolaryngol. 2011;70:43-49. doi: 10.1159/000322469. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358184 Review.
Dissection of the Endolymphatic Sac from Mice.
Honda K, Lee HJ, Griffith AJ, Roux I. Honda K, et al. Among authors: griffith aj. J Vis Exp. 2021 Mar 29;(169):10.3791/62375. doi: 10.3791/62375. J Vis Exp. 2021. PMID: 33843930 Free PMC article.
151 results